#which is a benign bone tumor
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why the fuck does my insurance's website say its over a thousand dollars for an x-ray or ct scan? is that really accurate? i would have to pay for it because I haven't met my deductible yet, but I can't fucking afford that shit right now.
#basically i have something that i think is a osteoma#which is a benign bone tumor#ive had it on my skull for over a decade now#and im starting to get more frequent headaches and stiff neck and tenderness around that area from it#so i thought maybe i should get that checked out#but i cant do that if i gotta pay that much fucking money#also the only solution is surgery and i cant afford that either
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My doctor has given me the award for Weirdest Cyst Ever and I can't wait to get the results back from pathology. But the nurse took it away before I could look at it 😭. I am winning at Weird Cyst.
#ive had this thing for 18 years so it better be weird and i better get a prize for it!#long story but we assumed it was one of my benign bone tumors because it developed when my other tumors developed#and didnt change at all until like maybe 1 year ago#and its a sign of possible cancer when these change as an adult and they need to be removed if possible when they change#it feels and looks like my other tumors: rock hard#so my surgeon was extremely shocked when he went in through my scalp to chissle it off my forehead and it blew up.#it stared coming back so we removed it in-office today with novacaine and cutting directly above jt#but it was literally adhered to my skull!!!#he had to take a metal tool and SCRAPE MY SKULL which was truly the most disturbing sensation/sound#like getting your teeth cleaned BUT IT WAS MY SKULL.#and there i literally a crater where the cyst was because i guess my skull was still growing#and couldnt properly grow with the rock hard cyst putting pressure there?#but it was filled with fluid so its crazy how hard it felt#even though it had only refilled a little bit!!!#its crazy how I was literally the worst person possible to get this cyst because it completely mimiced my bone tumor symptoms lol#other than that it was an atypical place to get those bone tumors since it wasnt by a growth plate#but i also have other tumors that arent by groth plates!!! insane!!!!#it also makes me wonder if i have other cysts that are acting like my bone tumors...#forhead hurty... and im probably not going to be able to raise my eyebrows for a few weeks without pain#but im so happy to be rid of this thing...
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Twilight's Notes: Autopsy Report
Subject: Cheerilee Infection Type: Stage 3, Growler Cause of Death: Malnutrition
Important Notes: Food was provided to the Subject through slats in the door to her observation room. It was noted that she refused any non-meat food items, often smelling provided vegetables and fruit before wandering away in an angry huff. When provided with meat the subject devoured it ravenously. (Additional Note: Fluttershy is still Very distraught by the act of feeding meat to a subject, understandably so. The animals butchered were already dead when it was done, but I admit the act turned my stomach as well.)
Results of the Autopsy of Cheerilee: Pustules had a thicker membrane than what has been found in other Growler subjects, this has been noted in the Growler files under 'Secondary Mutations', Section Four, Pustule Growth. Additionally, the fluid inside had developed a thick consistency, atypical of previous tests on samples taken from the subject while still alive. Potentially a postmortem event similar to bloating and blood coagulation. The Cranial region of the subject shows typical deconstruction of the front of the skull where the largest pustules grow over the eyes. Bone was missing and the brain was protected solely by the thick covering of the pustules themselves. This was noted with previous autopsies as being how popping the facial pustules can be used to kill the infected. Oddly enough, Cheerilee is a unique case- in that her eyes were still present. They were nonfunctional and buried beneath the growths, but she is the only Growler so far to have them still intact. They were pushed back into the remainder of the skull and put pressure on her brain. It was noted this may be the reason for some of the subject's atypical behavior. (Note: Cheerilee struggled to walk in a straight line and frequently ran into the walls. Additionally, she had a total of five seizures in the few weeks she was in stage 3.)
The state of the subject's teeth were abysmal, many of them were chipped or shattered due to aggressive clenching and gnawing on bone. Multiple lesions in the mouth reveal a recurring observation that the sharpened teeth of the infected don't fit right in the mouth and will often cut their cheeks. The manner in which the teeth end up in this state is still debated. (Personal Note: I believe there is magic involved in much of the disease's effects, with the transformation of the teeth being one such magic-affected change.)
Internal organs were in poor condition, showing signs typical of extreme malnutrition. There were also several tumors and cysts found throughout, once again not uncommon in Growler cadavers. However there were less within Cheerilee than in previous subjects. I'm noting this as being likely due to Cheerilee being the shortest-lived Type 1 in my care to date. Aside from the growths- Which were later tested and found to be a mix of benign and cancerous- I discovered something I hadn't noticed before, though I suspect that was a simple oversight on my part. The glands that create saliva were engorged, the pores from which saliva is discharged were wider than normal. This almost certainly explains the thick, excessive saliva that often drips from a Type 1's mouth.
Final Notes: Most findings were either typical, or slightly atypical of the Type 1 infected. Though some new things were discovered, overall the autopsy proved to be more useful in the fact that I obtained a significant number of samples that I can use. I'll be taking these to study and try to find anything the may lead me towards an understanding of the mutagenic properties of the infection. I may also compare the samples to early-stage infected, stage 1s, 2s, and recovered ponies. My goal is not just to understand the infected themselves, but how the disease got to where it is now- Perhaps develop some sort of vaccine, or a cure for those still in the first 1-2 weeks where they can be saved.
I will be adding this file to the autopsy logs for future reference.
#Twilight's Research Notes#not art#mlp infection au#the glow#Just FYI#the infection began officially 5 months ago#it grew out of control around two months ago#so Twilight has had time to research- but things aren't as easy as she'd hoped in the beginning.#partially because of the infection being so mutagenic#partially because she doesn't know what started the infection or who patient zero is
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i’m pretty much through with developing these specific characters (most of the story came about when i was 15-17) but I still love their designs and I certainly wrote some interesting stories about them so I wanted to share it?? lol??
Below the cut is an excerpt from one of these stories, set during the aftermath of the main story, so it might not make much sense. (tw for some described gore and depression.)
Started to get nightmares at the hospital, Kitty wrote. She was discharged after four days. A mild concussion, bruises and the remainder of the dehydration and mild starvation from being in the cage. Everyone else was worse.
Veel had two gashes across her face, one across her nose and one splitting her chin open, and she had a bullet wound in her neck, but horribly, it had healed itself, pushing the bullet out of the puncture and closing into a gnarled, fleshy knob on the side of her throat. Luckily the tumor was benign and got removed in surgery, and the cuts were stitched, but now she had these frankenstein-esque scars, that would probably fade a little, but never really go away.
Anneke had a stab wound from Winghead’s makeshift rebar spear. Luckily there was no tetanus, and Harpy had disappeared through the hole in her side, causing it to begin closing up. By the time they had gotten to the ER, it had regressed to maybe a half inch deep on both sides.
Sunny was fine aside from some bruises. He and Anneke were texting and calling pretty much the entire time she was in the hospital.
Luke’s father, once he wasn’t ingesting a slow but steady supply of antifreeze, stopped seizing and regained his mental abilities, though he remained disorientated and nauseous.
Winghead had several gashes from Harpy, bite marks from the Guests, and his curse mark had turned into a second degree burn. With lots of antibiotics and two weeks of hospitalization, he did not develop infection. Seven deep cuts required stitches.
Krishna was fine due to his usage of the pulse, but he was held in the ICU for a couple of hours to make sure he wasn’t suffering from internal bleeding or bruised bones, as he said he was extremely achy post-trauma.
Kitty, of course, had these nightmares for two reasons. She could now freely admit to both of these: She had gotten bacterial meningitis as a child, and she had gotten suicidal after her best-friend started treating her differently than before. This had resulted in two near-brushes with death. And there was the car crash too, where she had seen Yariulvus’s dead body on a stretcher. She did not want to be around any hospitals. She felt like she could feel the hospital in her sleep, some part of her was tethered to the walls around her. She dreamed of gashes and the caustic, seismic sound of a body slamming into a web of metal bars. Wings coming out of eye sockets and feet covered in blood. She had some internal realization that these were partly Winghead’s nightmares. In fact, one night, they woke up at the same time from a nightmare and ran into each other in the hallway on the way to the bathroom.
So when she got discharged, she didn’t visit Winghead. She went home and changed her clothes, from the light tan hospital garments to a pink baby tee and sweatpants. Instantly, she already felt more like herself. Ever since Harpy had gone away, the town had felt a little more like itself. No more scuttling things in the darkness or bodies floating in the water. She only had one heart, and that meant that she felt less, but she was feeling more…like things weren’t going to fall apart right in front of her. Or, things always felt like they were falling apart, but at least she could navigate it.
She brushed her hair, which was long enough to braid neatly down her back. She ordered Mcdonalds through DoorDash, just a Big Mac and fries. The driver was John Vaudan, which startled her. But it made sense that no one else was working except for the people who lived paycheck to paycheck. She tipped him with a five dollar bill.
She stood in the hallway outside her room, the floors so brown they were nearly black. The seams between the walls and the wood lining were freshly caulked. She checked the oily paper bag. She ate a fry. Her back hurt from lying down and sitting for so long. She went into her tiny room. Greta Gu Ma was still at work. Public defender case.
Her feet were cold, so she put on socks. Then she called Veel, who now always carried a Razor flip phone. She never used it unless Kitty called or texted. She picked up right away.
“Hello?”
“I’m home. I got a cab. Where are you?”
“I’m at the music store. I stepped out for a bit. Do you need something?”
Veel had started working again three days after the escape, helping Mrs. Choi fix her merchandise and throw away the debris caused by the whirlwind of Guests coming through her shops. Most of the expensive instruments survived because they were kept in the private sound proof room, and no Guests got inside. But outside, smashed ukeleles, acoustic guitars, cheap rental violins, violas, and music stands lay in a crumpled heap. Veel carried everything out with the help of Leo, Gemini, and Artemis, and then they swept the floors, vacuumed, beat out the dust, caulked, spackled, primed, painted, applied a light detergent to the upholstery, and scrubbed the counters and hardwood. They had to replace a handful of windows and one hanging light as well. Now Veel was tending the register again. There were practically no customers, aside from a gig band passing through whose lead guitarist needed new steel strings. Kitty suggested Veel learn the violin if she was bored.
“Can you come here? Or, I can go there. Whatever works. I - want to see you.” God, it was still so hard to admit that. She could barely choke it out, and cringed at her incompetency and chronic emotional constipation.
“Oh my god yeah get over here. I’m so-oo freaking bored.” Veel laughed, her voice crunchy through the terrible mic. Kitty could here a Bach concerto in the space between her loud laughs. She still had a thing for childish, guffaw-adjacent laughs. Veel and Winghead both laughed like “Ha! ha ha ha ha ha!” and it was great. She told Veel this.
“Charmed.” Veel’s grin was audible. “Get over here.”
Kitty knew she could walk, even with her fucked up atrophied legs, but she took the bus instead. It was impressive how fast public services returned back to normal. Buses, mail, police, fire department, city council, etc. Then again, they were somewhat more prepared to deal with the emergency after the FBI clued them in. Kitty felt strange now that she was no longer the go-to source for Harpy and Winghead-and-Veel-related news.
She got to Cordelia and took a left from the fountain, or, what was left of the fountain. Now it was just a gaping hole with caution tape around it and construction workers already going to work on it.
Choi’s Music was small and narrow at the front and opened up in the back. Kitty had been going there since she was fifteen to rent her clarinet. Veel was waiting at the counter, swiveling around in the high chair, visibly perking up when Kitty stood right in front of her.
Her face was amazing, as usual, but looking at the purplish bumpy edges around the pale brown scars was painful. Kitty could tell it hurt when she smiled.
“Kiss me?” she said. Kitty hummed and leaned in, giving her a little kiss on the corner of her mouth. She could feel the ridge of her chin scar under her fingertips where she cupped her face.
“Oh. Sorry - lip gloss.” She pointed at the corner of her own mouth as soon as they parted and Veel wiped her lips.
Veel hopped down from the chair and ducked under the counter door, coming out on Kitty’s side.
“I’m gonna ask Mrs. Choi if we can close up early - no one came in anyways.” Veel told her, and Kitty followed her up the stairs to Mrs. Choi’s apartment, where she was probably napping or sorting out finances.
Kitty inhaled deeply and exhaled. She accepted the cup of Oolong tea when Mrs. Choi offered it.
-
Winghead got out a week later, and this time, Kitty, Veel, Inez, and Sunny were waiting for him. Inez had flowers and a balloon in the shape of a heart. Sunny had brought him his clothes. Kitty didn’t bring anything, so she offered to buy Winghead tea when he was rolled out on a wheelchair by the attendant. He shrugged and said sure. He changed in the back of the car, into the Adidas hoodie and jeans Sunny brought. Then they all got in and drove to the nearest tea house. Wing fell asleep almost immediately against Inez’s shoulder, giant bouquet of pink tulips in his lap. The flower-perfume smell was really strong, so Sunny rolled down a window.
They got tea, and then they also went to Wingstop.
“How’s Ani?” Winghead asked when he seemed fully awake. Sunny pursed his lips.
“She’s OK.” He said, evenly. “Studying for the AP tests.”
They had all taken those already, but Kitty supposed Anneke’s memory was too scrambled or missing for her to remember what she had learned.
No one said anything for a while. Winghead shivered slightly, a movement that even reached his wings, and Inez wrapped an arm around him.
--
A week later, and Veel found Kitty sitting blankly in the hall outside her room. On the hardwood floor. If she sat with her back perfectly pressed against the wall, and extended her feet, they reached the other side and she could snugly wedge herself within the width of the hall. The pressure felt nice, and it was always a little dim in the hallway because there was only one lightbulb.
Veel hesitated. “Hey.”
Kitty remained silent, unmoving, unseeing, slowly blinking. Veel couldn’t tell how long she’d been at this. Her eyes looked red-rimmed and dry.
Then, she croaked. “Hi.”
Veel sat next to her, not quiet hugging her knees to her chest but wrapping her arms loosely around herself.
“I’m good.” Kitty said before Veel could speak. Veel nodded slowly.
Kitty was tired. She could feel a faint buzzing in her head. She kind of wanted to die. She was wearing jeans and they felt weirdly loose around her ankles. Her feet were bare. She could feel the texture of the drywall underneath them. The pressure was both condemning and a lifeline.
“I don’t like my room.” Kitty said.
“It’s a bit small,” Veel nodded, picking up what she was putting down.
“I don’t feel like I live here.” Her stomach hurt. Painful press in her lower abdomen, probably from eating a heavy lunch and going straight to bed afterward. “I can’t relax at all. I feel like a houseguest, or - or like a couch crasher. I want to go home.” She explained. “But not home home. I don’t know. I don’t really feel right anywhere.”
Kitty knew she scared Veel sometimes with how she talked. During their worst fight, Veel screamed that she was afraid Kitty was going to disappear or die the moment she stopped willing herself to be alive. That really hurt Kitty, and that night, when Veel had forced Mon to return to the Silverlands with her, Kitty had tried to go to sleep forever, outside in the forest, lacking the strength or will to walk home. She hoped she could will herself to go missing. It was only Winghead’s good conscious that saved her that time. She couldn’t help feeling evil after that, like some terrible selfish person, especially not when Winghead was giving her that angry, hollow, concerned look as she tried to explain to Greta what she was doing.
“I have a flat affect.” She said. “The doctor in the psychiatric wing said so. It’s caused by depression.”
She could see Veel trying to understand, rolling the words around in her head. “A flat affect.”
“Yes. It means I don’t feel emotions as strongly. They’re being suppressed.”
“You are…talking a bit flatly.” Veel noted. Kitty nodded.
“I felt so much when I had yours and Wing’s hearts. I couldn’t stop feeling these powerful waves and waves of emotion. It was - fascinating, and kind of amazing, but it was obviously too much - and I broke. That’s when the spell broke. And then I was just left with my own feelings. My own heart. Which is already - it’s already ruined. I don’t know if I can fix it, or if a therapist can fix it. I might be like this forever.”
“You’ve always talked like this.” Veel said. “Ever since the spell broke, you’ve been like this. At least for as long as I’ve known you. Was it like this before you came to the U.S.A.?”
“It started when I was thirteen I think.” Kitty mumbled. “Well, I’m not sure, I think people started noticing my lack of reaction when I was about to leave. Fourteen, then, maybe.”
“My dad - he was like this. Even before my mom disappeared.” Veel said, surprising Kitty. Veel wasn’t touching her, but they were sitting so close that Kitty could feel a bit of warmth from where their shoulders were adjacent, and it tickled. She rubbed her own bicep aggressively, trying to slough the feeling off of herself. “You could tell there was something wrong with him. It was the stress, I think. He was the weakest in our family, and so people ragged on him about that his whole life. I couldn’t fix him. No one could…but no one tried, either. He was - exhausting. But I didn’t want him to die.”
“Exhausting. You said - you said that I was - exhausting, right?” It had been during their fight.
Veel grimaced. “I’m so sorry, Kitty. I was projecting, I think. You reminded me of him. Your symptoms lined up with his. I got scared. I didn’t want to see you destroy yourself.”
Kitty said nothing for a while. “You said not to apologize -”
“Baby.”
“I didn’t know - I …”
“Kitty, no, it’s my fault.”
Kitty waved a hand and shook her head. “I forced you into my mess - I made it your responsibility to care for me…I made you afraid for me - when you shouldn’t even have known I - existed.”
“You said sorry. I forgive you.” Veel said. “You’ve done so much for me, Kitty.”
Kitty sighed. “It’s never going to be enough.”
“You’re speaking in extremes.”
“I know I am. I know …”
She trailed off, getting silent again. She knew. Of course she did. She was the smartest person in her whole school, and she definitely didn’t pioneer the field of Biology by being unobservant. She knew every faucet of her sickness, intimately. She just…forgot sometimes.
They sat like that for 70 minutes, Veel lightly dozing off and on, and then they heard Greta Gu-Ma’s key in the door. Kitty gingerly bent her legs, and began to stand up. Slowly, moving wrongly. Face blank. Veel must have been worried, because she placed a hand on Kitty’s lower back and helped her straighten out. Kitty let herself be maneuvered.
“I need to sleep.” Kitty said, voice broken. Veel nodded. She took her to her bedroom and helped her get under the covers.
“You’re so-.” Kitty whispered, tracing Veel’s chin scar with her finger as Veel tucked her in. “It’s amazing. You’re so steady. I don’t deserve you.”
Veel kissed her forehead.
They slept in the same bed that night. Kitty put her arms around Veel’s waist like she was a giant teddy bear. Veel’s stomach was astoundingly flat and hard. The nape of her neck smelled like pears. Kitty thought about what they had talked about and she cried as softly as possible. Veel breathed heavily.
#my art#my ocs#oc art#kitty chau#kitty zhou#veel drake#you ate my heart#my writing#writeblr#oc story#wlw#oc lore#long post
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Acromegaly
Overview
Acromegaly is a rare hormonal disorder that results from excessive production of growth hormone (GH) by the pituitary gland. This condition usually develops slowly over several years and is often not diagnosed until later stages. In most cases, acromegaly is caused by a benign tumor in the pituitary gland, called pituitary adenoma, that produces too much GH. Rarely, acromegaly can also be caused by tumors in other parts of the body that produce GH-releasing hormone (GHRH) or by non-tumor-related causes. The excess GH in acromegaly leads to an overgrowth of bones and tissues in the body, especially in the hands, feet, face, and internal organs. This results in a range of symptoms that can include: - Enlarged hands and feet - Coarse facial features - Increased sweating - Fatigue - Headaches - Joint pain - Carpal tunnel syndrome - Sleep apnea - Vision problems - Hypertension - Diabetes mellitus Acromegaly can also increase the risk of certain health problems, such as heart disease, stroke, and colon polyps. Treatment options for acromegaly include surgery to remove the pituitary tumor, medications to reduce GH production or block its effects, and radiation therapy. Treatment can improve symptoms, prevent complications, and reduce the risk of long-term health problems. Regular monitoring and follow-up care are important for managing this condition.
Symptoms
The symptoms of acromegaly can vary widely from person to person and can develop slowly over several years. Some of the common signs and symptoms of acromegaly include: - Enlarged hands and feet: The bones in the hands and feet grow larger, and the fingers and toes become thicker and wider. - Coarse facial features: The bones in the face, especially the jaw and forehead, become more prominent, and the nose and lips may also increase in size. - Increased sweating: People with acromegaly often experience excessive sweating, particularly at night. - Fatigue: People with acromegaly may feel tired or lack energy, even after a good night's sleep. - Headaches: Chronic headaches are a common symptom of acromegaly, and they can be severe. - Joint pain: The growth of bones and tissues can cause joint pain and stiffness, particularly in the hips, knees, and shoulders. - Carpal tunnel syndrome: The growth of tissues in the wrist can compress the median nerve, causing carpal tunnel syndrome. - Sleep apnea: Enlargement of the soft tissues in the throat can cause sleep apnea, a condition in which breathing stops briefly during sleep. - Vision problems: The enlarged pituitary gland can press against the optic nerves, causing vision problems or even vision loss. - Hypertension: Excessive growth hormone can cause high blood pressure. - Diabetes mellitus: The excess growth hormone can also cause insulin resistance, leading to high blood sugar levels and an increased risk of diabetes mellitus. It's important to note that not all people with acromegaly experience all of these symptoms. Some people may have mild or no symptoms, while others may experience more severe symptoms. If you're experiencing any of these symptoms, it's important to see a doctor for an evaluation.
When to see a doctor
If you have any symptoms of acromegaly, it's important to see a doctor for an evaluation. Some of the common symptoms include enlarged hands and feet, coarse facial features, excessive sweating, fatigue, chronic headaches, joint pain, carpal tunnel syndrome, sleep apnea, vision problems, hypertension, and diabetes mellitus. In addition, if you have a family history of acromegaly or have a condition that increases your risk of developing this disorder, such as multiple endocrine neoplasia type 1 (MEN1) or Carney complex, you should talk to your doctor about screening for acromegaly. Early diagnosis and treatment of acromegaly can prevent or minimize the development of complications associated with this disorder, such as heart disease, stroke, and colon polyps. If you suspect that you or a loved one may have acromegaly, it's important to see a doctor as soon as possible. Your doctor can order blood tests to check for elevated levels of growth hormone and insulin-like growth factor-1 (IGF-1), which are markers of acromegaly. Imaging tests, such as magnetic resonance imaging (MRI), may also be ordered to visualize any pituitary tumors. Treatment options for acromegaly are available and can help manage the symptoms and reduce the risk of complications.
Causes
Acromegaly is caused by the overproduction of growth hormone (GH) by the pituitary gland, which is a small gland located at the base of the brain. The excess GH is usually caused by a benign tumor, called a pituitary adenoma, that grows on the pituitary gland and produces too much GH. In rare cases, acromegaly can also be caused by tumors in other parts of the body that produce GH-releasing hormone (GHRH), which stimulates the pituitary gland to produce GH. These tumors are usually found in the pancreas, lungs, or adrenal glands. Other less common causes of acromegaly include: - Familial acromegaly: In rare cases, acromegaly can be inherited in an autosomal dominant pattern, which means that a person only needs to inherit one copy of the abnormal gene from one parent to develop the disorder. - Non-tumor-related causes: In very rare cases, acromegaly can be caused by certain medical conditions, such as McCune-Albright syndrome, which is a rare genetic disorder that causes abnormal bone growth and hormonal imbalances. Acromegaly usually develops slowly over several years, and the symptoms may not be noticeable for a long time. Early diagnosis and treatment are important to prevent complications associated with this disorder. If you suspect that you may have acromegaly or have a family history of the disorder, it's important to talk to your doctor about screening and testing for this condition.
Risk factors
There are several risk factors associated with the development of acromegaly, including: - Age: Acromegaly can occur at any age, but it is more common in middle-aged adults. - Gender: Acromegaly affects both men and women equally. - Family history: People with a family history of acromegaly or multiple endocrine neoplasia type 1 (MEN1) or Carney complex have an increased risk of developing the disorder. - Medical history: People who have had radiation therapy to the head or neck or have a history of pituitary tumors are at an increased risk of developing acromegaly. - Genetics: Some genetic mutations have been associated with an increased risk of developing pituitary tumors, which can lead to acromegaly. - Insulin resistance: People with insulin resistance, which can occur in conditions such as obesity or type 2 diabetes, may be at an increased risk of developing acromegaly. It's important to note that having one or more of these risk factors does not necessarily mean that you will develop acromegaly. However, if you have one or more of these risk factors, it's important to be aware of the signs and symptoms of acromegaly and to talk to your doctor about screening and testing for the disorder. Early diagnosis and treatment are important to prevent complications associated with this disorder.
Complications
Acromegaly can lead to a number of complications if left untreated or poorly managed, including: - Cardiovascular disease: Excess growth hormone can cause the heart to work harder, leading to an increased risk of hypertension, heart disease, and stroke. - Diabetes: Acromegaly can lead to insulin resistance, which can increase the risk of developing type 2 diabetes. - Sleep apnea: Enlarged soft tissues in the mouth and throat can obstruct breathing during sleep, leading to sleep apnea and poor quality sleep. - Joint problems: Excess growth hormone can cause bones and cartilage to grow abnormally, leading to joint pain and arthritis. - Carpal tunnel syndrome: Enlarged bones and tissues in the hands can compress the median nerve, causing numbness, tingling, and weakness in the hands and wrists. - Vision problems: Enlarged pituitary tumors can compress the optic nerve, leading to vision problems and even blindness. - Colorectal polyps and cancer: People with acromegaly are at an increased risk of developing polyps in the colon, which can lead to colorectal cancer if left untreated. - Increased risk of infections: People with acromegaly are at an increased risk of developing infections due to the effects of excess growth hormone on the immune system. - Psychosocial problems: People with acromegaly may experience depression, anxiety, and social isolation due to the physical and emotional effects of the disorder. It's important for people with acromegaly to receive early and appropriate treatment to prevent or manage these complications. Treatment options for acromegaly may include surgery, radiation therapy, and medication, depending on the underlying cause and severity of the disorder. Read the full article
#Acromegaly#benigntumor#care#Causes#development#diagnosis#endocrinesystem#enlargedhandsandfeet#excesshormone#excessivesweating#features#full#GH#gigantism#growth#growthhormone#health#hormonaldisorder#long-term#men#mouth#pituitarygland#produce#risk#signs#sleep#symptoms#Treatment#women
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What is Cancer? A Comprehensive Overview
Cancer stands as one of the most challenging and complex health issues faced by society today. Even with remarkable advancements in medical research, it continues to affect millions of people worldwide. This article aims to provide a detailed look at cancer, covering its progression, different types, root causes, treatment methods, and ways to prevent it. By shedding light on the nature of cancer, we can improve our grasp of its intricacies and the steps needed to combat it.
Understanding Cancer
Malignancy (a general term for cancerous growths) isn’t just one disease; it’s a collection of related conditions characterized by the uncontrolled growth and division of abnormal cells in the body. Normally, cells follow a regular cycle of growth, division, and death. When this cycle is disrupted, it can lead to the formation of a mass of cells, which we commonly call a tumor. Tumors can be categorized as benign (non-cancerous) or malignant (cancerous). Malignant tumors can invade nearby tissues and spread to other parts of the body, known as metastasis.
The Cellular Basis of Cancer
The human body consists of trillions of cells, each containing DNA that serves as a guide for their functions. Cancer arises when mutations occur in this DNA, disrupting the normal processes of cell growth and division, leading to cancerous cell formation.
The key characteristics of malignant cells, often referred to as the “hallmarks of malignancy,” include:
Continuous proliferative signaling: Malignant cells divide uncontrollably.
Evasion of growth inhibitors: They bypass the mechanisms that usually limit cell growth.
Resistance to cell death: Malignant cells avoid programmed cell death, known as apoptosis.
Replicative immortality: They can divide endlessly.
Induction of angiogenesis: They stimulate the creation of new blood vessels to secure a nutrient supply.
Tissue invasion and metastasis: They can spread to other parts of the body.
Types of Cancer
There are over 100 unique types of malignancies, categorized based on the tissue or organ they originate from and the specific cell types involved.The main categories are:
Carcinomas: These cancers develop from epithelial cells that line various organs and tissues, with examples including breast, lung, colon, and prostate cancer.
Sarcomas: These cancers originate in connective tissues, such as bones, muscles, and fat.
Leukemias: This group includes blood cancers that start in the bone marrow, leading to the overproduction of abnormal white blood cells.
Lymphomas: These cancers affect the lymphatic system, which plays a crucial role in the immune system.
Cancers of the brain and spinal cord: Known as central nervous system cancers, this category includes gliomas and meningiomas.
Causes and Risk Factors Malignancies develop due to a complex mix of genetic, environmental, and lifestyle factors. The main causes and risk factors include:
Genetics: Inherited mutations, especially in the BRCA1 and BRCA2 genes, significantly increase the chances of cancers like breast and ovarian tumors.
Lifestyle Choices: Behaviors such as smoking, heavy drinking, poor diet, and lack of exercise can greatly raise the risk of cancer.
Environmental Factors: Exposure to carcinogens, such as ultraviolet (UV) rays, air pollution, and toxic substances like asbestos and benzene, can trigger the onset of malignancies.
Infections: Certain viruses and bacteria, including human papillomavirus (HPV), hepatitis B and C, and Helicobacter pylori, are associated with tumor development.
Age: The risk of developing cancers tends to rise as people get older, largely due to the buildup of genetic mutations and a weakening immune system.
How Malignancies are Diagnosed Early detection of cancerous conditions greatly improves the chances of successful treatment. Common diagnostic methods include:
Imaging Techniques: X-rays, CT scans, MRIs, and ultrasounds are used to see tumors.
Biopsy: Tissue samples are examined under a microscope to confirm the presence of cancer.
Blood Tests: Tumor markers, such as PSA (prostate-specific antigen) for prostate malignancy or CA-125 for ovarian malignancy, can indicate the possibility of malignancy.
Genetic Testing: Identifying mutations in genes like BRCA1 can help assess malignancy risk or confirm a diagnosis.
Treatment of Malignancies Treatment strategies are based on the type, stage, and location of the tumor, as well as the patient’s overall health. Common methods include:
1. Surgery: This technique involves removing the tumor along with surrounding tissues and is especially effective for tumors that are localized.
2. Radiation Therapy: This approach uses high-energy rays or particles to destroy abnormal cells and is often combined with other treatments.
3. Chemotherapy: This method employs drugs to target and kill rapidly dividing cells. While effective, it can cause side effects like nausea and fatigue.
4. Targeted Therapy: This strategy focuses on specific molecules that drive abnormal cell growth, minimizing damage to healthy cells.
5. Immunotherapy: This treatment harnesses the body’s immune system to fight cancer, with options like checkpoint inhibitors and CAR-T cell therapy.
6. Hormone Therapy: For hormone-dependent tumors, such as those in breast and prostate cancers, medications that block hormones are used.
7. Stem Cell Transplants: This procedure replaces damaged bone marrow in blood-related cancers, such as leukemia.
Challenges in Treating Oncological Diseases Managing tumors comes with several challenges:
Drug Resistance: Cancer cells can adapt, reducing the effectiveness of treatments.
Metastasis: Tumors that spread can complicate the treatment process significantly.
Side Effects: Many treatments can harm healthy cells, leading to unwanted side effects.
Cost: Advanced therapies, like immunotherapy, often carry substantial costs.
Advances in Research on Malignancies
Ongoing research is enhancing our understanding of tumors and their treatment options. Key advancements include:
Precision Medicine: Tailoring treatments to fit an individual’s genetic profile.
Liquid Biopsies: Using blood tests to detect tumors early on.
Artificial Intelligence (AI): Enhancing diagnostic accuracy and predicting treatment outcomes.
Cancer Vaccines: Developing preventive vaccines like HPV and investigating new therapeutic vaccines.
Preventing Tumors and Other Malignancies Not every neoplasm can be avoided, but adopting a healthy lifestyle and minimizing exposure to risk factors can greatly lower the likelihood of developing cancer. Key prevention strategies include:
Steering Clear of Tobacco: Smoking is a major cause of lung cancer and other types of tumors.
Eating a Nutritious Diet: A diet abundant in fruits, vegetables, and whole grains, while limiting processed foods and red meat, can reduce the risk of neoplasms.
Staying Active: Regular physical activity helps maintain a healthy weight and decreases the chances of tumor formation.
Protecting Your Skin: Using sunscreen and avoiding tanning beds can significantly reduce the risk of skin cancers.
Getting Vaccinated: Vaccines for HPV and hepatitis B can help prevent cancers linked to these viruses.
Regular Screenings: Consistent medical check-ups and screenings, such as mammograms, colonoscopies, and Pap smears, are crucial for the early detection of cancers.
Living with a Diagnosis of Malignancy A malignancy diagnosis can profoundly affect an individual’s life, bringing about numerous physical, emotional, and financial challenges. During this tough period, the backing of family, friends, healthcare providers, and support groups is crucial. Recent advancements in palliative care aim to improve the quality of life for those facing advanced malignancies, focusing on pain management and emotional well-being.
Conclusion Cancer is a multifaceted health concern that demands a comprehensive approach to prevention, diagnosis, and treatment. While significant progress has been made, ongoing research and teamwork are essential for improving patient outcomes and ultimately finding a cure. By deepening our understanding of these diseases and their effects on the body, we empower individuals to make informed health decisions and strive for a future with fewer cancer-related challenges.
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What is a Malignant Neoplasm? Causes & Symptoms
Cells are the basic structural and functional units of life. They grow, replicate, and then die automatically (the process called apoptosis).
Problems arise when cells do not die and grow abnormally. This abnormal growth of cells in tissues is known as a neoplasm, which can be classified into two types: noncancerous (benign) and cancerous (malignant).
Benign tumors grow very slowly and do not spread beyond their point of origin. In contrast, malignant neoplasms are cancerous tumors. This is an interesting topic to explore, so let’s delve into the details.
What is a Malignant Neoplasm?
A malignant neoplasm, also known as a cancerous tumor, is characterized by uncontrolled cell growth and division. This abnormal growth can develop in any part of the body, including the breast, skin, prostate, bladder, cervix, endometrium (lining of the uterus), lung, colon, rectum, liver, bones, brain, and more.
Having gained a basic understanding of malignant neoplasms, it is essential to learn about the causes and symptoms associated with them. This knowledge will help you connect the dots and achieve a clearer understanding of the disease.
Causes of Malignant Neoplasm
Researchers are still uncertain about the exact causes of tumors. Generally, cancerous tumors develop as a result of DNA mutations within cells. Your DNA contains genes that direct how cells operate, grow, and divide. When DNA changes, it can lead to cancer.
Below are a few factors that can cause your genes to mutate, resulting in benign or malignant tumor growth:
Genetics
Immune disorders
Viruses
Overexposure to radiation
Chemical toxins
Age
Hormones
Smoking
Alcohol consumption
Obesity
Symptoms of Malignant Neoplasm
Symptoms of malignant neoplasms vary based on the affected area of the body. For instance, individuals with brain tumors may experience headaches, seizures, balance problems, and more. In contrast, those with colon cancer may suffer from abdominal pain or changes in stool.
Here are some general signs and symptoms associated with, but not specific to, cancer:
Fatigue
Lumps
Weight changes, including unintended loss or gain
Changes in the skin, such as yellowing, darkening, or redness; sores that do not heal
Changes to moles
Changes in bowel or bladder habits
Persistent cough or difficulty breathing
Difficulty swallowing
Persistent indigestion or discomfort after eating
Unexplained muscle or joint pain
Unexplained fevers or night sweats
Unexplained bleeding or bruising
While the above are visible symptoms, some patients may not experience any symptoms at all, or they may not realize their condition until it reaches an advanced stage.
For students preparing for an MD in Medicine, basic information is insufficient; they need to be aware of every aspect of the topic. To gain a deep understanding of malignant neoplasms, including reasons for asymptomatic cases and the diagnostic methods used to detect abnormal cell growth, enrolling in an MD course in Medicine is crucial.
Details About the Course
Understanding a complex subject is not easy, and to achieve a comprehensive knowledge of malignant neoplasms, one needs to learn it in an engaging and accessible way. That’s why this course is considered one of the most reliable resources for students.
The course includes detailed MD Medicine video lectures that cover procedures, enabling students to understand practical skills through a case-based approach. Are you eager to discover what more the course has to offer? Visit DigiNerve now!
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Early Signs of Cancer in Dogs You Should Watch Out For
Hearing the word "cancer" is a pet parent's worst nightmare, and the thought of a beloved dog battling this disease can be heartbreaking. Unfortunately, cancer is one of the leading causes of death among dogs. However, by being aware of the early signs and understanding potential risks, pet owners can take proactive steps to ensure their dog's health and well-being.
In this blog, we’ll cover the early signs of cancer in dogs, the most common types, and the importance of early detection and treatment.
How Common Is Cancer in Dogs?
Cancer is more common in dogs than many people realize. Studies estimate that approximately 1 in 4 dogs will develop cancer at some point in their lives, with the risk increasing as they age. Some breeds, especially large breeds such as Golden Retrievers, Rottweilers, and Boxers, are more prone to certain types of cancer. Though the thought of cancer can be distressing, recognizing early warning signs can make a significant difference in treatment success.
Early Signs of Cancer in Dogs
Identifying cancer in its early stages can be challenging since many symptoms mimic other health conditions. However, there are several key signs that pet owners should be aware of:
Unexplained lumps or bumps
Swelling that doesn’t go away
Sudden weight loss or gain
Loss of appetite
Difficulty eating or swallowing
Lethargy or general weakness
Persistent coughing or difficulty breathing
Lameness or difficulty walking
Unusual discharges (from the nose, mouth, or other areas)
Non-healing wounds
These symptoms do not always indicate cancer, but if you notice any of these signs in your dog, it’s essential to consult a veterinarian for further evaluation.
Common Types of Cancer in Dogs
Just like humans, dogs can develop cancer in various parts of their body. Some of the most common types of cancer in dogs include:
Lymphoma: Affects the lymphatic system and is marked by swollen lymph nodes, weight loss, and lethargy.
Mast Cell Tumors: These skin tumors can range from benign to aggressive, often appearing as lumps that change in size.
Osteosarcoma: A type of bone cancer common in large breeds, causing pain, swelling, and lameness.
Hemangiosarcoma: A cancer of the blood vessels, often found in the spleen or heart, which may cause sudden internal bleeding.
Mammary Gland Tumors: These tumors, common in unspayed female dogs, affect the mammary glands and can be either benign or malignant.
Early Detection and Diagnosis
Early detection is critical for improving treatment outcomes. If you notice any of the above signs, it's important to take your dog to the vet for a thorough examination. Diagnostic tools like fine-needle aspiration, biopsies, bloodwork, and imaging (X-rays, ultrasound) help confirm the presence of cancer and guide treatment plans.
Conclusion
While the thought of cancer in dogs is distressing, early detection and treatment can make a significant difference. By staying vigilant and monitoring your dog for unusual symptoms, you can catch potential problems early and seek timely medical advice. Regular veterinary checkups, a balanced diet, and maintaining your dog’s overall health are the best ways to support their well-being and longevity.
#cat#pet care#pet clinic#pets#pet health#delhincr#veterinary doctor#dog#gurgaon#veterinary doctor in gurgaon#cancer#cancer treatment#cancer in dogs
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Understanding Pituitary Tumors: Treatment Options Explained
Pituitary tumors, although often benign, can have significant implications for health due to their location at the base of the brain. These tumors can disrupt the normal functioning of the pituitary gland, which is crucial for hormone regulation. The treatment of pituitary tumors requires a comprehensive understanding of the various types of tumors, their symptoms, potential complications, and the most effective surgical and non-surgical treatment options available. This article delves into the complexities of pituitary tumors Treatment detailing the treatment options and highlighting the expertise of specialists like Newport Beach and Orange County.
What Are Pituitary Tumors?
Pituitary tumors are abnormal growths that develop in the pituitary gland, a small gland located at the base of the brain. The pituitary gland is often referred to as the “master gland” because it produces hormones that regulate various bodily functions, including growth, metabolism, and reproductive processes. While most pituitary tumors are non-cancerous (benign), they can still lead to significant health issues due to their effect on hormone production and their proximity to critical structures within the brain.
Common Types of Pituitary Tumors
Pituitary Adenomas: These are the most common type of pituitary tumors, accounting for 15-20% of primary brain tumors. They can be classified into functional adenomas, which produce excess hormones, and non-functional adenomas, which do not secrete hormones.
Acromegaly: This condition is caused by a growth hormone-secreting adenoma. Excess growth hormone leads to abnormal growth of bones and tissues, resulting in characteristic features such as enlarged hands, feet, and facial features.
Cushing’s Disease: Caused by an ACTH-secreting adenoma, Cushing’s disease results in elevated cortisol levels, leading to a range of symptoms, including weight gain, high blood pressure, and mood changes.
Prolactinoma: This type of adenoma leads to excess production of prolactin, which can cause infertility, irregular menstrual cycles, and breast discharge in women, and sexual dysfunction in men.
Craniopharyngioma: Although not a true pituitary tumor, craniopharyngiomas arise near the pituitary gland and can cause hormonal imbalances and vision problems.
Rathke’s Cleft Cyst: These are benign cysts that can develop in the pituitary gland and may cause symptoms if they grow large enough to compress surrounding structures.
Hypopituitarism: This condition, characterized by the underproduction of one or more of the pituitary hormones, can result from various causes, including the presence of a tumor.
Symptoms of Pituitary Tumors
The symptoms of pituitary tumors can vary widely, depending on the type of tumor and whether it is secreting hormones. Common symptoms include:
Headaches: Often the first symptom reported by patients, headaches can be persistent and may worsen over time.
Vision Problems: Tumors can press on the optic nerves, leading to vision loss or double vision.
Hormonal Imbalances: Symptoms related to hormonal dysregulation, such as changes in menstrual cycles, infertility, weight changes, and changes in libido, can occur depending on the type of tumor.
Fatigue and Weakness: Patients may experience general fatigue or weakness due to hormonal imbalances.
Mood Changes: Depression, anxiety, and other mood disturbances can arise as a result of hormonal fluctuations.
Diagnosis of Pituitary Tumors
Diagnosis typically begins with a thorough medical history and physical examination. If a pituitary tumor is suspected, the following tests may be conducted:
Magnetic Resonance Imaging (MRI): This imaging technique provides detailed images of the brain and pituitary gland, helping to identify the size and location of the tumor.
Hormonal Blood Tests: Blood tests can measure hormone levels to determine if the pituitary gland is functioning properly.
Visual Field Testing: This test assesses any changes in vision that may indicate pressure on the optic nerves.
Pituitary Tumors Treatment Options
Once diagnosed, the treatment plan for pituitary tumors is tailored to the individual, considering the type of tumor, its size, the symptoms it causes, and the overall health of the patient. Treatment options include:
1. Observation
In cases where the tumor is small, non-functional, and not causing significant symptoms, a "watch and wait" approach may be recommended. Regular monitoring through MRI scans and hormonal assessments can ensure that any changes are caught early.
2. Medication
For functional tumors, particularly prolactinomas, medication is often the first line of treatment. Dopamine agonists, such as cabergoline and bromocriptine, can effectively reduce tumor size and hormone levels. These medications are particularly effective for prolactin-secreting adenomas and are associated with fewer side effects compared to surgery.
3. Surgery
Surgical intervention is often necessary for larger tumors or those causing significant symptoms. specializes in endoscopic transsphenoidal surgery, a minimally invasive technique that allows access to the pituitary gland through the nasal cavity. This approach offers several advantages:
Reduced Recovery Time: Patients typically experience faster recovery compared to traditional open surgery.
Less Pain and Scarring: Smaller incisions result in less postoperative pain and minimal scarring.
Lower Risk of Complications: This approach minimizes damage to surrounding tissues and structures, reducing the risk of complications.
4. Radiation Therapy
In some cases, radiation therapy may be recommended, either as a primary treatment or as an adjunct to surgery, particularly for tumors that cannot be completely resected. Options include conventional radiation therapy and more advanced techniques such as Gamma Knife radiosurgery, which targets the tumor with high precision while sparing surrounding healthy tissue.
Post-Treatment Care and Follow-Up
After treatment for pituitary tumors, ongoing monitoring is essential to assess hormone levels and detect any recurrence of the tumor. Patients may require regular follow-up with an endocrinologist to manage hormonal imbalances and ensure optimal health outcomes.
Lifestyle Adjustments
Patients are often encouraged to make lifestyle adjustments to support their recovery and overall health. This may include:
Balanced Diet: Proper nutrition can help manage symptoms and improve overall well-being.
Regular Exercise: Engaging in regular physical activity can enhance mood and energy levels.
Stress Management: Techniques such as meditation, yoga, or counseling can help manage stress and emotional health.
Conclusion: The Importance of Specialized Care in Pituitary Tumors Treatment
The management of pituitary tumors requires a multidisciplinary approach, with expertise from neurosurgeons, endocrinologists, and other healthcare professionals. Dr. Robert Louis, a fellowship-trained neurosurgeon, offers cutting-edge treatment options for patients in Newport Beach and Orange County, specializing in minimally invasive techniques to ensure the best outcomes.By understanding the various types of pituitary tumors and their treatment options, patients can make informed decisions about their care. Whether through observation, medication, surgery, or radiation therapy, the goal is to alleviate symptoms, restore hormonal balance, and improve the quality of life.For anyone facing the challenges of pituitary tumors, seeking the guidance of a specialized treatment center can make all the difference. With the right approach and support, patients can navigate their journey toward recovery with confidence and hope.
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Cushing’s Disease & Pituitary Health: Understanding the Connection
Cushing’s disease is a rare but serious endocrine disorder caused by the overproduction of cortisol, often due to a tumor in the pituitary gland.
This excess cortisol can lead to a variety of symptoms that impact multiple systems in the body, and without proper treatment, it can have lasting effects on overall health.
At Endocrinology Associates, we understand the critical role the pituitary gland plays in regulating hormone levels and the complexities surrounding conditions like Cushing’s disease.
Our team is dedicated to diagnosing and managing this condition to help patients maintain optimal health.
What Is Cushing’s Disease?
Cushing’s disease occurs when a benign tumor (adenoma) on the pituitary gland produces excess adrenocorticotropic hormone (ACTH).
This hormone stimulates the adrenal glands to produce cortisol, leading to elevated levels in the bloodstream. Cortisol is vital for regulating stress responses, metabolism, and immune system function, but too much can have detrimental effects.
Symptoms of Cushing’s Disease
Cushing’s disease symptoms often develop gradually and may be mistaken for other health conditions, making early diagnosis critical. Common signs include:
Weight Gain: Particularly in the face (moon face), upper back, and abdomen, while arms and legs may remain thin.
Thinning Skin: Easy bruising and slow healing of cuts, scrapes, and insect bites.
Muscle Weakness: Loss of strength, especially in the upper arms and thighs.
High Blood Pressure: Cortisol's effect on salt and water balance can raise blood pressure.
Osteoporosis: Fragile bones that break more easily.
Mood Changes: Depression, anxiety, and irritability are common psychological effects.
Causes and Risk Factors of Cushing’s Disease
While the cause of most pituitary tumors remains unknown, there are several risk factors that can contribute to the development of Cushing’s disease:
Pituitary Adenomas: The primary cause, these noncancerous tumors lead to excessive ACTH production.
Prolonged Corticosteroid Use: Some cases are linked to long-term use of corticosteroid medications, which can mimic the effects of Cushing’s disease.
Treatment Options for Cushing’s Disease
At Endocrinology Associates, we provide individualized treatment options based on each patient's condition and the severity of their symptoms. Our goal is to restore hormonal balance and improve quality of life.
Surgery: Removing the pituitary tumor is the most common and effective treatment. Dr. Elena A. Christofides and her team work closely with neurosurgeons to ensure optimal outcomes for our patients.
Medications: If surgery isn’t an option or isn’t fully effective, medications can help control cortisol production or block its effects on the body.
Radiation Therapy: In cases where surgery and medication are not sufficient, targeted radiation therapy may be used to shrink the tumor.
Lifestyle Modifications: Managing diet, stress levels, and blood pressure can help mitigate symptoms while undergoing treatment.
Why Pituitary Health Matters
The pituitary gland, often called the "master gland," is responsible for regulating many of the body’s key functions by controlling hormone production.
Any disruption in its function, such as a tumor causing Cushing’s disease, can lead to significant health issues. Early detection and treatment are essential to preventing long-term complications.
Managing Cushing’s Disease with Endocrinology Associates
Dr. Elena A. Christofides and her expert team at Endocrinology Associates are dedicated to providing compassionate, patient-centered care. We work to diagnose Cushing’s disease early and develop personalized treatment plans that address both immediate symptoms and long-term health.
If you suspect you may be experiencing symptoms of Cushing’s disease, or if you have concerns about your pituitary health, schedule a consultation with Endocrinology Associates today.
Schedule a Consultation
Contact Endocrinology Associates today to learn more about how we can help you manage Cushing’s disease and support your pituitary health.
Location: 72 W 3rd Ave, 2nd Floor, Columbus, OH 43201 Phone: (614) 453-9999
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Types of Cancer that Develop in Children
Cancer in children is a rare but serious health risk. Pediatric cancers are primarily caused by genetic mutations or developmental processes, as opposed to adult malignancies, which are frequently influenced by environmental factors and lifestyle choices. Despite the hurdles, many juvenile malignancies are curable, particularly with early detection and sophisticated treatment. Understanding the many forms of malignancies that typically affect children can help parents and caregivers become more aware of the symptoms and intervene sooner. For families wanting the greatest level of care, selecting the best Pediatric hospital in Jaipur is vital in providing children with the specific attention they require during this critical period.
Common Types of Childhood Cancers
There are several types of cancer that commonly affect children. Each type presents unique challenges and requires specific treatments tailored to the child’s age, size, and overall health. Below is an overview of the most frequent childhood cancers:
1. Leukemia
Leukemia is the most common type of cancer in children, accounting for about 30% of all pediatric cancers. This cancer starts in the bone marrow, where blood cells are produced. The two main types of leukemia in children are:
Acute Lymphoblastic Leukemia (ALL): This is the most common form of leukemia in children. It occurs when the bone marrow produces too many immature white blood cells, which crowd out normal cells and lead to various symptoms like fatigue, fever, and bone pain.
Acute Myeloid Leukemia (AML): Though less common than ALL, AML is a more aggressive form of leukemia that affects both the bone marrow and blood, leading to infections, anemia, and easy bruising or bleeding.
Symptoms of leukemia often include fatigue, frequent infections, easy bruising, swollen lymph nodes, and unexplained weight loss. Early diagnosis and treatment, often including chemotherapy, can lead to successful outcomes.
2. Brain and Central Nervous System (CNS) Tumors
Brain tumors are the second most common type of childhood cancer. They can occur in various parts of the brain and spinal cord, and their symptoms depend on the tumor's location and size. The most common types of brain tumors in children include:
Medulloblastoma: This is the most common malignant brain tumor in children. It typically arises in the cerebellum, the part of the brain responsible for balance and coordination.
Gliomas: These tumors originate from glial cells in the brain and spinal cord. There are several subtypes, including astrocytomas and ependymomas, which can be benign or malignant.
Symptoms of brain tumors include headaches, nausea, vomiting, balance problems, seizures, and vision or hearing changes. Surgery, radiation therapy, and chemotherapy are commonly used treatments, and the prognosis depends on the tumor’s type and location.
3. Neuroblastoma
Neuroblastoma is a cancer that arises from immature nerve cells in young children, usually under the age of five. It typically starts in the adrenal glands on top of the kidneys, although it can also develop in the neck, chest, abdomen, or spine.
Neuroblastoma symptoms vary depending on where the tumor is located, but they may include abdominal pain, a lump in the abdomen or neck, weight loss, and difficulty breathing or swallowing. Neuroblastoma can be aggressive, although therapeutic options such as surgery, chemotherapy, radiation, and stem cell transplants have led to higher survival rates.
4. Wilms’ Tumor
Wilms’ tumor, or nephroblastoma, is a cancer of the kidneys that primarily affects children aged 3 to 4. It accounts for about 5% of all pediatric cancers. Wilms’ tumor usually manifests as a painless swelling or lump in the abdomen, sometimes accompanied by fever, nausea, or blood in the urine.
Most children with Wilms' tumor respond well to treatment, which typically involves surgery to remove the tumor, followed by chemotherapy and sometimes radiation. The prognosis is often excellent, especially when diagnosed early.
5. Lymphomas
Lymphomas are cancers of the lymphatic system, which is part of the immune system. There are two main types of lymphoma in children:
Hodgkin’s Lymphoma: This type of lymphoma is characterized by the presence of Reed-Sternberg cells and is more common in adolescents. Symptoms include swollen lymph nodes, fever, night sweats, and weight loss.
Non-Hodgkin’s Lymphoma (NHL): NHL is more common in younger children and tends to grow more aggressively than Hodgkin's lymphoma. Symptoms often include abdominal pain, swelling, and difficulty breathing.
Both types of lymphoma are treated with chemotherapy, and the success rate is high, especially for early-stage Hodgkin's lymphoma.
6. Rhabdomyosarcoma
Rhabdomyosarcoma is a cancer that develops in the soft tissues, particularly in the muscles that control voluntary movements. It can occur anywhere in the body but is most commonly found in the head, neck, bladder, and arms or legs. Symptoms vary depending on the location but may include pain, swelling, and the presence of a lump.
This cancer is typically treated with surgery, chemotherapy, and radiation therapy, and the prognosis depends on the tumor’s location and the extent of its spread.
7. Retinoblastoma
Retinoblastoma is a rare cancer of the retina, the light-sensitive tissue at the back of the eye. It primarily affects children under the age of 5. The most common sign of retinoblastoma is a visible whiteness in the pupil when light is shone into the eye, often noticed in photographs.
Treatment for retinoblastoma may include laser therapy, cryotherapy, chemotherapy, or, in severe cases, removal of the affected eye. Early diagnosis is key to preserving vision and preventing the spread of cancer.
8. Bone Cancers
Two main types of bone cancer affect children:
Osteosarcoma: The most common type of bone cancer in children, osteosarcoma usually develops in the long bones, such as the arms and legs, and is more prevalent in teenagers during growth spurts.
Ewing Sarcoma: This cancer can develop in both the bones and surrounding soft tissues and tends to affect adolescents and young adults.
Symptoms of bone cancer include bone pain, swelling, and fractures. Treatment usually involves surgery, chemotherapy, and sometimes radiation.
Conclusion
Childhood cancers, though rare, pose significant challenges for children and their families. Early detection and prompt, effective treatment can greatly improve the chances of survival and recovery. It’s important for parents to stay vigilant about unusual symptoms and seek medical care if they suspect something is wrong. For those navigating the complex world of pediatric cancer, selecting the best hospital in Jaipur for cancer treatment ensures that your child receives the best possible care, helping them on the road to recovery and giving them a brighter, healthier future.
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Where does cancer start?
Cancer begins when abnormal cells in the body grow uncontrollably, invading surrounding tissues. While normal cells follow a predictable life cycle of growth, division, and death, cancer cells bypass this process, continuing to grow and divide unchecked. This uncontrolled growth forms tumors, which can either be benign (non-cancerous) or malignant (cancerous). Malignant tumors invade nearby tissues and can spread to other parts of the body through a process called metastasis, leading to more severe health issues.
Where Does Cancer Start?
Cancer can start in almost any part of the body, as it originates from cells, which are the building blocks of all tissues and organs. The specific location where cancer begins is referred to as the primary site. There are over 100 types of cancer, categorized based on the organ or tissue of origin. For example, breast cancer begins in breast tissue, while lung cancer originates in the lungs.
The process that triggers cancer typically begins with genetic mutations in the DNA of cells. These mutations can be inherited, but more commonly, they result from environmental factors such as exposure to carcinogens, like tobacco smoke, radiation, and harmful chemicals. Other factors like diet, hormones, and chronic inflammation may also increase the risk of developing cancer. Even though not all cancers have a clear cause, understanding the triggers and pathways can be key in prevention and early detection.
Major Cancer Types and Where They Begin:
Carcinomas: These are the most common types of cancer and start in the epithelial cells that line the surface of organs and glands. Common examples include breast, lung, colon, and skin cancers.
Sarcomas: These cancers begin in connective tissues such as bones, muscles, and fat. Sarcomas are rarer but can be aggressive if not treated early.
Leukemias: This type of cancer starts in the blood-forming tissues like the bone marrow, leading to the production of abnormal blood cells.
Lymphomas: Lymphomas originate in the lymphatic system, which is part of the body’s immune defense. They are divided into Hodgkin and non-Hodgkin lymphomas.
Brain and spinal cord cancers: These start in the central nervous system, affecting brain function and overall body control.
The Role of Cancer Organizations
Organizations like the National Coalition for Cancer Survivorship (NCCS) play a crucial role in educating the public about cancer and supporting patients and survivors. NCCS provides resources on how cancer starts, preventive measures, and guidelines for managing life after a cancer diagnosis.
Cancer organizations also raise awareness about early detection, promote screening programs, and fund research to understand where and how cancer starts. By providing support networks and advocacy, these organizations ensure that patients receive comprehensive care from diagnosis through treatment and beyond, emphasizing the importance of survivorship care planning.
Understanding where cancer starts is fundamental for early detection and effective treatment, and organizations like NCCS continue to lead the fight against this complex disease.
To know more visit: https://canceradvocacy.org/
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Seeious post on the horny blog time, dont read if you're just here for the horny. It's a full vent post so. Be warned
Mental illness sucks :(
Just kinda feeling like I need someone to talk to but no one is around really. Its unusual for me, as I typically prefer to be left alone, but occasionally some part of my brain just yearns for socialization with anyone really. And I feel just generally kinda sad and lonely even though I know there's people who care about me. I dont have people reach out to talk to me often, if ever, and I end up reaching out to people to try and talk but I just feel awkward usually. I sometimes have to stop and wonder if people dont like me, or if im doing something wrong. Idk. Im just tired. Life's been hard lately, and im just drained.
I gotta vent somewhere and this is the closest thing I have to a void to shout into. I work a job for 15 an hour, and get weekly pay. But. Both my parents have been needing surgery after surgery because quite simply theyre both in their 70's (im adopted) and they didn't get that generational wealth like the stereotypical boomers did. We live paycheck to paycheck and for a while now ive been covering part of our bills while mom recovers from.. god, too much. She got breast cancer, then her knees had to be replaced because she has brittle bones and the cartilage literally wore out in both, then she got cateracts from the cancer drug she was taking to keep it from coming back, so we had to get surgery to remove those. And of course we had to deal wirh complications. She ended up with 5 fucking tears in her retina. So that was another surgery. So my original plan was to support the family qith half my income for like. 6 months and it's been almost a year.
Then dad. He has so many medical problems too but he makes the most money out of the three of us and he works at a fucking corporate grocery store. He's so broken down. He needs a knee replacement surgery, spinal repair, ankle and shoulder. He had a cancer scare too but they were all benign. All 14 fucking tumors were benign. So im hedging my bets that ill have to help with bills for another like fucking year at this rate. I only get 450 a week, which is a lot to some, but not when I'm also having to help with groceries gas and all this other bullshit. Im so scared that something will happen and we wont be able to scrape by. Its exhausting.
Im not giving up though. Too damn stubborn at this point. I'm not able to move out and live on my own even if I want to. Dont have the income. So I guess I just gotta ride it out.
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Imaging Techniques in Musculoskeletal Radiology: A Guide to Common Conditions and Effective Strategies
Musculoskeletal radiology is a specialized branch of medical imaging focused on diagnosing and managing disorders related to bones, joints, and soft tissues. It plays a crucial role in identifying various conditions, from fractures to complex diseases like arthritis. Understanding the common conditions in this field and the imaging strategies used can help practitioners and patients navigate treatment options more effectively.
Common Conditions in Musculoskeletal Radiology
Musculoskeletal radiology encompasses a wide range of conditions, many of which are common across different patient populations. One of the most frequently encountered issues is fractures. Whether due to trauma, stress, or underlying bone conditions, fractures require precise imaging to determine the extent of injury and plan appropriate treatment. Radiographs, or X-rays, are typically the first imaging modality used, providing clear visualization of bone structures.
Another common condition is osteoarthritis, a degenerative joint disease that affects millions of people worldwide. This condition is characterized by cartilage breakdown and bone structure changes, leading to pain and reduced mobility. Imaging is vital in diagnosing osteoarthritis, with X-rays being the most commonly used method. X-rays can show joint space narrowing, subchondral sclerosis, and osteophyte formation, which are hallmark signs of the disease.
Advanced Imaging Techniques for Soft Tissue Disorders
While X-rays are invaluable for assessing bone-related conditions, they are often insufficient for diagnosing soft tissue disorders. Advanced imaging techniques like magnetic resonance imaging (MRI) and Ultrasound are commonly used in these cases. MRI is particularly effective in visualizing soft tissues, such as muscles, tendons, and ligaments. It provides detailed images that help in diagnosing conditions like rotator cuff tears, ligament injuries, and muscle strains.
Ultrasound is another powerful tool in musculoskeletal radiology, especially for real-time evaluation of soft tissue conditions. It is often used to assess tendon and muscle injuries, bursitis, and nerve entrapments. Ultrasound is also helpful in guiding therapeutic injections, making it a versatile imaging modality in clinical practice. The dynamic nature of Ultrasound allows for the assessment of structures in motion, which can be particularly useful in diagnosing conditions that are position-dependent.
Role of Imaging in Diagnosing Inflammatory Conditions
Inflammatory conditions, such as rheumatoid arthritis and ankylosing spondylitis, are other critical areas where musculoskeletal radiology plays a significant role. Early and accurate diagnosis is essential for managing these chronic conditions, and imaging is a cornerstone. MRI and Ultrasound are often used to detect early signs of inflammation in joints and surrounding tissues. MRI is particularly useful for identifying synovitis, bone marrow edema, and erosions indicative of rheumatoid arthritis.
Ultrasound can also be used to detect inflammation, especially in peripheral joints. It is highly sensitive in identifying synovial thickening and increased blood flow, which are early markers of inflammatory arthritis. The ability to assess these conditions early in their course allows for timely intervention, which can prevent joint damage and improve long-term outcomes for patients.
Imaging Strategies for Tumors and Infections
Musculoskeletal radiology is also crucial in detecting and evaluating tumors and infections. Whether benign or malignant, bone tumors require detailed imaging for accurate diagnosis and staging. X-rays are often the first step, revealing abnormalities in bone structure that may suggest a tumor. However, advanced imaging techniques like MRI and Computed Tomography (CT) are necessary for further evaluation. MRI is particularly useful for assessing the extent of tumor invasion into surrounding soft tissues, while CT provides detailed images of bone architecture.
Infections of the musculoskeletal system, such as osteomyelitis, also require precise imaging for diagnosis and management. X-rays may show early signs of bone infection, but MRI is the preferred method due to its ability to detect early bone marrow changes. MRI can reveal the extent of the disease and help guide treatment decisions, such as the need for surgical intervention. In cases where an abscess is suspected, Ultrasound can guide aspiration and drainage, providing diagnostic and therapeutic benefits.
The Future of Musculoskeletal Imaging
Musculoskeletal radiology is continually evolving, with new imaging techniques and technologies that promise to enhance diagnostic accuracy and patient care. One such advancement is Dual-Energy CT (DECT), which can differentiate between various tissue types based on their chemical composition. This technology is particularly useful in assessing gout, as it can detect urate crystals in joints and soft tissues without requiring invasive procedures.
Artificial intelligence (AI) is also making its way into musculoskeletal imaging, offering the potential to improve the efficiency and accuracy of image interpretation. AI algorithms can assist radiologists in identifying patterns and anomalies that may be missed by the human eye, leading to earlier diagnosis and better treatment outcomes. As these technologies continue to develop, they promise to transform musculoskeletal radiology, making it even more effective in diagnosing and managing a wide range of conditions.
Musculoskeletal radiology is a dynamic and essential field in diagnosing and managing various conditions affecting bones, joints, and soft tissues. From fractures and degenerative diseases to tumors and infections, imaging techniques like X-rays, MRI, and Ultrasound are invaluable tools that guide clinical decision-making and patient care. As technology continues to advance, the future of musculoskeletal radiology looks promising, with innovations that will enhance the ability to diagnose conditions more accurately and treat them more effectively.
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Dr. Purvi Kadakia Kutty: Leading Pediatric Hematology & Oncology Specialist in Navi Mumbai
Pediatric Hematology and Oncology is a specialized branch of medicine dedicated to diagnosing and treating children with blood disorders and cancers. pediatric hematology & oncology in navi mumbai Dr. Purvi Kadakia Kutty stands out as a leading expert in this field, offering comprehensive care for children facing these challenging conditions. Her approach not only focuses on treatment but also emphasizes the importance of cancer prevention and early detection, ensuring the best possible outcomes for her young patients.
Understanding Pediatric Cancers
pediatric hematology oncology are a distinct group of cancers that occur in children and adolescents. Unlike adult cancers, which are often linked to lifestyle factors, pediatric cancers are usually the result of random genetic mutations. The most common types include leukemia, brain and spinal cord tumors, neuroblastoma, Wilms tumor, and lymphoma. Early detection and timely intervention are crucial in managing these cancers effectively, and this is where Dr. Purvi Kadakia Kutty’s expertise plays a vital role.
Dr. Purvi Kadakia Kutty, M.D. Pediatrics, FNB Pediatric Hematology & Oncology is a Consultant Pediatric Hematology & Oncology at Apollo Hospitals, Navi Mumbai.She is an Honorary-visiting consultant in the Division of Pediatric Hematology Oncology at L.T.M.G.H., Sion Hospital. She has experience of over 10 years in the field of Pediatric Hematology, Immunology & Oncology. She is also experienced in Pediatric Bone marrow transplantsfor benign and malignant hematological conditions.Kharghar, Navi Mumbai
The Role of Pediatric Hematologists and Oncologists
Pediatric hematologists and Child Oncologist like Dr. Purvi Kadakia Kutty are specialists trained to understand the unique needs of children with cancer. They not only provide treatment but also support families through the emotional and psychological challenges that come with a cancer diagnosis. These specialists are skilled in using advanced therapies tailored to the developmental stages of their young patients, ensuring treatments are as effective and minimally invasive as possible.
Prevention and Early Detection
While pediatric cancers are often not preventable, certain steps can be taken to reduce the risk and ensure early detection. Regular check-ups and being aware of the signs and symptoms of pediatric cancers are key. Some warning signs to watch for include unexplained weight loss, persistent pain in bones or joints, swelling or lumps, sudden vision changes, and easy bruising or bleeding.
Dr. Purvi Kadakia Kutty emphasizes the importance of awareness and education for parents and caregivers. By understanding the risk factors and symptoms, families can seek medical attention promptly, which can lead to early diagnosis and better treatment outcomes. Genetic counseling is also an important tool for families with a history of certain cancers, allowing them to understand their risks and take appropriate precautions.
At her practice in Kharghar, Navi Mumbai, Dr. Purvi Kadakia Kutty offers a comprehensive approach to pediatric hematology and oncology. Her care extends beyond just treating the disease; it includes supporting the overall well-being of the child and their family. This holistic approach includes nutritional guidance, psychological support, and long-term follow-up care to monitor the child's health post-treatment.
Dr. Kadakia Kutty is also involved in the latest research and treatment protocols, ensuring her patients have access to cutting-edge therapies. From targeted therapies and immunotherapy to stem cell transplants, her practice incorporates the most advanced treatments available, tailored to the specific needs of each child.
A cancer diagnosis in a child affects the entire family. Dr. Purvi Kadakia Kutty understands this and provides resources and support for families throughout their journey. This includes counseling services, support groups, and guidance on managing the day-to-day challenges of caring for a child with cancer. She believes in empowering parents with knowledge and support, enabling them to make informed decisions about their child's care.
The Future of Pediatric Cancer Care
The field of pediatric hematology & oncology in navi mumbai is continually evolving, with new treatments and strategies emerging regularly. Dr. Purvi Kadakia Kutty is at the forefront of these advancements, committed to improving survival rates and quality of life for her patients. Her dedication to research, prevention, and comprehensive care makes her a trusted name in pediatric cancer care in Navi Mumbai.
In conclusion, pediatric cancer care requires a specialized, compassionate approach that addresses the unique needs of children and their families. Dr. Purvi Kadakia Kutty's practice in Navi Mumbai exemplifies this, providing hope and healing to young patients battling cancer. Through prevention, early detection, and cutting-edge treatment, she is helping to shape a brighter future for children with cancer.
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Google Directions: Kharghar, Navi Mumbai.
Contact: +91 77381 62020
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