#lipoma causes

[dratefahmed1]

Short medical and Surgical Notes/ lipoma/Medical Lecture/Medical Video/Medical Students/no1doctor

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[seonghwasblr-moved]

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[l3irdl3rain]

Okay. Joey vet update. It’s long so I’ll put it under a cut.

They agree that the lump appears to be a lipoma (benign fatty tumor). And they agree that removing it would be best to keep it from getting any bigger. They’ll send it out for pathology to make sure it’s nothing to worry about.

They also mentioned that he seems to have fat deposits on the cheeks. Meanwhile his body has little to no body fat at all. They suspect his pectoral muscles are atrophied, leading to his fat depositing in weird places like his face. So all these years I thought Joey was a skinny boy he may have not been as skinny as I thought.

He just had bloodwork done and it looked good so they’re not worried about that. They did want to do some presurgical radiographs though. Those all looked pretty good, except they noticed what they believe to be aspergillosis. Aspergillosis is a respiratory disease caused by fungal spores. It is very possible he has had this for many years. He has never shown any symptoms and it might be many more years before he becomes symptomatic. But obviously it’s best to take care of it now.

He’s going to get some meds for the next few weeks and then have recheck radiographs on October 1st. If those look improved we’ll go ahead and schedule his surgery

[soft--dogs]

i'm back from the vet, the good news is the vet thinks boomer's tummy bump is just a benign lipoma. buuuuuut she's worried about where it's located, and how fast it's growing. since it's right above his peanus, if it gets any bigger it could impact how he pees and cause problems :/ she's also worried about that cluster of bumps on his hip, where that big floof patch is. she wants to remove it and send to be tested for cancer cells. they already tested it at the vet clinic and said it seemed like just fat cells (like a lipoma), but she's still concerned about it. she said i can wait and monitor both spots for growth, but that i should probably consider getting them removed soon :s

[shingekinomyfeelings]

Taurus is not doing great today. Obviously hurting a lot, and not as enthusiastic about food as he's always been. I've been pretty worried, but we're at the vet right now and literally just as I started to make this post, the vet came in to show us his x ray results. It looks like his spleen is being pressed out of place by something, which would definitely explain the pain. The blood test results should be in tomorrow and let us know if he needs an emergency splenectomy - if they're normal, we're probably looking at something like an internal lipoma causing compression, which would be a lot less scary. So, it really depends on what we see in the next 24 hours. I'm trying not to anticipate the worst. Keep your fingers crossed for him, please.

[leo-fie]

Over on a german language leftist subreddit I just had some guy tell me that fat people whose thighs are touching to the point where it causes health problems are so super rare that we shouldn't consider them in our politics, specifically with regard to cis-hetero society's insistence on pants.

They of course also said that it's not hard to loose enough weight to where your thighs aren't touching anymore and completely disregarded my argument that it's still oppressive to want fat people to conform to their standards, just because they think it's easy to be thin.

As if lipomas on the inner thighs aren't such a widespread thing that we literally have a word for it: Reiterhosen.

Anyway, I'm tired.

[setnet]

fun medical times general don't look warning if such things gross you out/you get angry about misdiagnosis etc

when I was a kid I was diagnosed with rheumatoid arthritis. Great, fine, explained why my knees (and hips though that wasn't picked up for another couple years) didn't bend past right angles and were approximately the shape of a pufferfish. With a bit of treatment I got most of the range of motion back and the puffiness reduced a bit.

there were a few things that never quite gelled like how my blood tests never showed inflammation, x-rays showed no damage in the joints, and anti rheumatic drugs were markedly less useful than simple pain medication and anti inflammatories. But those my GP could manage so the rheumatologists shuffled me off their books.

last year my GP said, well, it's been a decade since you saw a specialist and your pain seems to be getting worse but I don't want you on some of these pain meds forever so let's get someone to look at you. public system said no, there's no inflammation in the blood tests, she's not high priority. GP said, hm, still not happy, want to try private? Me with health insurance and in chronic pain etc said, sure, why not.

specialist says, well, I'm not sure there's much I can do, but let's get you an MRI of one of your knees so we can check what's going on in there.

ever had a medical appointment start with the words, 'your scan results were very interesting'?

turns out I do not have and have have had rheumatoid arthritis.

turns out I have something so rare that I couldn't find a single layperson language resource about it

he got a scan of the other knee and fished out one done of my hips age about fourteen and turns out not only do I have this extremely rare condition; where most people who get it only ever get it in one joint, I have it in four joints: both knees and both hips

this thing is called lipoma arborescens and it's basically just gunk. It limits range of motion and caused pain through purely mechanical obstruction. It can basically only be diagnosed through MRI imaging or cutting open the joint to look, and even MRI has become much better over time: looking at the fuzzy, low-res 15-year-old MRI of my hips, even through my thwarted fury about e misdiagnosis I can kind of see why they didn't catch it.

other key things about lipoma arborescens that distinguish it from rheumatoid arthritis: it doesn't damage bone; it doesn't cause inflammation; and it doesn't respond to anti rheumatic drugs.

recommended treatment is just to go into the joint and cut it out: 'early synovectomy'.

that caused me to choke on a laugh and tell the specialist, you're twenty years too late for early.

but it's one knee down now. Today a knee surgeon went in there and did his thing. In his exacting medical terminology he told me 'there was quite a bit of the stuff in there, but I got most of it out'.

So I'll have a bunch of physiotherapy to do and an exciting new scar across my knee cap. and if it helps, I guess we line up for rounds 2-4.

[sleepytoycollection]

ya sleepy friendo here is having a lipoma removed wednesday because it turns out it's been causing a good chunk of my shoulder pain. here's to hoping it helps and I'll be able to do more projects now

[mediend2]

Lipoma Causes, Symptoms, And Effective Prevention Methods

Lipoma is a common benign tumor that forms under the skin. It is composed of fat cells and can occur in any part of the body, but is most commonly found on the neck, shoulders, arms, and torso. Lipomas are non-cancerous and do not usually cause any harm, but they can be concerning due to their appearance and potential growth. There are different types of lipomas, such as superficial and deep-seated, which may vary in size and location. Lipomas are prevalent in the population, with about 1 in 100 people having them. Despite being harmless, addressing lipoma is important for overall health and wellness. In this article, we will provide a comprehensive understanding of lipoma, covering its causes, symptoms, diagnosis, treatment, and effective prevention methods.

Symptoms of Lipoma

· Lipoma typically presents as a soft, painless lump under the skin.

· It is commonly found on the neck, shoulders, back, arms, and thighs.

· The size of lipoma can range from small pea-sized to large grapefruit-sized.

· In rare cases, lipoma may cause pressure or discomfort if it grows near nerves or organs.

· Some people may experience multiple lipomas on their body.

It is important to note that lipoma symptoms may vary depending on the location and size of the lump. For example, a lipoma on the neck may cause difficulty in swallowing or breathing, while a lipoma on the thigh may cause discomfort when walking or sitting for long periods.

Read more

[hearth-and-veil]

I'm about to have to make one of the hardest decisions of my life and I don't know if I can do it.

I love my dog. She's the best dog in the world (as all dogs are). We just celebrated her 10th Gotcha Day and she was 2-3 years old when I got her. She's a Doberman, so she is well past her life expectancy.

She does have some quality of life. I think she's still happy. She still hops around like a puppy when we grab her leash to take her on a walk. But I know that quality of life is declining. She used to sleep in my bed almost every night. Now she can barely get up there, and she won't stay. She spends most of her day asleep. She's absolutely covered in lipomas, and more of them keep popping up. I can't even keep track anymore. She has some kind of hip issue that's causing nerve problems. She opened up a massive lick granuloma on her leg because of the nerve sensation, and it's been continually open for years. We can't get her to stop, even with medication, spinal manipulation, and laser therapy. She's having a harder time walking. The back yard is down a high set of stairs and she slips on them almost every day.

She was just diagnosed with laryngeal paralysis and she's not a good candidate for tie-back surgery.

As much as I wish it weren't a factor, the cost of her vet bills has gotten out of hand. We've already spent about $4,000 (USD) on her medical treatments this year. It'll be over $5,000 by the end of the year. We can't afford that. We absolutely can't afford it.

I know I'm going to have to euthanize her. I don't know if I'm keeping her alive when I should have already let her go because I can't bear it. I don't know if I'm trying to euthanize her prematurely. She has good days and bad days. If it were me (and I have a severe degenerative disability, so one day it will be) I would want to pass peacefully while the good days still outnumbered the bad.

I don't know what to do and there isn't a single choice I can make that I won't hate myself for later.

[dissociacrip]

I know you probably were thinking of people who have POTS and orthostatic hypotension when you said compression stockings aren't a mobility aid but on rare occasions it can be, because there are people with lymphedema and lipedema bad enough that they can't walk well unless they're wearing compression stockings (I would know, I have lymphedema though mine isn't severe enough to count as a visible disability). It's not in like. A mad way but I'm just sad everyone in the disability community forgets lymphedema or lipedema exist and just assume it's a fat person disease (which is part of the often fatphobic stigma caused by the only representation the disorders get being my 600 pound life lmao). Tbh I wish people remembered fat storage diseases (not sure what to call them but like. Diseases that cause your body to deposit abnormal amounts of fat in certain places) are visible disabilities (like lipomas, lipedema, adiposis dolorosum, epidural lipomatosis, and I'm sure there's plenty more because I'm 99 percent sure I have the "apple shaped" equivalent of lipedema with a huge painful fat deposit on my neck that burns when you touch it, as well as a huge fat deposit inside my spine that I've probably had since my teens. Yeah fat disorders are not fun) existed like I try to search lymphedema and epidural lipomatosis on Tumblr and it's like nobody has it but me and people who have since deactivated

i know what you're talking about because i'm pretty sure my ex's father had lymphedema in both of his legs which severely limited his mobility, although he used crutches to get around and not compression wear.

the thing is, i wasn't saying that compression stockings don't help people get around. they do even in the case of people who have POTS or orthostatic hypotension (or autonomic failure.) bug mobility aids are designed with the purpose of assisting in movement. it's not contextual usage. canes (including white canes and not including decorative ones for casual use, which aren't supposed to support weight anyways), crutches, various types of scooters, wheelchairs, rollators, walkers, leg prosthetics, and guide dogs are all examples of things designed for the purpose of assisting in movement. some mobility aids that have both "mobile" and not mobile forms are standing aids and transfer aids (such as sling lifts and lift chairs.) technically stair lifts, ramps, and bars to help you stand up in handicap stalls are also mobility aids, although the way most people use the term probably doesn't suggest that. what unites all of the above is that they're intentionally and explicitly designed for mobility assistance. certain types of orthoses/braces are arguably mobility aids, but not all of them.

basically, all mobility aids help people move around, but not everything that can help someone move around is considered a mobility aid. i think this is an important distinction to make because mobility aid usage comes with a certain stigma all on their own, including mobility aids that you don't carry around with you (although the stigma when it comes to things like stair lifts or hand bars or ramps usually present as exclusion of access when it's needed, or those things not even being present.) mobility aids aren't exclusively designed or used by physically disabled people because we all know able-bodied people with temporary injuries use them, but the stigma around their usage, of course, stems from physical disability.

something like compression wear isn't inherently subject to the same stigma, although it definitely could be stigmatized in relation to certain body types and forms of disability, as you mentioned here. pain medications that contextually help people physically get around are certainly stigmatized and that stigma may overlap in some superficial ways to, say, getting around with a cane or chair or whatever, but overall it's a different type of stigma. you can personally consider something in your disability situation as a mobility aid, but that doesn't mean it is socially or medically recognized as such, which makes general claims like "compression stockings are a mobility aid" untrue, while "compression stockings help me walk" certainly can be true if that's the case. it's the difference between something explicitly meant to assist mobility vs. something that sometimes can.

generally, certain things can be thought of as a "mobility aid" in certain circumstances if you use the term very literally, but in a broader sense of the term, they aren't. it's more a matter of the stigma around mobility aid usage than semantics though. i hope all of that makes sense. no one has to agree with me, but that's the logic behind my thoughts.

also, this makes me wish i mentioned lymphedema and similar conditions in my post about people who "move wrong" due to their disabilities 'cause i tried to go out of my way to include conditions that are seldom talked about. i'm sorry that you don't have anyone to share your experiences with on tumblr. it must be painfully isolating and no one deserves that.

[greenokapi]

When it’s almost 9am and you haven’t slept cause you couldn’t stop watching pimple popping and lipoma removal videos while eating laufabrauð and now you have a headache and are probably gonna have weird fuckin dreams…

[thisisnotreallife]

The Cancer Journals, Part XI:

Finding My Cancer//Leaving Behind 2024

Today is the last day of 2024, which will now forever be the year I got diagnosed with breast cancer.

Many of us spend the last day of the old year reflecting on the months that have passed, which is something I am feeling particularly resistant to this New Year’s Eve.

It’s been a hard year.

I don’t want to remember mouth sores or bone aches from chemotherapy drugs. I don’t want to reflect on the moments that stretched into days between finding out I had cancer and finding out it wasn’t a cancer that I would be dying of imminently. I can’t remember much of the days I spent awake, but in an opioid-induced lack of lucidity, post-mastectomy; Patrick recalls conversations I was actively involved in that I have no memory of, and it is an eerie feeling.

What I do think is worth reflecting on, though (and more importantly sharing, too), is how my cancer was found this year—which is the only reason (thanks be!) that I am able to leave it behind in 2024.

In January of 2023, I saw a bump in the vicinity of my left armpit/side of my chest while in downward dog. I made an appointment with my primary care doctor for my annual wellness visit, which was overdue by a month; I had seen her two Decembers prior concerned about a lump in my right armpit that turned out to be a boil, likely caused by the oil-heavy natural deodorants I’ve used for the past fifteen years. (Cute.)

My doctor, though obviously skeptical at the back-to-back lumps-in-armpits appointments, felt around on my left side, found it, and sent me to get a mammogram and an ultrasound.

The radiologist determined it was a lipoma—just an accumulation of fatty tissue in my left armpit. Benign.

But in my “extremely dense breast tissue” (how does one cite MyChart when quoting directly? I reckon there’s an MLA rule for that…) on my right side, the doctor saw what are called “calcifications”—tiny clusters showing up as a whiteness on the mammogram scans that could lead to something. She recommended monitoring with mammograms every six months for the next two years even though I was only 36.

If I had known then what I know now—that dense breast tissue is considered a risk factor for developing cancer, both because the density of the tissue makes it difficult for radiologists to detect suspicious areas in mammography images and because (we think) women with dense breast tissue are more likely to develop breast cancer—I would have requested more imaging at the time. I would have demanded a 3D mammogram, which is a much more effective means of detecting cancers in dense breast tissue. I would have been more consistent each month at self-breast exams, which prior to my diagnosis, I would remember to do about half the time.

But they told me that calcifications are usually nothing to worry about, and so I didn’t. I came back, dutifully, in July of 2023 for a follow-up mammogram, at which time the radiologist didn’t notice any changes in the calcifications and told me to return in January.

We moved across the state in October, from Richland to Vancouver, and I neglected (like I always do) to establish new care with area doctors.I’ll do it when I need to, I always think. Who wants to wade through those insurance company websites, anyway?  

In early January, just after I discovered that I’d need to schedule a new patient appointment with a primary care doctor who would need to send a new order for a mammogram to a local imaging center before I could get my scan, I found out that I was pregnant—and they don’t do mammograms when you’re pregnant, at least not in the first trimester.

Neither my new primary care doctor nor my midwives seemed too concerned that we’d have to wait for the follow-up for a few months, and Patrick and I turned our attention to the ways our lives would be changing come September.

In early February, when I lost the pregnancy, getting a mammogram was the furthest thing from my mind, and I don’t think I thought about a self-breast exam for months.

If I had known then what I know now—that the growth of hormone-positive breast cancer can accelerate greatly after the surge of hormones that happens during pregnancy—I would have done things differently. I would have been vigilant about noticing changes in my breasts as soon as I saw those two faint lines on the stick that I’d unceremoniously peed one night in early January. If I had, I could have found it even earlier than I did.

After my miscarriage, I tried to focus on “getting better”—both physically and emotionally. As the weeks and months passed, I didn’t feel like I was getting better, but I didn’t feel like I had cancer, either. I had trouble focusing on conversations I was having. I had trouble focusing, literally, when shifting my gaze from somewhere close up to somewhere far away. I felt disconnected from myself in a way I couldn’t articulate. I just felt off.

I assumed it was, for lack of better phrasing, a miscarriage hangover—that I was in a funk I’d come out of, eventually.

In the spring, I decided to make an effort to “get back to normal” by contacting my doctor to get the ball rolling on my overdue mammogram. Insurance requirements meant that she’d need to see me for a breast exam before placing the imaging order, and so I made an appointment in late April for a few weeks later, in the last week of May.

On her exam table, she found a lump in my right breast, in the densest part of the tissue—but said it wasn’t anything she was particularly worried about, and I was going to be getting that mammogram anyway.

That night, I even forgot to tell Patrick what she’d found, she’d seemed so nonchalant about it.

When I went in for the mammogram in early June, they sent me home when I told them there was a chance that I could be pregnant, since I hadn’t returned to any birth control after miscarrying. We rescheduled for two weeks later, on the summer Solstice, with the understanding that I’d be unable to get the scan then unless I knew definitively I was not pregnant.

I wasn’t, and so we did the mammogram. And then the ultrasound.

And then the radiologist came to see me in the tiny dressing room and told me she was recommending a biopsy on the mass my doctor had found four weeks earlier and I could feel the blood draining out of my face and had to force myself to pay attention to the words she was saying instead of the feeling of hot and then cold sweeping down from the crown of my head toward my heart, toward the lump in my breast.

When she left, I got dressed and walked outside to the car to tell Patrick.

I texted my sister, the doctor, along the way. I wanted to know how often biopsies came back negative, but the radiologist wouldn’t give me numbers, and my sister told me not to worry, too.

I did 108 sun salutations and tried not to worry.

I went back to the same ultrasound room for the biopsy on June 28th, a Friday, and they needed extra anesthesia to numb me fully before I couldn’t feel anything as the biopsy needle jammed into my breast one, two, three, eight times to take core samples of the lump at its center.

I went home sore and made cornmeal strawberry shortcake for the two of us. While it baked, I tried to lie in our hammock and release worries about the biopsy, with our cat Troll Boy meowing loudly under me for reasons I couldn’t figure out until the rope tying the hammock to the tree snapped, and I fell with the hammock to the ground.

I shoulda known I had cancer then.

I had my suspicions, though.

In June, I’d started to notice scratches and cuts taking longer to heal than normal and any bruises I’d get in the normal course of my life (I bruise easily and often joke that I can’t distinguish well between where my body ends and the world begins) had begun taking on a deep, frightening purplish hue and sticking around for a lot longer than usual.

We didn’t have to wait long for my suspicions to bear out, and I got a phone call from my doctor at 5:03pm on Monday, July 1st, as we were driving home from a day trip to Seattle to distract ourselves from the pending results. We still had an hour and a half drive ahead of us after the call.

And that, my friends, is how we found my cancer.

In retrospect, I have to wonder if my body was trying to tell me something, causing benign lumps to form in places I’ve always been told to pay attention to.

If I hadn’t gone to see my doctor about that lipoma, the radiologist never would have found the calcifications, which would have meant that I wouldn’t have been on a biannual mammogram schedule. Annual mammograms are supposed to begin at 40 in the U.S.—I turned 38 in September of this year—and so without these reasons to be squeezing and scanning and checking almost four years early, it’s possible I wouldn’t have found the cancer until it was too late.

If everything had been the same except that I hadn’t insisted on seeing somebody about a lump that turned out to be nothing two years ago, the cancer could have kept growing after my miscarriage and spread past the first lymph node Dr. Storm found, into my lungs. My liver. My brain.

I’ve shared before that I have no family history of breast cancer, and that when my oncology team ordered a genetics test to look for any mutations that may have led to the development of my cancer, the tests came back negative.

That leaves environmental factors (impossible to determine a causal relationship, and irrespective of my attempts to avoid carcinogenic environmental risks…) and sheer, dumb luck. The same sheer, dumb luck that caused me to be born in the United States instead of somewhere in the developing world.

When we met with Dr. Storm over the summer and reviewed my scans with her, she pointed to a vague spot on the July 2023 mammogram, near the calcifications, and said, “It’s not fair, because I have the scans that show me where the tumor is now—but I can kinda sorta see something forming here.”

I’ll never know what caused my cancer, or how long it had been growing inside of me before Dr. Storm excised it from my body in November.

But at our first appointment, when I gave her my family medical history and told her about my mother’s suicide in 2021 and my brother’s incarceration for murder, she nodded and said something about the mind-body connection. All that trauma has to go somewhere—and I hadn’t even told her about the early stuff.  

The reality is, it doesn’t matter what caused my cancer, or when it started. Who gets cancer and who doesn’t is completely random—and with over 40% of the U.S. population expected to get a cancer diagnosis in our lifetimes and one in eight women receiving a breast cancer diagnosis, fairly common.

What matters—to me, anyway, on the cusp of a new year that I will be starting cancer-free—is that it’s out.

Happy New Year, folks. 🍾 🥂

Oh, and: if you haven’t checked your chest this month, get your self-exam in today. There’s still a couple of hours left in 2024. 🎆

(And psst…be sure to advocate for yourself if you feel anything is off!)

[smartsurgeons]

Understanding the Causes and Risk Factors of Lipomas: A Comprehensive Guide

Lipomas are non-cancerous tumors composed of fatty tissue. While these benign lumps are common and usually harmless, learning about their causes and risk factors can help you manage and prevent their development. In this post, we will explore the causes behind lipomas and highlight the risk factors that may contribute to their formation. For personalized advice and guidance, you can always consult with lipoma specialists to better understand your symptoms and explore treatment options, including lipoma removal without surgery.

What Exactly is a Lipoma?

A lipoma is a soft, rubbery lump that forms beneath the skin, made up of fat cells. These growths tend to grow slowly and are generally harmless, though they can cause discomfort or become a cosmetic concern for some people. Lipomas can develop anywhere on the body, with common areas being the shoulders, neck, back, and arms. While lipomas are typically painless, in some cases, individuals may seek professional help from lipoma surgery specialists if the growth causes issues like pain or aesthetic concerns.

Common Causes of Lipomas

Several factors contribute to the formation of lipomas. Some of these causes are genetic, while others may be linked to hormonal changes or physical trauma. Here's an overview of the most common causes:

Genetic Factors: The Role of Family History and Inherited Conditions

Inherited Disorders: A family history of lipomas can increase your likelihood of developing them. Familial multiple lipomatosis, a rare genetic disorder, causes multiple lipomas to form throughout the body. If someone in your family has this condition, you may be at higher risk.

Genetic Predisposition: Having a family member with lipomas also increases your chances of developing them due to shared genetic traits.

Cellular Growth and Mutation: How Fat Cells Contribute to Lipoma Development

Uncontrolled Fat Cell Growth: Lipomas occur when fat cells begin to grow uncontrollably under the skin. The exact cause behind this abnormal growth isn't fully understood, but it is believed to be related to disruptions in cell regulation and growth.

Genetic Mutations: Changes in certain genes may trigger the abnormal growth of fat cells, leading to the development of lipomas.

The Impact of Trauma: Injury and Physical Impact

Although physical injury or trauma isn't generally considered a primary cause of lipomas, some individuals report developing lipomas after an injury to the affected area. However, there is no solid evidence suggesting that trauma directly causes lipomas, making it more likely a coincidence.

Hormonal Influence: How Fluctuations in Hormones Can Play a Role

Hormonal changes may influence lipoma formation. Some people notice lipomas appearing or growing during periods of hormonal fluctuations, such as puberty, pregnancy, or menopause. However, more research is needed to fully understand the link between hormones and lipomas.

Identifying the Risk Factors for Lipomas

While genetics and cellular changes play a key role in lipoma development, certain risk factors may increase the likelihood of developing these benign tumors. Let's take a look at the most common risk factors.

Age: Most Common in Middle-Aged Adults

Lipomas are most frequently diagnosed in adults aged 40 to 60. Although they can occur at any age, they are rare in children and teenagers. If you're within this age range, you may be more likely to develop lipomas.

Gender: Do Men and Women Have the Same Risk?

Interestingly, lipomas affect both men and women equally, meaning gender does not appear to play a significant role in their development.

Obesity: Does Being Overweight Increase Your Risk?

While obesity isn't a direct cause of lipomas, individuals who are overweight may have a slightly increased risk of developing them. Excess fat tissue could potentially contribute to lipoma formation, although further research is necessary to understand this relationship fully.

Underlying Medical Conditions: How Certain Health Issues Increase Risk

Genetic Syndromes: Certain hereditary conditions, such as Gardner's syndrome and Cowden syndrome, are associated with an increased risk of developing lipomas. These syndromes typically come with additional health issues that require specialized medical care.

Diabetes: Some studies suggest a possible connection between diabetes and the development of lipomas, though the exact nature of this relationship remains unclear.

Family History: The Genetic Link to Lipomas

As discussed earlier, having a family history of lipomas increases your chances of developing them yourself. In particular, familial multiple lipomatosis is a hereditary condition that raises the risk of lipoma formation significantly.

Lifestyle Factors: Diet, Exercise, and Prevention

Although no direct connection has been established between diet, exercise, and lipomas, maintaining a healthy lifestyle is always beneficial. Good nutrition and regular physical activity can promote overall health and help prevent a wide range of benign tumors, including lipomas.

When to Seek Help: Recognizing the Signs That Require Attention

In most cases, lipomas do not require treatment, as they are benign and harmless. However, you should seek medical attention if:

Pain or Discomfort: The lipoma becomes painful or irritating.

Rapid Growth: The lump increases in size or changes shape quickly.

Cosmetic Concerns: The appearance of the lipoma causes self-esteem or cosmetic concerns.

Uncertainty: You are unsure if the lump is a lipoma or something else, such as a different type of tumor.

A lipoma specialist can assess the lump, conduct necessary tests, and determine whether any further treatment is needed.

Exploring Treatment Options: Can Lipomas Be Treated Without Surgery?

If you decide to remove a lipoma, you have several treatment options, depending on the size, location, and symptoms: Surgical Removal: This is the most common treatment method, involving an incision to remove the lipoma. The procedure is usually performed on an outpatient basis under local anesthesia.

Liposuction: For some lipomas, liposuction may be used to remove the fatty tissue. A thin tube is inserted into the lipoma, and the fat is suctioned out.

Steroid Injections: In certain cases, steroid injections may be administered to shrink the lipoma, though this is a less common approach.

If you're interested in non-invasive options, lipoma removal without surgery may be a viable choice. Liposuction or steroid injections might be effective alternatives depending on the nature of the lipoma.

Final Thoughts: Managing and Preventing Lipomas

While lipomas are generally benign and pose minimal health risks, understanding their causes and risk factors can help you stay proactive in managing them. Genetics, hormonal changes, trauma, and underlying medical conditions all play a role in lipoma development. While there is no guaranteed way to prevent lipomas, adopting a healthy lifestyle and being mindful of your family history may help reduce your risk.

If you notice any unusual lumps or changes in your skin, consult with lipoma specialists for proper diagnosis and guidance on treatment options, including lipoma removal without surgery. Reach out to Smart Surgeon for expert care and treatment options for lipomas. Visit their website for more information.

[thesoftestpunk]

Got a call with some results! Recommended physical therapy specifically for my hip issues instead of my back. If that doesn’t work then we have to consider surgery 🫡

As for my back, they found a lipoma but I’ve had that spot since I was a kid bc of my spina bifida but getting another mri specifically to check it out and meeting w a spine specialist. Idk if it’s causing issues but 🤷🏼‍♀️

[heaalth]

Gynecomastia Pinch Test

Gynecomastia Pinch Test: A Quick Guide to Detect Male Breast Tissue Growth

Gynecomastia Pinch Test - Gynecomastia is a medical condition characterized by the enlargement of male breast tissue due to a hormonal imbalance between estrogen and testosterone. While it is generally harmless, gynecomastia can cause emotional distress and self-consciousness. Detecting the condition early is crucial for addressing it effectively. One of the simplest and most common self-diagnostic methods is the Gynecomastia Pinch Test.

What Is the Gynecomastia Pinch Test?

The pinch test is a self-assessment technique that helps identify whether the enlargement of the chest area is due to gynecomastia (excess glandular tissue) or pseudogynecomastia (fat accumulation caused by obesity). It involves physically examining the chest to differentiate between glandular tissue and fatty tissue.

How to Perform the Gynecomastia Pinch Test

Here is a step-by-step guide to conducting the pinch test:

Stand in Front of a Mirror: Remove your shirt and stand upright in front of a mirror. This allows you to observe any visible signs of asymmetry, swelling, or breast enlargement.

Use Your Fingers to Pinch the Area Around the Nipple: Using your thumb and index finger, gently pinch the area around your nipple. Be cautious not to press too hard, as this may cause discomfort.

Feel for the Type of Tissue:

Glandular Tissue: If you feel a firm, rubbery disk or lump beneath the nipple area, it is likely glandular tissue, indicating gynecomastia.

Fatty Tissue: If the area feels soft and lacks a distinct lump, the enlargement is likely due to excess fat, a condition referred to as pseudogynecomastia.

Repeat on the Other Side: Gynecomastia can affect one or both breasts. Ensure you perform the test on both sides to detect any asymmetry.

Limitations of the Pinch Test

While the gynecomastia pinch test is a useful preliminary method, it has its limitations:

Subjectivity: It can be difficult to distinguish between fatty tissue and glandular tissue without prior experience or training.

Similar Symptoms: Conditions such as lipomas (fatty tumors) or breast cancer can sometimes mimic gynecomastia.

Uncertain Diagnosis: A positive result does not confirm gynecomastia definitively. Medical tests such as ultrasound or mammography may be required for an accurate diagnosis.

When to See a Doctor

If you notice any of the following, it’s best to consult a healthcare professional:

Persistent breast enlargement for more than six months.

Pain, tenderness, or swelling in the chest area.

Asymmetry or a significant lump in one breast.

Sudden enlargement during puberty or adulthood without any apparent reason.

Treatment Options for Gynecomastia

If diagnosed with gynecomastia, treatment options vary based on the severity and underlying cause:

Observation: In cases where gynecomastia occurs during puberty, it often resolves on its own without intervention.

Medications: Hormonal therapy or other medications may help address the imbalance.

Surgery: For severe or persistent cases, surgical intervention such as liposuction or gland excision may be recommended.

Conclusion

The gynecomastia pinch test is a quick and simple method for assessing male breast tissue growth. While it provides a preliminary understanding, professional medical evaluation is essential for a confirmed diagnosis and effective treatment. Early detection and consultation with a healthcare provider can help address gynecomastia and its psychological impact efficiently.

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Gynecomastia Pinch Test: A Detailed Guide to Understanding and Detecting Male Breast Enlargement

Gynecomastia is a medical condition characterized by the abnormal enlargement of male breast tissue due to an imbalance in hormones, particularly an increase in estrogen relative to testosterone. While it is a benign condition, it can cause significant emotional and psychological distress in affected individuals. Detecting gynecomastia early can help address the condition effectively, whether through lifestyle changes, medications, or medical procedures. One of the simplest self-assessment methods to identify gynecomastia is the Gynecomastia Pinch Test.

This article will explain what the pinch test is, how to perform it, its limitations, and the steps you should take if you suspect gynecomastia.

What Is the Gynecomastia Pinch Test?

The gynecomastia pinch test is a self-assessment technique that helps differentiate between gynecomastia (enlarged glandular tissue) and pseudogynecomastia (fat accumulation in the chest area due to obesity). It involves physically examining the chest to feel for the type of tissue beneath the nipple area.

The test is particularly useful for people who are unsure whether their chest enlargement is due to hormonal changes or weight-related fat deposits. While not a definitive diagnostic method, the pinch test is a valuable first step in determining whether medical evaluation is necessary.

How to Perform the Gynecomastia Pinch Test

Performing the pinch test is simple and can be done at home. Follow these steps for an accurate self-assessment:

1. Prepare for the Test

Stand in front of a mirror in a well-lit room.

Remove your shirt to expose your chest. This allows you to observe any visible differences or abnormalities in the chest area, such as swelling, asymmetry, or puffiness around the nipples.

2. Use Your Fingers to Pinch the Nipple Area

With one hand, place your thumb and index finger around the nipple and gently pinch the tissue.

Apply light pressure and feel for any underlying structure. Avoid pressing too hard, as it may cause discomfort or obscure the results.

3. Assess the Tissue

Glandular Tissue (Gynecomastia): If you feel a firm, rubbery lump or disk-like tissue directly beneath the nipple, this is likely glandular tissue and could indicate gynecomastia.

Fatty Tissue (Pseudogynecomastia): If the tissue feels soft and lacks a distinct lump, it is more likely to be fat accumulation, commonly seen in overweight or obese individuals.

4. Check Both Sides

Gynecomastia can affect one or both sides of the chest. Repeat the test on the other side to look for symmetry or differences.

What to Look for During the Pinch Test

While performing the pinch test, pay attention to the following signs:

Firm Lump: A rubbery lump beneath the nipple indicates glandular tissue growth, often associated with gynecomastia.

Pain or Tenderness: Tenderness or sensitivity in the nipple area can be a sign of gynecomastia, especially during the early stages.

Asymmetry: Gynecomastia may affect one breast more than the other, leading to visible asymmetry.

Puffy Nipples: Swelling or puffiness around the areola (the darker skin surrounding the nipple) is a common symptom of gynecomastia.

Understanding the Results

The gynecomastia pinch test is a helpful tool for identifying potential symptoms, but it is not a conclusive diagnostic method. Here’s what your findings might mean:

Positive for Glandular Tissue: If you detect a firm lump beneath the nipple, you may have gynecomastia.

Soft and Fatty Tissue: This suggests pseudogynecomastia, which is more related to weight gain and can often be addressed through diet and exercise.

Pain or Swelling Without a Lump: This could indicate other conditions, such as an infection or hormonal imbalance, and should be evaluated by a doctor.

Limitations of the Pinch Test

Although the gynecomastia pinch test is a simple and useful self-assessment method, it has its limitations:

Subjectivity: The test relies on an individual’s ability to differentiate between glandular and fatty tissue, which can be difficult without prior experience.

Overlap with Other Conditions: Conditions like lipomas (benign fatty tumors), cysts, or even breast cancer can mimic the symptoms of gynecomastia.

Confirmation Requires Medical Tests: Even if the pinch test indicates gynecomastia, a medical evaluation using tools like ultrasound, mammography, or hormonal blood tests is required to confirm the diagnosis.

When to Seek Medical Attention

If the pinch test suggests gynecomastia or you experience any of the following symptoms, it’s important to consult a healthcare professional:

Persistent breast enlargement lasting more than six months.

Pain, tenderness, or swelling in the chest area.

A sudden increase in breast size without a clear cause.

A lump that feels hard or grows rapidly.

Nipple discharge or changes in skin texture.

Causes of Gynecomastia

Understanding the underlying causes of gynecomastia can help in its diagnosis and treatment. Common causes include:

Hormonal Imbalance: An increase in estrogen or a decrease in testosterone is the primary cause.

Medications: Certain drugs, such as anti-androgens, anabolic steroids, and antidepressants, can trigger gynecomastia.

Underlying Health Conditions: Liver disease, kidney failure, or thyroid disorders may contribute to hormonal imbalances.

Substance Use: Alcohol, marijuana, and anabolic steroids can increase the risk of gynecomastia.

Treatment Options for Gynecomastia

If diagnosed with gynecomastia, treatment options vary depending on its severity and underlying cause:

Lifestyle Changes: Weight loss and regular exercise can help reduce fat accumulation in cases of pseudogynecomastia.

Medications: Hormonal therapy or medications such as tamoxifen may be prescribed to address glandular growth.

Surgical Intervention: Severe or persistent cases of gynecomastia may require surgical procedures such as liposuction or glandular tissue excision to restore the chest’s appearance.

Conclusion

The gynecomastia pinch test is a quick and easy method to self-assess male breast enlargement. While it provides valuable initial insights, it is not a definitive diagnostic tool. If you suspect gynecomastia based on the pinch test or experience persistent symptoms, consulting a healthcare professional is essential for accurate diagnosis and appropriate treatment.

By understanding the pinch test and seeking timely medical evaluation, individuals can address gynecomastia effectively and alleviate any physical or emotional discomfort associated with the condition.