#treating rhabdomyosarcoma

[bcisurat]

Childhood Cancer- Myths and Facts: What You Need to Know?

Paediatric cancer is a deeply concerning issue that touches the lives of many families around the world. Paediatric cancer specialists in Surat worry that despite advancements in medical research and treatment several myths about paediatric cancer persist, causing unnecessary fear and misunderstanding. Addressing these myths with factual information is crucial for supporting affected families and promoting awareness. Here are some common myths about paediatric cancer busted by our experts from BCI- Blood and Cancer Institute, one of the best cancer hospitals in Surat, and the facts that dispel them.

Myth 1: Paediatric Cancer is Extremely Rare

Fact: While paediatric cancer is less common than adult cancer, it is still a significant health concern. Each year, thousands of children are diagnosed with various types of cancer, including leukaemia, brain tumours, and lymphomas. Cancer specialists in Surat are of the opinion that awareness and funding for research are essential to continue improving treatment options and survival rates for these young patients.

Myth 2: Paediatric Cancer is Always Fatal

Fact: Advances in medical research and treatment have significantly improved the prognosis for many types of paediatric cancer. While it remains a serious illness, the survival rates for childhood cancers have increased dramatically over the past few decades. Today, the five-year survival rate for paediatric cancer is approximately 84%, thanks to early detection, innovative treatments, and comprehensive care. It’s important to provide hope and support to families facing a paediatric cancer diagnosis, knowing that many children go on to live healthy, fulfilling lives.

Myth 3: Paediatric Cancer is Preventable

Fact: Unlike many adult cancers, paediatric cancers are not typically linked to lifestyle or environmental factors. The exact causes of most paediatric cancers remain unknown, and they are not considered preventable. Researchers believe that genetic mutations or abnormalities that occur early in a child’s development might play a significant role. While ongoing research aims to better understand the causes, it is crucial to recognize that parents and caregivers are not to blame for their child’s illness.

Myth 4: Paediatric Cancer Symptoms are Easy to Identify

Fact: The symptoms of paediatric cancer can often mimic those of common childhood illnesses, making early detection challenging. Symptoms such as fatigue, fever, bruising, and weight loss are not specific to cancer and can be attributed to various other conditions. This can lead to delays in diagnosis and treatment. Regular check-ups and prompt medical attention for persistent or unusual symptoms are vital in ensuring early detection and effective treatment, says our paediatric cancer specialist in Surat at BCI- Blood and Cancer Institute.

Myth 5: Paediatric Cancer Treatments are the Same as Adult Treatments

Fact: Cancer treatments for children in Surat are often different from those used to treat adult cancers. Children’s bodies respond differently to cancer and its treatments, necessitating specialized approaches. Paediatric oncologists develop tailored treatment plans that consider the unique needs of young patients, focusing on minimizing side effects and promoting long-term health. These plans may include a combination of chemotherapy, radiation therapy, surgery, and newer targeted therapies.

Myth 6: All Paediatric Cancers are the Same

Fact: Paediatric cancer encompasses a wide range of diseases, each with its own characteristics and treatment protocols. The most common types of paediatric cancer include leukaemia, brain and spinal cord tumours, neuroblastoma, Wilms tumour, lymphoma, and rhabdomyosarcoma. Each type requires a specific approach to diagnosis and treatment. Understanding the diversity of paediatric cancers and cancer treatment in Surat is essential for providing accurate information and support to affected families.

Myth 7: Paediatric Cancer Only Affects the Child

Fact: Paediatric cancer impacts the entire family, not just the child diagnosed with the disease. Parents, siblings, and extended family members all experience emotional, physical, and financial strain. The journey through diagnosis, treatment, and recovery requires a strong support system and access to resources such as counselling, support groups, and financial assistance programs. Recognizing the broader impact of paediatric cancer can help communities and healthcare providers offer comprehensive support to families in need.

Conclusion

Dispelling myths about paediatric cancer is crucial for fostering understanding, providing accurate information, and supporting affected families. Paediatric cancer, while less common than adult cancer, remains a significant health concern that requires ongoing research, funding, and awareness. Advances in treatment have greatly improved survival rates, offering hope to many children and their families. Understanding that paediatric cancer is not preventable and recognizing the unique challenges it presents can help alleviate unnecessary guilt and fear. By addressing symptoms promptly and supporting specialized treatments, we can continue to improve outcomes for young cancer patients.

Educating ourselves and others about the realities of paediatric cancer empowers us to be better advocates and supporters. Through continued awareness and support, we can contribute to the ongoing efforts to find cures and improve the lives of children affected by this disease. Together, we can create a more informed and compassionate community for all families facing paediatric cancer.

[drpurvikadakiakutty]

In the Hands of Care: Dr. Purvi Kadakia Kutty, Leading Child Oncologist in Kharghar    

Pediatric Oncology is a specialized branch of medicine that focuses on the diagnosis, treatment, and management of cancer in children and adolescents. It deals specifically with Child Oncologist  in navi mumbai, which can vary significantly from cancers aggressiveness, and treatment approaches. Pediatric oncologists are medical experts who provide comprehensive care to young patients with cancer, working closely with a multidisciplinary team to ensure the best possible outcomes and quality of life for these young patients and their families.

Conditions Treated in Pediatric Oncology:

Pediatric oncologists manage various types of childhood cancers, which can affect different parts of the body. Some common childhood cancers treated in Pediatric Oncology include:

Leukemias: Cancers that affect the bone marrow and blood, including Acute Lymphoblastic Leukemia (ALL) and Acute Myeloid Leukemia (AML).

Lymphomas: Cancers that arise from the lymphatic system, such as Hodgkin's lymphoma and Non-Hodgkin lymphoma.

Brain Tumors: Tumors that develop in the brain or spinal cord, including astrocytomas, medulloblastomas, and ependymomas.

Sarcomas: Tumors that arise from bone, muscle, or soft tissues, such as osteosarcoma, rhabdomyosarcoma, and Ewing sarcoma.

Neuroblastoma: A cancer that develops from immature nerve cells and typically occurs in young children.

Wilms Tumor: A type of kidney cancer that primarily affects children.

Retinoblastoma: A rare eye cancer that typically develops in early childhood.

Germ Cell Tumors: Tumors that arise from germ cells, commonly found in the ovaries or testes.

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

Diagnostic Tests in Pediatric Oncology:

To diagnose Child Oncologist, pediatric oncologists may utilize a range of diagnostic tests, including:

Biopsy: A procedure to obtain a tissue sample for examination under a microscope to determine if cancer cells are present.

Imaging Studies: Techniques like X-rays, CT scans, MRI, and PET scans are used to visualize tumors and evaluate the extent of cancer.

Bone Marrow Aspiration and Biopsy: These tests help assess if cancer has spread to the bone marrow.

Lumbar Puncture (Spinal Tap): A procedure to collect cerebrospinal fluid for evaluation if cancer involves the central nervous system.

Pediatric Oncology Services: 

Diagnosis and Staging: Comprehensive evaluation and accurate diagnosis of childhood cancers, including the use of imaging studies, biopsies, and laboratory tests to determine the type and stage of cancer.

Treatment Planning: Individualized treatment plans tailored to the specific type of childhood cancer, its stage, and the child's overall health. Treatment options may include surgery, chemotherapy, radiation therapy, immunotherapy, targeted therapy, and stem cell transplantation.

Chemotherapy: Administration of anti-cancer drugs to kill or slow the growth of cancer cells.

Radiation Therapy: Use of high-energy radiation to target and destroy cancer cells.

Stem Cell Transplantation: Replacement of damaged bone marrow with healthy donor cells in certain cases.

Immunotherapy: Treatment to boost the body's immune system to recognize and attack cancer cells.

Supportive Care: Management of cancer-related symptoms and side effects, as well as addressing the emotional and psychosocial needs of the child and their family.

Long-term Follow-up: Monitoring the child's progress after completing cancer treatment, detecting any signs of cancer recurrence, and providing ongoing support and survivorship care.

Dr. Purvi Kadakia Kutty's dedication to oncology and her unwavering commitment to her patients make her one of the best oncologists in Kharghar. Her extensive training, compassionate care, and holistic approach to treatment ensure that her patients receive the best possible care during their most challenging times. Dr. Kutty stands out as a beacon of hope and excellence in the field of oncology.

Visit: https://childoncologist.com/ 

Contact: +91 77381 62020

[blog-site-for-market-research]

Share Insights: Navigating the Eye Cancer Market Landscape

Market Overview –

During the projection period of 2022–2030, the eye cancer market is expected to grow at a rate of 8.60% CAGR to reach USD 16,955.10 million by 2030.

The eye cancer market pertains to the segment of the healthcare industry focused on the diagnosis, treatment, and management of ocular malignancies. Eye cancer, also known as ocular cancer, includes various types of tumors that can affect different structures of the eye, such as the retina, iris, choroid, and orbit. This market encompasses a range of diagnostic tools, treatment modalities, and supportive care options tailored to the specific needs of patients with eye cancer.

One of the primary drivers of the eye cancer market is the increasing incidence of ocular malignancies worldwide. Factors such as aging populations, environmental exposures, genetic predispositions, and advancements in diagnostic imaging have contributed to the rising prevalence of eye cancer, prompting a greater demand for effective treatment options.

Moreover, advancements in medical technology and treatment approaches have revolutionized the management of eye cancer, leading to improved outcomes and survival rates for patients. Innovative therapies such as targeted molecular therapies, immunotherapies, and proton beam therapy offer promising alternatives to traditional treatments like surgery and radiation therapy, providing patients with more options for personalized care.

The COVID-19 pandemic has impacted the eye cancer market, with disruptions in healthcare services, delayed diagnoses, and changes in treatment protocols. However, the pandemic has also highlighted the importance of telemedicine and remote consultations in providing continuity of care for patients with eye cancer, facilitating access to specialized expertise and support services.

Despite challenges such as limited awareness about eye cancer, disparities in access to healthcare, and the high cost of advanced treatments, the eye cancer market is expected to grow as research efforts continue to improve understanding, diagnosis, and treatment of ocular malignancies. With ongoing innovation and collaboration among healthcare providers, researchers, and industry stakeholders, the eye cancer market holds promise for better outcomes for patients with eye cancer in the future.

The eye cancer market is evolving, with a focus on innovative treatments for conditions like eye melanoma. As awareness grows and diagnostic capabilities improve, there's a rising demand for targeted therapies and precision medicine approaches. Advances in surgical techniques, radiation therapy, and immunotherapy offer hope for improved outcomes in treating eye cancer, driving research and development efforts in the market.

Ongoing research and development efforts focus on targeted therapies and immunotherapies tailored to specific types of eye cancer, thereby improving patient outcomes. Additionally, collaborations between healthcare organizations, research institutions, and pharmaceutical companies play a crucial role in advancing treatment options and expanding market reach. However, challenges such as late-stage diagnosis, limited access to specialized care in remote areas, and the high cost of treatment pose significant barriers to market growth.

Segmentation –

The global market is segmented on types, treatment and end users. On the basis of types, the market is segmented into intraocular cancer, squamous cell cancer, rhabdomyosarcoma, and others. Intraocular cancer is further segmented into melanoma of the eye, lymphoma of the eye, and cancers in children. On the basis of treatment, the market is categorised into chemotherapy, surgery & radiation therapy, targeted therapy, hormone therapy, biologic therapy, and other.

Chemotherapy is further segmented into anthracyclines, taxanes, antimetabolites, and alkylating agents. Target therapy is sub segmented into monoclonal antibodies and tyrosine kinase inhibitors. Hormone therapy is further segmented into selective estrogen-receptor modulators (SERMs), aromatase inhibitors and others. On the basis of end users, the market is segmented into hospital & clinics, ambulatory care centers and others

Regional Analysis –

Regional analysis of the eye cancer market reveals disparities in incidence rates, diagnostic capabilities, and treatment options across different regions. In developed regions like North America and Europe, where there is a higher prevalence of eye cancers and advanced healthcare infrastructure, the market for eye cancer diagnosis and treatment is well-established, with a focus on early detection and multimodal therapy approaches. Conversely, in developing regions with limited access to specialized eye care services and oncology expertise, such as parts of Africa and Asia-Pacific, the market for eye cancer management is still evolving, with challenges related to late-stage diagnosis and treatment access. Moreover, cultural attitudes towards cancer screening and treatment impact patient behaviors and healthcare-seeking patterns across different regions. As awareness of eye cancer risks and treatment options increases globally, there is a growing opportunity for market expansion through collaborative efforts to improve early detection, access to care, and affordability of treatment modalities for eye cancer patients worldwide.

Key Players –

Eye cancer companies include Novartis AG (Switzerland), Spectrum Pharmaceuticals Inc. (U.S.), GlaxoSmithKline Plc. (U.K.), Bayer AG (Germany), Amgen, Inc. (U.S.), Bristol-Myers Squibb Company (U.S.), Eli Lilly and Company (U.S.), AstraZeneca Plc. (U.K.), F. Hoffmann-La Roche Ltd. (Switzerland), Janssen Biotech, Inc. (U.S.), Sanofi (France), AbbVie Inc. (U.S.), Takeda Pharmaceuticals (Japan), Pfizer, Inc. (U.S.), Merck & Co., Inc. (U.S.), Oncomed Pharmaceuticals (U.S.), and Immunomedics (U.S.). Related Reports –

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For more information visit at MarketResearchFuture

[virinchihospitals90]

Best Orthopedic surgeon in Hyderabad - Virinchi Hospitals

Virinchi Hospitals: Your Trusted Orthopedic and Spinal Care Center in Hyderabad

At Virinchi Hospitals, we understand that the backbone of a healthy life is a healthy spine. The numerous causes of back pain can often make life challenging. With our tag as the best hospital for back pain in Hyderabad, we are committed to providing personalized and advanced treatments for each patient.

Specialized Spinal Surgery Procedures Include:

Disc Surgery

Advanced Microsurgery for disc ailments

Fixation systems specially designed for fractures

Surgical correction of spinal deformities

Cutting-edge procedures for spinal tuberculosis

State-of-the-art endoscopic spine surgery

Holistic Arthritis Care: From Osteoarthritis and Rheumatoid arthritis to the less common Infective and Traumatic arthritis, our comprehensive care ensures patients lead a pain-free life.

Pediatric Orthopedics: Children have unique bone structures and issues. Our specialized services include treatments for:

Osteotomies for conditions like Knock knees and bowlegs

CTEV

Hip Dysplasia

Advanced fracture management with flexible nails

General Orthopedic Care at Virinchi Hospitals:

Comprehensive fracture and trauma care

Specialized hand and shoulder surgeries

Cutting-edge micro vascular procedures including nerve repair, and nerve and muscle grafts

Expert care for foot and ankle injuries

Best-in-class treatment for sports injuries and limb deformities

Pioneer in tumor surgeries for bone cancers such as osteosarcoma, Ewing’s sarcoma, chondrosarcoma, and soft tissue sarcomas like rhabdomyosarcoma.

Being recognized as the best orthopedic hospital in Hyderabad isn't just an honor; it's a testament to our unwavering commitment to excellence in patient care. And with the added reputation of performing the best arthroscopic surgery of the knee, we stand unmatched.

Arthroscopic Knee Surgery at Virinchi Hospitals: Our team of internationally trained orthopedic surgeons specializes in arthroscopic treatments. Before any surgical intervention, patients undergo a thorough diagnostic procedure, both conventional and arthroscopic. Post diagnosis, arthroscopic intervention is used to correct the knee condition, with a primary focus on restoring functionality and minimizing pain. Prior to surgery, we ensure patients are educated on the required precautions, surgery preparations, and post-operative care. Additionally, our doctors discuss potential risks associated with the surgery.

Conditions treated through Arthroscopic Surgery include:

Anterior Cruciate Ligament (ACL) tears

Articular cartilage damage

Knee fractures and sepsis

Loose bodies in the knee

Misaligned or dislocated patella/kneecap

Osteoarthritis of the knee

Popliteal cyst and much more

For those searching for the best orthopedic doctor in Hyderabad, the finest knee pain specialist in Hyderabad, or the top orthopedic surgeon in Hyderabad, Virinchi Hospitals is the answer. As the apex of orthopedic care, Virinchi Hospital remains committed to delivering excellence at every step. Your trust in our services drives our dedication.

Address: Virinchi Circle, Rd Number 1, Banjara Hills, Hyderabad, Telangana

Phone.no: 040 46999999

Website: https://virinchihospitals.com/orthopedics/

#best orthopedic hospital in Hyderabad #knee pain specialists in Hyderabad

#best orthopedic doctor in Hyderabad #Best Orthopedic surgeon in Hyderabad

[nikitas78ms]

Cancer in Kids and Teenagers

Cancer is a mind-boggling sickness that can influence anybody at whatever stage in life. In any case, there are a few distinctions between youth cancer and grown-up diseases, including the sorts of tumours that they will generally get, how they are analyzed and treated, and the drawn-out impacts they might confront.

Adolescence Cancer versus Grown-up Diseases

Adolescent cancer is those that happen in people younger than 18. The most widely recognized sorts of young life diseases incorporate leukaemia, cerebrum and spinal rope growths, neuroblastoma, Wilms cancer, and lymphoma. The reasons for youth diseases are not surely known, albeit a few hereditary and natural elements might assume a part.

Conversely, grown-up cancer is those that happen in people over the age of 18. The most widely recognized kinds of grown-up cancer incorporate bosom disease, cellular breakdown in the lungs, prostate malignant growth, colorectal disease, and bladder malignant growth. These tumours are more normal in more established grown-ups and are frequently brought about by way of life factors like smoking, liquor utilization, and less than stellar eating routine. It is difficult to detect cancer in the early stages. But if you even notice a slight unusual change, do take a cancer consultation online as a precaution.

Normal Sorts of Cancerin Youngsters:

Dissimilar to diseases in grown-ups, youth cancer is not a consequence of the way of life or natural gamble factors. In uncommon circumstances, adolescent cancer is brought about by hereditary transformations that are acquired from the guardians. The kinds of tumours a youngster will create are not quite the same as grown-up cancer. A portion of the normal youth tumours are:

Leukaemia: Leukemia is a disease of the platelets and bone marrow. It is the most normal sort of life as a youngster cancer, and as per the American Disease Society, it represents around 28% of all youth tumours. Intense lymphoblastic leukaemia (ALL) and intense myeloid leukaemia (AML) are the two essential sorts of leukaemia.

Cerebrum and Spinal Line Growths: Mind and spinal string cancers are the second most normal kind of life as a youngster disease, representing around 26% of all youth tumours. These growths can be harmless (non-carcinogenic) or threatening (destructive) and can influence a youngster’s mental capabilities. As soon as cancer is detected, one can consult a good cancer consultant for advice.

Neuroblastoma: Neuroblastoma is a disease that beginnings in youthful nerve cells and influences youngsters under the age of 10. It can happen in any place in the body however it for the most part begins in the midsection. It is the third most normal sort of young life disease, representing around 6% of all youth cancer.

Wilms Growth: Wilms cancer is a disease of the kidneys (likewise called nephroblastoma) and is most generally tracked down in youngsters younger than 5. It is the fourth most normal sort of experience growing up with malignant growth, representing around 5% of all youth diseases.

Lymphoma: It is a cancer of resistant cells called lymphocytes. It as a rule begins in lymph hubs and can likewise influence the bone marrow and different organs. Hodgkin lymphoma and non-Hodgkin lymphoma are the two fundamental classes of lymphoma.

Rhabdomyosarcoma: Rhabdomyosarcoma is a disease that creates in the delicate tissues of the body, like muscles or connective tissue. It is most generally tracked down in the space of the head and neck, crotch, midsection, pelvis, or hands and legs.

Retinoblastoma: Retinoblastoma is a cancer that creates in the retina, the piece of the eye that detects light and gives vision. It is most regularly tracked down in youngsters younger than 5.

Bone Tumors: Bone cancer ordinarily start in the bones and frequently influence more seasoned youngsters and adolescents. The two principal kinds of bone cancer that happen in youngsters are Osteosarcoma and Ewing’s sarcoma.

While youth diseases are uncommon, they can fundamentally affect a kid’s well-being and prosperity. Their folks really should know about the signs and side effects of different youth diseases and look for clinical consideration assuming they notice any. Early findings and treatment can work on the possibilities of a fruitful result and limit the drawn-out impacts of treatment.

Analysis of Life as a Youngster Tumors:

The analysis of life as youngster tumours and grown-up cancer likewise vary that’s why cancer consultation is important. Youth tumours are much of the time analyzed through a blend of actual tests, blood tests, and imaging tests, for example, X-beams, CT sweeps, and X-ray filters.

[lakshman4]

Pediatric Oncology in Hyderabad

Introduction : 

Pediatric oncology is a branch of medicine that focuses on the  treatment of cancer in children. It is a highly specialized field that requires trained doctors to treat your children and make them comfortable for treatment. The goal of pediatric oncology is to provide the best possible treatment for children with cancer.

Types of cancers in childhood

Leukemia

Lymphoma

Rhabdomyosarcoma

Retinoblastoma

Bone cancer

Brain and spinal cord tumors

Neuroblastoma

Wilms tumor

Common signs of cancer in children 

Most of the symptoms are not identified because they are normal illnesses and injuries in childhood. When the illnesses and injuries are not healing it is better to check with the best pediatric oncologist.

The most common signs are

Pain in some area of body that does not go away

frequent headaches

Sudden changes in vision

Paleness 

Loss of energy

Limping 

Fever and illness that does not go away

Sudden loss of weight 

Treatment for Pediatric Cancers in Hyderabad

The treatment for childhood cancer is not like adult cancer. Pediatric Oncology in Hyderabad is specialty focused care for children suffering from cancer. They make your children feel better while doing treatment. It is very important to choose Pediatric Oncologist in Hyderabad to treat your children 

Chemotherapy is commonly used for children's cancer treatment. They recover faster than adults do when high doses of chemotherapy are applied. If radiation therapy is used for treating childhood cancer children face many side effects than adults. 

Conclusion : When your children are suffering from childhood cancer it is better to consult a pediatrician. In hyderabad we kaizen oncology network having the best Pediatric Oncology Specialist in Hyderabad with experienced and best care for your children and make them comfortable while treatment. Contact us today for the best treatment for your children with cancer.

[drnandinihazarika]

Pediatric Bone Tumors in Delhi NCR

The Best Doctor for Pediatric Bone Tumors Treatment in Delhi NCR

When it comes to the health of our children, finding the right doctor is of utmost importance. Pediatric bone tumors in Delhi NCR are a concerning medical condition that requires specialized care and expertise, One name stands out as a beacon of excellence in the field of pediatric bone tumors treatment – Dr. Nandini Hazarika. With her extensive knowledge, compassionate approach, and remarkable success rate, Dr. Hazarika has earned the reputation of being the best doctor for pediatric bone tumors treatment in Delhi.

Unmatched Expertise:

Dr. Nandini Hazarika is a highly skilled and experienced pediatric orthopedic surgeon specializing in the treatment of bone tumors in children. With years of rigorous training and clinical experience, she has acquired in-depth knowledge in the field. Her expertise extends to diagnosing and managing a wide range of pediatric bone tumors, including osteosarcoma, Ewing's sarcoma, and rhabdomyosarcoma, among others. Dr. Hazarika stays updated with the latest advancements in treatment modalities and employs cutting-edge techniques to ensure the best possible outcomes for her young patients.

Comprehensive Approach:

What sets Dr. Nandini Hazarika apart is her holistic and patient-centric approach to pediatric bone tumors treatment in Delhi. She understands the physical and emotional toll that such a diagnosis can have on both the child and their family. Dr. Hazarika takes the time to listen to her patients and their parents, addressing their concerns and providing them with all the necessary information about the treatment options available.

She believes in a multidisciplinary approach to care and collaborates closely with a team of experts, including pediatric oncologists, radiologists, and pathologists, to formulate personalized treatment plans for each child. Dr. Nandini Hazarika ensures that every step of the treatment journey is well-coordinated, providing comprehensive care from diagnosis to post-treatment follow-up.

Compassion and Support:

Dr. Nandini Hazarika's dedication to her patients extends beyond her medical expertise. She offers a compassionate and supportive environment to children and their families, helping them navigate the challenges that come with a diagnosis of pediatric bone tumors in Delhi. Her empathetic nature and positive demeanor create a sense of trust and confidence, allowing her young patients to feel comfortable and cared for throughout their treatment.

State-of-the-Art Facilities:

Dr. Nandini Hazarika practices at a leading medical facility in Delhi NCR equipped with state-of-the-art infrastructure and advanced diagnostic and surgical tools. This enables her to provide the highest quality of care and perform complex procedures with precision and efficiency. The facility maintains strict hygiene protocols, ensuring a safe and sterile environment for pediatric patients.

Conclusion:

When it comes to the delicate and critical task of treating pediatric bone tumors, Dr. Nandini Hazarika stands out as the best bone tumors doctor in Delhi NCR. Her unmatched expertise, comprehensive approach, compassion, and state-of-the-art facilities make her the go-to specialist for parents seeking the best possible care for their children. Under Dr. Hazarika's guidance, families can find solace knowing that their child's health is in the hands of a dedicated and highly skilled professional.

[toostarlightkitty]

Vaginal Cancer: Symptoms And Causes

Vaginal cancer is a rare form of cancer that develops in the muscle tube connecting the uterus to the outer genitalia, or vagina. The vagina, also known as the birth canal, is lined with cells, and these cells are where vaginal cancer most frequently develops. The likelihood of a cure is highest when vaginal cancer is discovered in its early stages. The treatment for vaginal cancer that has spread outside of the vagina is substantially more challenging. We will discuss vaginal cancer treatment and causes in this blog and all it's challenges.

Types of Vaginal Cancer

Vaginal cancer comes in various forms. The following are the common vaginal cancers:

Squamous Cell Carcinoma

The flat cells, or squamous cells, that line the vagina are where squamous cell cancer originates. The most typical kind of vaginal cancer issquamous cell carcinoma. It represents around 90% of all instances.

Adenocarcinoma

This type of vaginal cancer is found originally in the gland cells of the vagina and commonly affects the younger age group. There is a special variety of vaginal cancer, clear-cell adenocarcinoma. This happens in women who were exposed to a medication diethylstilbestrol (DES) while they were still within their mother’s womb. Paradoxically, this was a medicine used to treat miscarriages till late 1970s. Now it is banned.

Melanoma

It usually starts within the cells that provide colour to the skin neighbouring vagina (melanocytes). Vaginal melanomas are very rare.

Sarcoma

It develops within the connective tissue and muscle tissue that make up the vaginal wall. Vaginal sarcomas are uncommon, just as are vaginal melanomas. Sarcomas come in a variety of forms. The most frequent type is rhabdomyosarcoma, which primarily affects children. While leiomyosarcoma is a disease of middle-aged women.

How Common is Vaginal Cancer?

True vaginal cancers are rare. Vaginal cancer makes up about 2-3% of all gynaecological cancers. Vagina is commonly affected with cancer from other neighbouring organs. These are not primary vaginal cancers.

Who Develops Vaginal Cancer?

The risk of developing vaginal cancer rises if:

The woman is over 60 years old.

If the women develops persistent human papillomavirus (HPV). These infections does not give symptoms.

The individual is diagnosed with vaginal intraepithelial neoplasia (VAIN).

The individual has experienced cervical dysplasia or malignancy.

Women who came into contact with diethylstilbestrol (DES).

Women with smoking habits.

Symptoms of Vaginal Cancer

Early vaginal cancer may not show any symptoms at all. Vaginal cancer may manifest as the following signs and symptoms as it progresses:

Unusual bleeding from the vagina.

Watery or unpleasant vaginal discharge.

Pain in the pelvis.

Pain during sexual activity.

Difficulty in urinating.

Feeling the need to urinate while having an empty stomach.

More urination than usual.

Constipation.

A lump in the vagina.

Cause Of Vaginal Cancer

What specifically causes vaginal cancer is unknown to researchers. Vaginal cancer and high-risk HPV strains are likely linked, just as they are with cervical cancer. It is considered HPV vaccines will also protect against vaginal cancers.

Transmission Of Vaginal Cancer

Cancer cells in the vagina behave like all cancer cells. As the cells grow in uncontrollable fashion, tumours develop. These tumours may invade adjacent healthy tissue and metastasize (spread to other parts of your body).

Diagnosis and Treatment

The following tests and procedures are used for the diagnosis of vaginal cancer:

Pelvic exam

The healthcare professional will visually examine the vulva and feel for any anomalies by inserting two fingers within the vagina. The vagina is spacious. Sometimes the two walls can be temporarily gently separated using a device known as a speculum, making it simpler to see the cervix and vaginal canal.

Pap Smear

The healthcare professional will scrape cells from the cervix while holding the vagina open with a speculum and a spatula-like tool. For indications of malignancy or HPV, these cells will be examined in a lab. It takes a few seconds to take smear.

Colposcopy

The doctor will examine the vagina and cervix using lighted equipment called a colposcope or vaginoscope to check for abnormal cells.

Biopsy

It is frequently performed by colposcopy. In order to check for cancer cells, the healthcare professional will collect a pinch of tissue sample. With friendly advanced local anaesthesia, it is painless. The treatment is determined by the type of cancer, the stage of the cancer, and the patient's age. Precancerous cells are typically treated with removal, laser surgery and topical therapies. Surgery, radiation, and chemotherapy are frequently needed to treat invasive vaginal cancer. There are several therapies that you might get.

Surgery

Wide local excision

The tumour and some of the surrounding healthy tissue are removed.

Vaginectomy (Partial or Radical)

Depending on the size and location of the tumour, the doctor may remove all or some parts of the vagina. The doctor may advise having the lymph nodes, uterus, and cervix removed (lymph node dissection), depending on how far the cancer has spread (hysterectomy).

Pelvic Exenteration

This is needed in advanced cases. This procedure removes several organs, including the bladder, uterus, cervix, vagina, ovaries, and adjacent lymph nodes from the pelvis. The gynaecologic oncologists in saltlake, Kolkata will create an opening in the abdomen for urination and bowel movement (called a stoma or ostomy bag). This surgery is recommended if someone has cancer that keeps coming back.

Radiation Therapy

Radiation kills cancer cells or prevents them from proliferating by using focused energy beams, like X-rays.

External Radiation Therapy

High-energy radiation beams are focused on the tumour by an external machine.

Internal Radiation Therapy

Radioactive materials are inserted into or close to the tumour in the vagina using catheters or sealed wires. These give short doses of radiation and are removed after each dose.

Chemotherapy

In this, cancer cells are killed using medications.

Clinical Trials

World is advancing quick to find novel cancer treatment. Without the help of patients this cannot be achieved. The doctor might offer the patient to enrol in a clinical study to check out innovative cancer treatments.

[drmohsineazam]

What Is Osteosarcoma? What Kinds of Symptoms Does It Cause?

Osteosarcoma is a type of bone cancer that can occur in people of any age. But it is generally more commonly found in adolescents and young adults who are starting to go through puberty. It’s not usually diagnosed until after the patient has already developed symptoms.

What causes osteosarcoma?

Some rare types of cancers cause bone breaks, or osteosarcomas. This makes up about 2% of all cancer diagnoses each year.[1] The major risk factors for this type of cancer are being exposed to high levels of radiation, having a family history of osteosarcoma, and having endocrine-disrupting hormones (like some birth control pills) taken by patients with osteosarcoma. If you are at a higher risk of developing osteosarcoma than others, there may be several warning signs you should watch out for before the disease becomes worse. Treatment involves changing your lifestyle and getting regular checkups with a doctor.

How do I tell if my child has osteosarcoma? One of the first signs a child may have osteosarcoma is a broken arm, leg, or hip. Your child may also complain about pain in his or her jaw or bone in his legs. Children who have these symptoms often receive an “open surgery.

What is the average survival time for children with osteosarcoma?

The survival time for children with osteosarcoma is only 20 months, compared with around two years for those without disease, according to Jain Dhanalakshmi MD, author of 'Osteosarcoma in Young Adults'. For this reason, doctors sometimes call osteosarcomas "young adult disease." There is also little information available about how long children with osteosarcoma will live. However, when treatment is given, it usually lasts from 5 to 10 years, depending on the stage and type of treatment. A recent study found the median overall survival was 10 years in children treated successfully.[2]

What types does osteosarcoma affect?

Osteosarcomas affect bone and soft tissue. They include both primary (involving the whole bone) and secondary (involving one section of the bone) lesions. Secondary lesions are usually found later in life, and are most frequently observed in older adults. These include fractures caused by a fall or sports injury. Primary lesions, however, usually involve only one part of the bone (such as a femur), but they can occur anywhere in the body, including in your spine. Other examples of primary tumors that can form in the spine include rhabdomyosarcoma, chondrosarcoma, osseous angiosarcoma, and chondroglioma.[citation needed] According to the National Cancer Institute, osteosarcoma occurs at five times more frequently in females than males, and it can appear in various forms, including primary or metastatic. The age group most likely to develop osteosarcoma includes teenagers and young adults and includes individuals who are overweight or obese. Most cases also occur during adolescence, and childhood is rarely associated with the development of osteosarcoma. Secondary bone cancers caused by osteosarcomas, such as osteoblastic sarcoma and osteoblastic hyperplasia, represent only 8% to 18% of the total number of new cancers in adults. [3] People with osteosarcoma are at increased risk of contracting certain types of leukemia, multiple myeloma, and other cancers. An increase in the incidence of osteosarcomas over the past decade has been attributed in part to the increasing age of menarche. In fact, women are now at increased risk of osteosarcoma than men. And because osteosarcoma tends to occur earlier in the growth spurt in girls compared with boys, early diagnosis becomes a key component to managing its impact on the overall health of these teenagers.

What symptoms does osteosarcoma cause?

There are three main features to look for in teenagers and young adults who have osteosarcoma. First, they often complain about pain. Second, if they have a fracture, pain is accompanied by bruising and swelling, often accompanied by fever. Third, this might not get better in a few weeks. Sometimes, the patients will start complaining about unusual weight loss. This can be followed by sudden death within days. Also, in older patients, bone metastases are observed. Osteosarcoma can progress over time to lead to massive destruction of bone or even to cause bone cancer. As a result, you should contact our medical team right away if you notice something out of the ordinary.

What kind of drugs can help with osteosarcoma?

Chemotherapy is still used to treat cancer-related bone disorders. While chemotherapy may not entirely cure osteosarcoma, it helps manage the progression and increases survival rates. Unfortunately, this is usually not possible for every patient. Therefore, while surgery may not completely solve your child's problem, proper medical care and good nutrition can help ensure your child remains healthy long enough for surgery. Since chemotherapy cannot target what causes the disease, it is important to consider the possibility that chemotherapy is contributing to the formation of more cancer cells. If so, you should stop taking this drug and discuss surgery with your insurance provider. Another option is hormone therapy, which improves the production of thyroid hormones. Hormones like estrogen help regulate the bones and muscles so they don't become brittle or calcified; hence, they're useful in preventing osteosarcoma. You might also want to try using a topical corticosteroid for painful and tender areas like the thighs and pelvis. Corticosteroids are relatively safe. Unlike chemotherapy, topical corticosteroids tend to be safer because they don't affect the immune system as much as chemotherapy does. If this doesn't work, you can use radioactive iodine for additional protection against bone damage.

What happens after surgery?

Surgery is one way to combat osteosarcoma. After surgery to remove the tumor, your baby will experience many healing processes that will leave him or her feeling normal again. Depending on the type of the tumor, the recovery period can range from a few days to approximately 6 months to a year. Recovery time may depend on the size of the tumor and the general health of the patient. To reduce postoperative pain, your partner can administer narcotic drugs to help relieve pain by blocking receptors that may be involved in inflammation. For some patients, pain relievers given in small doses may be helpful. In addition, depending on how severe your osteosarcoma symptoms are, you may need to take medications to control pain before returning home. Medications include aspirin, acetaminophen, ibuprofen, and naproxen.

What does surgery mean?

Surgeries can treat various problems, including cancers of the heart and lungs. Any operation will require anesthesia, which can be provided by local or general anesthetic agents. Anesthesia can also be administered via intravenous (IV) lines with oxygen support. Because surgery involves removing part or all of the body, it's best to speak with your surgeon about all the potential consequences and talk to them in advance about whether you want to proceed with undergoing surgery. Before surgical procedures, it's advisable to check your blood pressure. Many patients report improved mental status and reduction of anxiety symptoms after an anesthesia procedure. However, if you experience vomiting or excessive bleeding after surgery, seek emergency medical attention immediately. Also, you should monitor your skin color and the amount of fluid in your body. The last thing you want to worry about when you get back home is sagging skin. Make sure to drink lots of fluids and eat a balanced diet. For most patients, minor surgery is typically able to be reversed after a couple of days, whereas complicated or advanced complications require a longer term of follow-up care. For example, surgery is often recommended for patients with conditions like diabetes. Doctors also perform surgeries regularly to stabilize joints or restore movement after injuries such as strokes. A large variety of options are available for treating osteosarcoma. Whether this process can successfully be reversed depends on how well you handle postoperative side effects. Pain management is another concern for patients with osteosarcoma. If your surgery involves incision, pain medication, or anti-inflammatory drugs, make sure you don't experience postoperative discomfort. When you return home following surgery, you'll want to keep yourself hydrated. Excessive thirst is usually the result of dehydration rather than decreased electrolytes in the body. Drinking plenty of fresh water can help replenish lost minerals after surgery, so be careful about drinking. Finally, it's important to remember that although your body will recover immediately following surgery, you may not feel as completely healed immediately. Some pain medication will take some time to pass into your bloodstream. Always continue to take pain relief medications, especially when you notice increased signs of joint pain.

What are the treatment and prognosis for osteosarcoma?

Once your child is stable, you should discuss the treatment plan with your healthcare provider. Usually, surgery is a safe, effective, and reliable option for treating osteosarcoma. At least half of all patients in the United States have had their tumor successfully removed in the early stages, usually within 1 year. However, surgeons may recommend different treatments, depending on the location of the tumor and overall health of the patient. For example, some children are good candidates for radiotherapy or cry

Conclusion

Osteosarcoma is a type of bone cancer that can occur in people of any age, but is most common in teenagers and young adults. It is a very aggressive form of cancer that can spread quickly to other parts of the body. Symptoms of osteosarcoma include pain in the affected bone, swelling, and fatigue. If you experience any of these symptoms, it's important to see a doctor right away so that you can begin treatment as soon as possible.

[rinkrats]

At age two, Dian Green was diagnosed with rhabdomyosarcoma, a rare type of cancer, and was treated with chemotherapy and radiation. At six, he was diagnosed with acute lymphoblastic leukemia. His younger brother was a match for a bone marrow transplant which was successful.

This past November, he was diagnosed with osteosarcoma, a type of bone cancer, and has been in treatment since then.

"Through Dream Factory, we were told that Dian could have a wish and his wish was always to meet Sidney Crosby," she said.

Dian, whose middle name is Sidney, had asked his mom to bead him a Penguins logo medallion prior to knowing about the meeting with Crosby.

Then on April 14, the Pittsburgh Penguins player took Dian through an on-ice, half hour tour via an online video conference similar to FaceTime.

"We kept the news from him until the morning of the interview," his mom said. "We told Dian that it was about to happen and we just wanted to keep it a big surprise. And he was just so amazed, like he couldn't believe that it was going to happen. He was so nervous, so shy."

During the meeting, Dian wore his medallion proudly and Crosby asked him about it.

After the meeting was over, Dian asked his mom if they could make the three-time Stanley Cup Winner a similar medallion and send it to him as soon as it was completed.

"Just to see my son's hockey idol wearing a medallion that matches my son's medallion that I beaded, it's something to be very proud of," said Rachel, Dian’s mother.

-Child battling cancer fulfils dream of meeting Sidney Crosby, gives him beaded medallion, 30 April 2021

[rhythmicgymnasticsnews]

Unfortunately, Valeriia Yuzviak has been diagnosed with rhabdomyosarcoma. She has a good chance of recovery, fortunately, but she needs to raise money in order to get treated at a clinic in Germany. The Ukrainian Federation will pay for some part of her costs, but she still needs help to obtain the rest of the sum.  

(You can find her account details below, but also check her Instagram stories or the Instagram page of the Ukrainian Federation for information)

5363542015389795 UAH

5363542015389787 EUR

Юзьвяк Валерія Вадимівна

Yuzviak Valeriya

Bank Name: Privatbank

Account Holder Name: Yuzvjak Valeryja

IBAN: UA633052990000026202898581190

SWIFT Code: PBANUA2X

Adress: UKRAINE, Kyiv, 1D Hrushevskoho str.⠀

For any additional questions regarding the financial support of our gymnast, please contact the Ukrainian Gymnastics Federation in Instagram: @ukr.gym.federation.

[thewrongjackpot]

I hit the wrong jackpot. *Spoiler alert, it’s cancer.*

[Originally written 1/3/20]

Warning: There may be a fair amount of sarcasm throughout this post coupled with some dark humor. Also, if you’re new to this channel, please disregard a lot of the other ramblings here, unless one dares to be bored.

“What jackpot did you hit?” you may ask. I hit the cancer jackpot. You read that right. C-A-N-C-E-R. This fun-loving 26-year-old has been diagnosed with Rhabdomyosarcoma and of a newer subtype called Sclerosing. Take those words in. I had to have Google repeatedly tell me how to say it before I got the hang of it. It’s a jackpot because to say it is uncommon in adults is an understatement. A friend told me I need to get my butt to Vegas with all this rare luck.

“Wait, what? How did this all happen?” asked no one. Here’s a fun “little” deep-dive into everything that’s been going on the past few months, and how I’ve been dealing with it. Remember, you chose to continue reading this long post from here on out.

Well, let’s take it back to early-mid August. It started with what I thought was just TMJ issues because I was stressing some and clenching my teeth, so my jaw and temple started off sore. It then progressed to limited range of motion with my jaw (opening/closing), a small protrusion along my temple, and some numbness on my face. The urgent care doc essentially told me it’s TMD, the muscle is swollen, to chill, and it’ll go away. Well, that was extremely off. I saw my primary doctor, who then referred me to an ear, nose, and throat (ENT) doctor. Now, we’re at the end of November, and I had to take some MRIs and then was referred to another ENT doctor. I had a biopsy, and the doctor said it looks more mild-moderate than severe like he was initially thinking, but he was pretty sure it was malignant with how quickly it has been growing. Christmas Eve morning, I get a phone call. The final pathology came about, and it’s an intermediate grade Rhabdomyosarcoma. I was referred to a hospital with a Sarcoma specialist and saw her just after the new year began. She doesn’t know staging yet because she doesn’t know if it has spread anywhere else yet. I only had MRIs done and that was over a month ago now. So next week I get the joyous pleasure of more MRIs, a bone scan, a lumbar puncture, and a bone marrow biopsy. EXCITING. They’re also going to need to start chemo soon, so they’re working on getting that set up in the background. As of right now, the oncologist was saying it’ll be about 5 months of chemo, radiation and/or surgery, and then more chemo. More will be known in the coming weeks, but at least there’s finally a real start and direction to this all.

Needless to say, it’s been a crappy holiday season and last several months.  Here’s a list of what this jolly (not green) giant growth in my head/neck has caused:

Swollen temple/face

Limited ability to open my mouth (~1.5cm)

Misaligned jaw

Numbness along half my face

Sharp shooting pains throughout my head/neck

Impacted breathing out of my left nostril

Fluid in my left ear (impacted hearing)

Trouble swallowing

Fatigue

Body aches

Pressure throughout the entire left side of my head

Large growth(s) inside my mouth encompassing cheek/mouth real estate

Accidentally chewing on said growths, which I think is the reason there’s blood in my mouth periodically

After my first meeting with the oncologist the other day, some topics hit home harder than others.

One of the points that almost made me cry on the spot was when I was asking about fertility. She was saying that she could recommend me to a fertility clinic to harvest my eggs. However, that could take 2-4 weeks, and we might not have that time to spare. I know that there’s so much more at stake, my health and well-being  taking spot numero uno. I also know that there are other ways to still have kids, but it’s still such a depressing feeling and thought. Along with hearing that 2-4 weeks is not time that can be spared, it begs the question, “How bad/serious is this really?”. Having my own child is a choice that may never even be mine to begin with.  I just always had this picture in mind about how life would be never thinking this is the luck I would be dealt. Then again, I don’t think anyone ever envisions something like this happening to them… Although, my vision of six dogs at any given time could become more of a reality. *shrug* (Honorable mention goes out to my brother who was cheering me up big time on this one.)

Next, the fear started to really set in when talking about all these tests that needed to be done. I’m absolutely terrified of pain, and the thought of all these huge needles makes me want to cry, throw up, and pass out. It’s not just the pain and needles I’m afraid of, it’s everything that comes along with the actualization of what this really is. Since we don’t know the full extent of this, my mind can’t help but think the prognosis is possibly more grim with all these tests needed and how quickly this tumor has dominated my face. I’m scared about having to go to treatments, having to feel sick, fatigue setting in, and withering away. I’m scared about losing my hair because, boy, let me tell you, I’ve always had long thick hair my whole life. There are only two occasions I can think of where my hair was shorter than mid-back. I’ve broken down crying several times in the shower while washing my hair; it was always a safety blanket for me. Although, I said I should jump the gun and get a bowl cut already haha. On a more serious note, I’m absolutely mortified that I’m not going to make it through this…but being a fighter and a survivor is in my blood, so I’m trying to not let that run my mind too much.

On a more physical and literal level, one of the most debilitating aspects of this is the limited range of motion with my mouth because I can barely eat. Eating has become almost a punishment because after a few bites of something, it hurts everywhere. It’s hard to swallow at times; it’s just all-around depressing. At this point, I’m closing in on having lost 30 pounds in about three months. I’m eating maybe 1000 calories a day. I try to force myself to eat, but it’s difficult. Some days everything makes me nauseous. I’ve mostly been drinking smoothies, eating soup, and other soft foods like mashed potatoes. Even when I am eating something, it’s extremely defeating when I wipe soup off my chin because the little piece of potato couldn’t fit in my dumb mouth and caused soup to drip down, and I couldn’t feel it because my face is too busy being numb. Moments like that are extremely disheartening. Stupid mouth.

Also, another difficult aspect of this is sleeping. I haven’t gotten a good night’s sleep in months. No matter which way I lie, there is either uncomfortable pressure or some sort of pain. I’ve literally woke up crying like a fussy baby because it hurts so much, and all I want to do is sleep.

DESPITE ALL OF THIS, I’m down, but I’m not out. I still have so many things to be grateful for. My husband continues to be amazingly strong, knows how to comfort me when I need it, and has been picking up my slack. Some of my family members have seriously stepped up in ways I could not have imagined that genuinely caught me by surprise. For those family members who have been with me on this so far, they have been so supportive and simply there for me when I need them. My parents are doing whatever they can from wherever they are to help me, e.g. my mom is flying up next week to be with me. I have some solid friends, and even my husband’s friends have been amazing. Work is working well with me through this, and even my old boss and coworkers have been checking up on me. Side note: I saw this lady at work today (whom I rarely interact with) only to find out her brother got treated where I am by the same set of doctors, and she said his experience was great as was the staff. That was an unexpected nugget of good vibes I did not expect today or ever.

One of the other biggest items I realized a few days ago that I am extremely grateful for is having moved away from Hawaii. Since moving, I go back and forth on whether leaving was the best decision, but now who knows what would be of me if I didn’t. If developing this cancer was an inevitable piece of my life story, being in Hawaii would have been one of the worst things for me. For one, there are doctor shortages, so being seen would have been dragged out so much longer than here. Secondly, Hawaii does not have the specialists to even treat me. I would have had to fly somewhere else anyway. As an aside to this, I’m even more grateful that we moved to the west coast because family is more accessible than in DC, and my husband and I have friends here as well.

Well, that’s about it for now. I like to talk/write, so I’m honestly going to post updates on here even if they fall on deaf ears. Just like this page says, I’m someone rambling lol.

If you’ve made it this far, I’ll give you a cake pop one day or something.

TL;DR

I have a rare form of cancer that’s been progressing pretty quickly. A lot of it really sucks right now, but there’s finally some real direction in getting me treated. Also, I am surrounded by a lot of love and dope people, and I still have so much to be grateful for.

[drpurvikadakiakutty]

 Dr. Purvi Kadakia Kutty: Leading Child Oncologist in Navi Mumbai with Over 11 Years of Experience    

Dr. Purvi Kadakia Kutty stands as a beacon of hope and expertise in the field of pediatric oncology in Navi Mumbai. With an illustrious career dedicated to the treatment and care of children battling cancer, Dr. Kutty has garnered a reputation for her compassionate approach, clinical excellence, and unwavering commitment to advancing pediatric cancer care.

Child Oncologist  in navi mumbai encompass a range of malignancies affecting children and adolescents. These cancers differ from those found in adults both in terms of their types and how they respond to treatment. Some common types include:

Leukemias: These are cancers of the bone marrow and blood and account for about 30% of childhood cancers. The most common types are acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML).

Brain and Central Nervous System (CNS) Tumors: These tumors develop in the brain or spinal cord and are the most common solid tumors in children. They vary widely in type and location, affecting different parts of the CNS.

Neuroblastoma: This cancer develops from immature nerve cells and often starts in the adrenal glands but can also occur in nerve tissue along the spine, chest, abdomen, or pelvis.

Wilms Tumor: A type of kidney cancer that primarily affects children, usually diagnosed around age 3 or 4. It typically responds well to treatment.

Lymphomas: These cancers start in the lymphatic system and can be either Hodgkin lymphoma or non-Hodgkin lymphoma. They can occur in children, although they are more common in adolescents.

Rhabdomyosarcoma: A type of soft tissue sarcoma that forms in muscle tissue. It can occur anywhere in the body but often begins in the head and neck area, urinary and reproductive organs, arms, or legs.

Retinoblastoma: This is a rare cancer of the eye that usually occurs in children under the age of 5. It develops in the retina, the light-sensitive layer of cells at the back of the eye.

Each type of childhood cancer presents unique challenges in terms of diagnosis, treatment, and long-term management. Advances in research and treatment have improved outcomes significantly over the years, with many childhood cancers now having high survival rates when diagnosed early and treated appropriately.

Dr. Purvi Kadakia Kutty is a distinguished pediatric Child Oncologist dedicated to treating and researching childhood cancers. With an unwavering commitment to her young patients and their families, Dr. Kadakia Kutty brings a compassionate and comprehensive approach to her practice. She specializes in diagnosing and treating various pediatric cancers, including leukemia, lymphoma, and solid tumors, employing the latest advancements in medical technology and treatment protocols.

Dr. Kutty's expertise encompasses Child Oncologist  in navi mumbai a wide range of pediatric cancers, including leukemias, lymphomas, brain tumors, and solid tumors. She is well-versed in the latest treatment protocols and is adept at employing a multidisciplinary approach to cancer care, involving surgery, chemotherapy, radiation therapy, and targeted therapies. Her ability to tailor treatment plans to the unique needs of each child has made her a trusted and sought-after oncologist in Kharghar, Navi Mumbai.

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.

In addition to her clinical practice, Dr. Kutty is actively involved in pediatric oncology research.Kharghar, Navi Mumbai  She has contributed to numerous studies aimed at understanding the underlying mechanisms of childhood cancers and developing innovative treatment strategies. Her research work has been published in several reputable medical journals, reflecting her commitment to advancing the field and improving outcomes for children with cancer.

Visit: https://childoncologist.com/ 

Contact: +91 77381 62020

[enzaime-blog]

Nate’s Soft Tissue Sarcoma Story

New Story has been published on https://enzaime.com/nates-soft-tissue-sarcoma-story/

Nate’s Soft Tissue Sarcoma Story

Nate’s parents noticed a large lump on their five-year-old son’s left calf during bath time. Their pediatrician ordered tests revealing alveolar rhabdomyosarcoma – a type of tumor that affects muscle tissue – which had already spread to the lymph nodes. Several specialists said that amputation was the only option. The family came to Memorial Sloan Kettering, where Nate underwent intensive treatment to save his leg – and his life.

It all started on a beautiful Sunday afternoon in April 2004. Nate’s parents, Aliza and Ben Goldstein, had taken Nate, his brother, Ryan, and his sister, Abigail, to a nearby empty parking lot, where Abigail was learning how to ride a two-wheel bike. The bicycle lesson was followed by a trip to the ice cream shop, a perfect ending to a seemingly average, ordinary day.

When they returned home later that evening, all the kids went straight to the bathroom to be bathed. During the bath, Aliza noticed a very large lump covering Nate’s entire left calf. Concerned about the suspicious mass, Aliza took Nate to see her cardiologist father, who lived nearby. “I’ll never forget my father’s words,” Aliza says, remembering back to that fateful evening. “He said: ’You need to call your pediatrician immediately.’”

When she telephoned Nate’s pediatrician and described, with her father’s help, the mass on Nate’s leg, the pediatrician asked that they come directly to his house. “Not a good sign,” Aliza recalls thinking. When they arrived at the doctor’s house, after a quick examination of the suspicious lump, the doctor ordered a CT (computed tomography) scan for that same evening.

“Whose Child Has Cancer!?!”

The results of the CT scan showed that the mass was not a cyst, but further testing was required to see if it was malignant, requiring an MRI (magnetic resonance imaging) scan to be scheduled. Nate’s pediatrician scheduled the test for the next morning at a cancer center near the Goldstein family’s New Jersey home. When Aliza asked the doctor why Nate had to go to a cancer hospital, the doctor reassured her it was probably not cancer. “Everyone was afraid to say the word,” Aliza notes. Though she, too, was unwilling to admit the possibility, even to herself. “I thought at the time, ’Come on, whose child has cancer!?!’”

After the MRI was completed, the Goldsteins received the call that is every parent’s nightmare: Nate had cancer. “My life was destroyed,” Aliza says simply. “Our life as we knew it before finding the lump was now over.” The MRI was quickly followed by a biopsy. The biopsy showed that Nate had a form of sarcoma known as alveolar rhabdomyosarcoma, which is a type of tumor that affects muscle tissue. To make matters, worse, Nate’s tumor was diagnosed as an advanced, aggressive stage IV, which had already spread to the lymph nodes in his abdomen.

One in Four Chance — Unacceptable

Still in shock from the news, the Goldsteins sought medical opinions from two different medical centers, one in Philadelphia and one in New Jersey. Physicians from both centers recommended amputating Nate’s leg from the pelvis down. “They all said, ’We are going to amputate Nate’s leg. We are going to give him chemotherapy and radiation therapy, and even then he will only have a one-in-four chance of surviving,’” Aliza remembers with dismay. “One doctor went so far as to tell us that it was not too late to spend time with our son.”

At this time, one of Ben’s friends and neighbors, a cardiologist whose medical school roommate had done a fellowship at Memorial Sloan Kettering with Leonard Wexler, intervened. He made the Goldsteins promise that they would see Dr. Wexler, a pediatric oncologist specializing in the treatment of bone and soft-tissue sarcomas, for one final opinion.

They met with Dr. Wexler the following Monday. He informed them that he was conducting a clinical trial for rhabdomyosarcoma, which, unlike the standard three-drug chemotherapy regimen, included seven drugs. After examining Nate and reviewing his records, Dr. Wexler stated that the survival statistics they had been given were unacceptable and that he didn’t think Nate’s leg had to be amputated. “He couldn’t promise to change the survival numbers,” Aliza says, “but he was trying to give these kids a better chance at living with his clinical trial.”

The deciding factor for Aliza and Ben came when Dr. Wexler mentioned the late effects Nate would have as an adult as a result of his treatment. “This was the first time anyone had mentioned a future for Nate past the cancer. Dr. Wexler hadn’t written off my son. He had given us hope.”

The Goldsteins decided to go with Dr. Wexler because, with his experience treating rhabdomyosarcoma, they knew they could trust him with treatment decisions that differed from what the other hospitals were recommending. “As parents, you’re not pediatric oncologists,” Aliza notes. “You’ve known about rhabdomyosarcoma for a week! You have to choose a doctor you can trust. Once you do, you have to trust him.”

Grabbing Fun Whenever and Wherever Possible

During the first week following the diagnosis, Aliza was so upset that she was unable to eat or sleep. “At some point,” explains Aliza, “a voice in your head says, ’Cut it out. You have to get focused. Your son’s life depends on it.’ And that’s just what we did.”

 This was the first time anyone had mentioned a future for Nate past the cancer. Dr. Wexler hadn’t written off my son. He had given us hope.

Aliza GoldsteinNate’s Mother

What followed for Nate, starting in May 2004, were 12 rounds of high-dose chemotherapy.

“It was horrendous,” Aliza remembers, likening cancer treatment to a roller coaster ride. “We became very day-focused. If Nate was feeling good one day then we would do something fun that day. Because you don’t know what’s going to happen later that night or the next day. We went from being this very planned type of family to a very in-the-moment type. Any fun we could grab and hold onto to be normal, we did. For example, although we’re Orthodox, when Nate was in the hospital during Christmas, we even celebrated Christmas!”

A Lifetime’s Best News — Remission

In order to kill any remaining tumor cells, Nate received 48 consecutive days of radiation therapy, stretching from August to October 2004. In December, the results from a series of scans showed that some of the tumor cells remained, necessitating the surgical removal of Nate’s left calf muscle. The surgery, performed by pediatric surgeon Michael La Quaglia, was a success, removing the tumor cells and preserving Nate’s leg function.

The Goldstein’s anxiety level was high when they went in for the next round of diagnostic scans in March. “Dr. Wexler, knowing we were nervous wrecks, called us at home in the evening of the day of the scan to tell us Nate’s cancer was in remission,” Aliza says. “It was the best news I had ever received in my life.”

In May 2005, Nate started on maintenance chemotherapy, which he was able to receive at home. And his final day of chemotherapy was completed in October 7, 2005. “On October 8th,” Aliza notes, “we began ’life after cancer.’”

The muscles in Nate’s leg had contracted due to the surgical removal of the calf muscle and the radiation treatments. Michael Stubblefield, a physician in Memorial Sloan Kettering’s Rehabilitation Service, used a technique that involved 12 weeks wearing what is known as a serial cast, which slowly stretched Nate’s leg muscles. The cast was combined with injections of Botox to paralyze his muscles in order to avoid cramping during the stretching process. “Before the procedure, Nate stood on the affected foot’s tip-toe,” Aliza says. “After the procedure and the physical therapy that followed it, he could walk normally again.”

 I was fortunate to work at this institution at a moment when I could offer a family and a little boy with a very serious case of cancer a treatment that was not available elsewhere.

When the Goldsteins look back over the past two devastatingly difficult years and the remarkable outcome, they feel blessed. “We feel that it was Dr. Wexler’s insistence on Nate’s quality of life that gave our child a chance at a normal life,” Aliza says. And as proof, she points to an event from this past summer, when Nate broke a board in half with his left leg at karate school. “That was huge,” Aliza says, smiling at the memory. “Dr. Wexler even came to witness it. Our child was supposed to be dead or at the very least not have a leg, and here he was breaking a board with that same leg. It was so remarkable, everybody in the room was crying.”

[virinchihospitals90]

knee pain specialists in Hyderabad - Virinchi Hospitals

Virinchi Hospitals: Your Trusted Orthopedic and Spinal Care Center in Hyderabad

At Virinchi Hospitals, we understand that the backbone of a healthy life is a healthy spine. The numerous causes of back pain can often make life challenging. With our tag as the best hospital for back pain in Hyderabad, we are committed to providing personalized and advanced treatments for each patient.

Specialized Spinal Surgery Procedures Include:

Disc Surgery

Advanced Microsurgery for disc ailments

Fixation systems specially designed for fractures

Surgical correction of spinal deformities

Cutting-edge procedures for spinal tuberculosis

State-of-the-art endoscopic spine surgery

Holistic Arthritis Care: From Osteoarthritis and Rheumatoid arthritis to the less common Infective and Traumatic arthritis, our comprehensive care ensures patients lead a pain-free life.

Pediatric Orthopedics: Children have unique bone structures and issues. Our specialized services include treatments for:

Osteotomies for conditions like Knock knees and bowlegs

CTEV

Hip Dysplasia

Advanced fracture management with flexible nails

General Orthopedic Care at Virinchi Hospitals:

Comprehensive fracture and trauma care

Specialized hand and shoulder surgeries

Cutting-edge micro vascular procedures including nerve repair, and nerve and muscle grafts

Expert care for foot and ankle injuries

Best-in-class treatment for sports injuries and limb deformities

Pioneer in tumor surgeries for bone cancers such as osteosarcoma, Ewing’s sarcoma, chondrosarcoma, and soft tissue sarcomas like rhabdomyosarcoma.

Being recognized as the best orthopedic hospital in Hyderabad isn't just an honor; it's a testament to our unwavering commitment to excellence in patient care. And with the added reputation of performing the best arthroscopic surgery of the knee, we stand unmatched.

Arthroscopic Knee Surgery at Virinchi Hospitals: Our team of internationally trained orthopedic surgeons specializes in arthroscopic treatments. Before any surgical intervention, patients undergo a thorough diagnostic procedure, both conventional and arthroscopic. Post diagnosis, arthroscopic intervention is used to correct the knee condition, with a primary focus on restoring functionality and minimizing pain. Prior to surgery, we ensure patients are educated on the required precautions, surgery preparations, and post-operative care. Additionally, our doctors discuss potential risks associated with the surgery.

Conditions treated through Arthroscopic Surgery include:

Anterior Cruciate Ligament (ACL) tears

Articular cartilage damage

Knee fractures and sepsis

Loose bodies in the knee

Misaligned or dislocated patella/kneecap

Osteoarthritis of the knee

Popliteal cyst and much more

For those searching for the best orthopedic doctor in Hyderabad, the finest knee pain specialist in Hyderabad, or the top orthopedic surgeon in Hyderabad, Virinchi Hospitals is the answer. As the apex of orthopedic care, Virinchi Hospital remains committed to delivering excellence at every step. Your trust in our services drives our dedication.

Address: Virinchi Circle, Rd Number 1, Banjara Hills, Hyderabad, Telangana

Phone.no: 040 46999999

Website: https://virinchihospitals.com/orthopedics/

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[coffeecakeandkegels]

Grief Is A Thief

I lost my best friend at 26 years old. I have lost grandparents I loved dearly and yet their loss did not impact me in the way his death had. I expected my grandparents to die, after all, that is the order in which life is supposed to go.

The day after my 24th Birthday, my friend was diagnosed with Rhabdomyosarcoma, an aggressive sarcoma of the connective tissue and bone. Despite the abysmal prognosis from the oncology intern at our local hospital, Sloan Kettering in NYC treated his cancer aggressively. He was blessed with two more years of life until his cancer came back with a vengeance Jan 7, 2001.

On June 4, 2002 I got the phone call at work that he had passed away. I had been waiting for that phone call and ironically, I was not upset. I held it together. Little did I realize, I held it together by a barely there thread because at the funeral, I lost it. It hit me. I will never hear his voice again. I will never see his smile again. We will never fight over the stupidest, most inconsequential things again. Never again is a permanence we never truly think about. I felt as though I had been robbed in so many ways.

All these years, I thought I managed my grief but I hadn’t. Grief isn’t something to be managed. It’s been 17 years and I still think of him daily and the overwhelming sadness is still the same. It hasn’t gotten better and time does not heal all wounds. The years that followed, I felt an emptiness nothing could fill. That emptiness still exists.

It took me a long time to realize that I never fully grieved. Grief is sly. It tricked me into thinking I had moved past the loss and then out of nowhere, it hits me. When it does, I feel as though I have crashed into that brick wall all over again.

Everyone processes grief differently but I think most can agree with grief leaving them feeling robbed. People often say, “life must go on” and yes, it does. However, we carry our grief with us and it becomes a part of who we are. Words cannot dissolve grief, it impacts every area of our lives and permanently changes us. Grief is a shrewd thief because it steals what we did not know could be stolen. It steals the sparkles that once resided in eyes. It steals the smiles that were once contagious. It steals pieces of hearts, and leaves behind an emptiness that cannot be filled.