24/7 Customer Assistance
24/7 Assistance with the best medical care at your service
Call us for any question
+91 90858 83067Gurgaon,Haryana, India, 122001
IndiaOffice Hour: 09:00am - 09:00pm
info@medigocare.comOriginating in the adrenal glands, located above the kidneys, neuroblastoma is a rare type of cancer that develops in nerve tissue. It occurs particularly in infants and young children. According to studies, approximately 8 children per million under the age of 15 are diagnosed with neuroblastoma. It accounts for 8-10% of all childhood cancers. Neuroblastoma can also occur in areas of the chest, abdomen, near the spine, and neck.
Thank you for reading this post, don't forget to subscribe!This cancer type arises from immature nerve cells called neuroblasts. They normally mature into nerve cells. However, in neuroblastoma, they grow uncontrollably. Neuroblastoma can vary greatly in its behavior. It ranges from slow-growing tumors that may spontaneously regress to aggressive cancers. These cancers spread rapidly to other parts of the body.
Neuroblastoma symptoms may include:
Neuroblastoma diagnosis typically involves imaging tests, such as:
Along with biopsy to confirm the presence of cancerous cells. Neuroblastoma treatment in India depends on the risk group of the patient. The risk group is determined by:
In India, the survival rate of neuroblastoma can vary depending on various factors such as:
● the stage of the cancer at diagnosis,
● the age of the patient, and
● the availability of advanced treatment options.
Generally, the survival rates for neuroblastoma have improved over the years. This is due to advancements in medical technology and treatment approaches. However, the neuroblastoma prognosis can still be challenging. This is especially in cases where the cancer has spread extensively or if it recurs after treatment. The neuroblastoma treatment in Indiatypically involves a combination of:
● surgery,
● chemotherapy,
● radiation therapy, and
● sometimes immunotherapy or targeted therapy.
The success of treatment and the overall prognosis can also be influenced by factors such as:
● the tumor’s location,
● its response to treatment, and
● the patient’s overall health.
It is essential for patients and their families to work closely with a multidisciplinary medical team. This will enable them determine the most appropriate treatment plan. Thereby, patient can receive comprehensive support throughout the treatment process.
Neuroblastoma predominantly affects infants and young children. The exact cause of neuroblastoma is not fully understood. However, researchers have identified several factors that may contribute to its development. Understanding these potential causes can aid in early detection and prevention strategies.
Alterations in chromosomes have been observed in individuals with neuroblastoma. Particularly chromosome 1, chromosome 11, and chromosome 17. These chromosomal abnormalities often affects genes involved in nerve cell development. As a result, these abnormalities contribute to the development of neuroblastoma in children and adults.
In many cases, neuroblastoma is associated with genetic abnormalities or mutations. Certain gene mutations, such as those in the ALK gene or PHOX2B gene, have been linked to an increased risk of neuroblastoma. These genetic changes may disrupt normal cell growth and division, leading to the formation of tumors.
During pregnancy or early childhood, individuals face certain environmental factors. This may increase the risk of neuroblastoma in adults and children. These factors may include:
However, the role of environmental exposures in neuroblastoma development is still being researched.
Neuroblastoma may run in families in small percentage of cases. This suggests a hereditary predisposition to the disease. Children with a family history of neuroblastoma or other cancers may have an increased risk of developing the condition. Genetic testing and counseling may be recommended. This is for families with a history of neuroblastoma. It will help assess the risk of hereditary forms of the disease.
Despite extensive research, the precise cause of neuroblastoma remains unclear. In many cases, it is likely that a combination of:
Further studies are needed to elucidate the complex interplay of these factors. Studies will also help determine their role in neuroblastoma pathogenesis
Neuroblastoma generally originates in nerve tissue. Itcan appear in various forms and locations within the body. Understanding the different neuroblastoma types is crucial for accurate diagnosis and treatment planning. Here are some of the common neuroblastoma types:
Neuroblastoma type confines to its site of origin and doesn’t spread to the other parts of the body. Localized neuroblastoma is often detected early. This type of neuroblastoma has a better prognosis compared to advanced stages of the disease.
This refers to cancer that has spread from its original location to distant sites in the body, such as:
Metastatic neuroblastoma is associated with a poorer prognosis. It requires more aggressive treatment approaches
High-risk neuroblastoma refers to tumors that have aggressive features. They are associated with a high likelihood of recurrence or treatment resistance. These tumors may be characterized by:
● certain genetic mutations,
● extensive spread, or
● other unfavorable factors.
Treatment for high-risk neuroblastoma often involves intensive multimodal therapy. It may require specialized treatments such as immunotherapy or targeted therapy.
Treatment approaches of neuroblastoma in India vary depending on the neuroblastoma stage. It is crucial for accurately assessing the extent of disease and guiding treatment decisions. Here’s a breakdown of the various neuroblastoma stage:
Stage L1 neuroblastoma refers to localized tumors. These tumors are confined to their site of origin. They can be completely removed through surgery. These tumors typically have favorable features and are associated with a high likelihood of cure. The prognosis for patients with stage L1 neuroblastoma is generally excellent, with a high survival rate.
Stage L2 neuroblastoma also consists of localized tumors. Unlike stage L1, these tumors cannot be completely removed through surgery. However, they have not spread beyond their site of origin or nearby lymph nodes. While stage L2 neuroblastoma may require more extensive treatment than stage L1, such as:
● chemotherapy or
● radiation therapy.
The neuroblastoma prognosis is still favorable compared to more advanced stages of the disease.
Stage M neuroblastoma indicates cancer that has metastasized or spread to distant sites in the body, such as the:
● bones,
● bone marrow,
● liver, or
● other organs.
These tumors are often more challenging to treat. They are associated with a poorer prognosis compared to localized neuroblastomas. Treatment for stage M neuroblastoma may involve intensive multimodal therapy, including:
● chemotherapy,
● surgery,
● radiation therapy,
● stem cell transplant,
● immunotherapy, or
● targeted therapy,
depending on the extent of spread and other factors.
Stage MS neuroblastoma refers to tumors that have spread to distant sites in the body but are limited to certain metastatic sites, such as the
● skin,
● liver, or
● bone marrow.
These tumors may be associated with favorable prognostic factors and may respond well to treatment. However, close monitoring and comprehensive treatment are still necessary. This is in order to prevent disease progression and recurrence.
The signs and symptoms of neuroblastoma may vary depending on the location and size of the tumor. The cancer can spread to other parts of the body as well. Some children may not show any symptoms initially, others may experience the following signs and symptoms:
Bone Pain: Neuroblastoma can spread to the bones, particularly the bones of the
● legs,
● pelvis,
● chest, or
● spine,
leading to bone pain or limping. Children may experience
● discomfort,
● tenderness, or
● difficulty bearing weight on the affected limb.
Abdominal Mass or Swelling: One of the most common signs of neuroblastoma in infants and young children is the presence of a:
● firm,
● painless mass or
● swelling in the abdomen.
This mass may be noticeable during routine physical examinations or may cause the abdomen to appear distended.
Changes in Bowel or Bladder Habits: Neuroblastoma tumors in the abdomen may press against nearby structures. This causes changes in bowel or bladder habits. This may include:
● constipation,
● diarrhea,
● difficulty urinating, or
● urinary incontinence.
Fever: Some neuroblastoma in children may develop unexplained fevers. The fevers may be persistent or recurrent. Fever may occur due to the body’s immune response to the cancer or as a result of infection associated with bone marrow suppression.
Fatigue and Weakness: Neuroblastoma can cause:
● general fatigue,
● weakness, and
● lethargy in affected children.
This may be attributed to anemia, nutritional deficiencies, or the body’s response to the presence of cancer.
Proptosis (Eye Bulging): Tumors arising in the chest or abdomen may press against the nerves that control eye movement. This leads to proptosis or bulging of one or both eyes. This may cause a noticeable difference in the appearance of the eyes or vision changes.
Weight Loss: Children with neuroblastoma may experience unexplained weight loss. This can be despite having a normal or increased appetite. Weight loss may occur due to metabolic changes associated with the cancer or as a result of reduced food intake due to abdominal discomfort.
Other Symptoms: Depending on the location of the tumor, children with neuroblastoma may also show symptoms such as:
● respiratory difficulties,
● bone fractures,
● bruising,
● irritability, or
● generalized malaise.
The diagnosis of neuroblastoma involves a comprehensive approach. This may include medical assessments and diagnostic tests. The process begins with a:
● thorough physical examination and
● medical history review by a healthcare provider.
During the physical examination, the healthcare provider may palpate the abdomen. This is to check for the presence of a mass or swelling. He/ she will assess any signs of proptosis (eye bulging). Then, he/ she will evaluate other symptoms or abnormalities that may suggest neuroblastoma. Additionally, obtaining a detailed medical history helps identify any relevant familial predispositions. It will aware the healthcare provider about past medical conditions that may contribute to the diagnosis.
Following the initial evaluation, blood and urine investigations are commonly performed. This helps assess specific markers associated with neuroblastoma. Blood tests may include measuring levels of certain substances, such as:
● catecholamines (e.g., dopamine, norepinephrine), and
● various tumor markers (e.g., neuron-specific enolase, ferritin),
which can be elevated in patients with neuroblastoma. Urine tests may also detect increased levels of catecholamines and their metabolites. This helps in providing valuable diagnostic information.
Imaging tests play a crucial role in confirming the presence of neuroblastoma. It helps in determining the extent of disease spread, and guiding treatment planning. These imaging modalities may include:
● ultrasound,
● computed tomography (CT) or
● magnetic resonance imaging (MRI) scans,
● positron emission tomography (PET) CT scans,
● metaiodobenzylguanidine (MIBG) scans, and
● bone scans.
Ultrasound is often used initially to visualize abdominal masses and assess their characteristics. CT, MRI, and PET CT scans provide detailed images of the tumor’s:
● location,
● size, and
● involvement of nearby structures,
while MIBG and bone scans can detect metastases to bones or other distant sites.
In cases where imaging tests suggest the presence of neuroblastoma, a biopsy may be performed. This helps in obtaining a tissue sample for definitive diagnosis. Depending on the location and accessibility of the tumor, a biopsy may be conducted surgically. It can also be done by using image-guided techniques such as CT-guided needle biopsy. The biopsy sample is examined by a pathologist under a microscope. It helps in confirming the presence of neuroblastoma cells and to assess tumor characteristics, such as
● histology and
● genetic markers,
which can help guide neuroblastoma treatment decisions.
Furthermore, bone marrow aspiration and biopsy are commonly performed. It helps in evaluating the presence of neuroblastoma cells in the bone marrow. This is because neuroblastoma frequently metastasizes to the bone marrow. Bone marrow aspiration involves extracting a small sample of marrow fluid. On the other hand, a biopsy involves obtaining a small core of bone marrow tissue.
Analysis of bone marrow samples helps determine the extent of disease spread. It plays a critical role in staging neuroblastoma and determining prognosis. Collectively, these diagnostic procedures enable healthcare providers to accurately diagnose neuroblastoma. It helps them assess disease stage, and develop an individualized treatment plan tailored to each patient’s needs. Early and accurate neuroblastoma diagnosis is essential. This helps in initiating timely interventions and improving treatment outcomes for patients.
Neuroblastoma treatment in India follows a multidisciplinary approach, incorporating various modalities. The treatment plan is tailored to each patient’s specific circumstances, including:
● the stage of the disease,
● tumor characteristics, and
● overall health status.
Surgery plays a crucial role in the treatment of neuroblastoma. This is particularly in cases where the tumor is localized and can be safely removed. Skilled pediatric surgeons in India perform surgical procedures. They excise the primary tumor and, if feasible, remove any nearby lymph nodes or metastatic lesions. Complete surgical resection of the tumor may offer the best chance of cure. This is especially in early-stage neuroblastoma.
For patients with high-risk neuroblastoma, stem cell transplant may be recommended. This is also known as bone marrow transplant. Stem cell transplant involves:
● the infusion of healthy stem cells into the patient’s bloodstream
● following high-dose chemotherapy or radiation therapy.
This procedure helps replenish the bone marrow. It also helps restore blood cell production. This allows for higher treatment doses and potentially improved outcomes.
Chemotherapy is commonly used in the treatment of neuroblastoma. It helps:
● shrink tumors,
● control disease spread, and
● eradicate cancer cells throughout the body.
Pediatric oncologists in India administer chemotherapy drugs. It can be before surgery (neoadjuvant therapy) to reduce tumor size. In many cases, it can be after surgery (adjuvant therapy) to eliminate any remaining cancer cells. Chemotherapy regimens may vary based on the individual patient’s needs and may include a combination of drugs such as:
● cisplatin,
● etoposide,
● doxorubicin,
● cyclophosphamide, and
● vincristine.
Iodine 131-metaiodobenzylguanidine (MIBG) therapy is a targeted form of radiation therapy. It is used specifically for neuroblastoma that has spread to distant sites in the body, such as:
● the bones or
● bone marrow.
In this treatment approach, radioactive iodine labeled with MIBG is administered intravenously. It allows selective accumulation in neuroblastoma cells. It helps deliver radiation directly to the tumor.
Radiation therapy may be used in the management of neuroblastoma to target and destroy cancer cells. This is particularly in cases where the tumor cannot be completely removed surgically or has spread to certain areas of the body. Radiation oncologists in India utilize advanced techniques such as:
● intensity-modulated radiation therapy (IMRT) or
● proton therapy
to precisely deliver radiation to the tumor site. It also helps minimize damage to surrounding healthy tissues.
Immunotherapy has emerged as a promising treatment option for neuroblastoma. This is particularly for patients with high-risk disease. And even for those who have relapsed after standard treatments. Immunotherapy agents such as dinutuximab beta (anti-GD2 monoclonal antibody) stimulate the immune system. It helps to recognize and attack neuroblastoma cells. Pediatric oncologists in India may incorporate immunotherapy into treatment protocols. This can be done either alone or in combination with other therapies. It helps to enhance treatment efficacy and reduce the risk of disease recurrence.
Life after neuroblastoma treatment in India offers hope and a new beginning for patients and their families. With advancements in neuroblastoma treatment in India, including:
survivors can transition into a life free from the burden of cancer. Through
Follow-up care for neuroblastoma survivors is crucial. This helps in:
tailored to each patient’s individual needs. Pediatric oncologists and multidisciplinary healthcare teams work together and develop personalized follow-up plans. These plans are based on factors such as:
Follow-up visits typically include:
Additionally, survivors may receive screenings for late effects of treatment, such as:
to address any potential long-term complications. Psychosocial support services, including
are also available to help survivors and their families get through the emotional and practical challenges.
India stands out as one of the leading countries for neuroblastoma treatment, offering:
Neuroblastoma treatment in India combines cutting-edge therapies, including:
with personalized care tailored to each patient’s needs. India provides affordable neuroblastoma treatment options. This answers the common questions about neuroblastoma surgery cost in India. Patients and their families can benefit from:
As a result, India emerges as a top choice for neuroblastoma treatment.
There are various factors to be considered to choose the finest neuroblastoma treatment hospital in India. To ensure optimal care and outcomes for patients, one should consider these tips and conduct thorough research.
Here are some tips to guide your decision:
Specialization and Expertise: Choose hospitals with specialized pediatric oncology departments or cancer centers. They have dedicated teams of experts experienced in diagnosing and treating neuroblastoma. Consider factors such as:
Advanced Technology and Facilities: Assess the hospital’s infrastructure and technological capabilities, including:
State-of-the-art technology enhances the accuracy of diagnosis and treatment. It helps improve outcomes for neuroblastoma patients.
Comprehensive Services: Choose hospitals that offer full-range of neuroblastoma treatment options, including:
Quality and Accreditation: Examine the hospital’s quality standards and accreditations. Ensure adherence to international healthcare standards and patient safety protocols. Accreditation by organizations such as:
reflects commitment to excellence in healthcare delivery.
Cost and Affordability: Compare the different neuroblastoma surgery or treatment cost in India. Additionally, consider factors such as:
Look for hospitals that offer:
Research and Innovation: Choose hospitals that partake in clinical research and innovation. Access to:
may offer additional options for patients with challenging cases or treatment-resistant disease.
Location and Accessibility: Consider the hospital’s location. This means proximity to your home or accommodation. Additionally, check for accessibility in terms of transportation and travel logistics. Choose a hospital that is easily accessible and convenient. This will benefit you for regular appointments, follow-up visits, and ongoing care.
Patient Reviews and Testimonials: Seek feedback from other patients or their families. Those who have undergone treatment at the hospital can provide first-hand experiences. Patient reviews and testimonials also help. Insights into the hospital’s facilities and services can help you make an informed decision.
How to choose the best oncologist for your Neuroblastoma treatment in India?
Consider certain factors while choosing the best oncologist for neuroblastoma treatment in India. This is to ensure expertise, experience, and personalized care. Firstly, it’s crucial to seek out oncologists who specialize specifically in pediatric oncology. They should also have a proven track record in diagnosing and treating neuroblastoma. Look for oncologists affiliated with reputable hospitals or cancer centers. They should be known for their excellence in neuroblastoma treatment in India. These institutions often have multidisciplinary teams comprising:
When selecting an oncologist, consider their experience and expertise in managing neuroblastoma cases. They must also have familiarity with the:
Look for oncologists who have extensive experience in performing:
Additionally, consider their involvement in clinical research. Check for their participation in international collaborations aimed at advancing neuroblastoma treatment.
Another significant factor is Neuroblastoma surgery cost consideration. Evaluate the neuroblastoma treatment cost in India across different hospitals and oncology practices. This includes expenses related to:
While neuroblastoma surgery cost is important, prioritize value and quality of care over price alone. Some hospitals may offer:
to help manage neuroblastoma treatment costs in India. Therefore, inquire about these options during your consultation.
Patient reviews and testimonials can provide valuable insights into the oncologist’s reputation. Seek feedback from other neuroblastoma patients or their families. Those who have received treatment from the oncologist you are considering can help. Their firsthand experiences can assist you in gauging the oncologist’s dedication to patient care.
Finally, consider factors such as the oncologist’s:
Choose an oncologist who is conveniently located and accessible. Especially if you would require frequent visits or ongoing treatment. Ensure effective communication and a collaborative relationship between the parties involved. This will help in navigating the complexities of neuroblastoma treatment in India.
The neuroblastoma treatment cost in India can vary depending on several factors, including:
It’s essential to understand the components that contribute to the overall cost of treatment. It is better to consider various factors when estimating expenses.
Neuroblastoma treatment in India involves a multidisciplinary approach, incorporating various modalities such as:
The cost of each treatment modality can vary significantly. Surgery and chemotherapy are often being primary components of the treatment regimen.
Surgery for neuroblastoma may involve:
Neuroblastoma surgery cost in India depends on factors such as:
Chemotherapy is another critical aspect of neuroblastoma treatment. It is aimed at shrinking tumors, controlling disease spread, and eradicating cancer cells. The cost of chemotherapy varies based on:
Additionally, other treatment modalities such as:
based on the patient’s individual circumstances and disease characteristics. Each of these modalities incurs its own set of costs, including:
Apart from treatment-specific expenses, other factors such as:
While neuroblastoma treatment cost in India may be lower compared to many Western countries, it’s essential to consider:
Many hospitals in India offer:
Neuroblastoma is a relatively rare cancer, accounting for around 6% of all cancers in children. It is the most common solid tumor outside the brain in infants and young children. Approximately 800 new cases are diagnosed in the United States each year.
Neuroblastoma treatment outcomes have improved over the years. However, achieving a 100% cure rate remains a challenge. In India, comprehensive treatment options, including: 1. surgery, 2. chemotherapy, and 3. radiation therapy, combined with advanced techniques and supportive care. This offers high cure rates for many patients, but individual outcomes may vary.
Currently, there are no known preventive measures for neuroblastoma. The exact cause of neuroblastoma remains unclear, making prevention challenging. However, research into genetic and environmental factors may help identify potential risk factors. This is followed by preventive strategies in the future.
If you notice any symptoms suggestive of neuroblastoma, such as: 1. abdominal swelling, 2. bone pain, 3. unexplained weight loss, or 4. changes in bowel or bladder habits in your child, it’s essential to schedule an appointment with a healthcare provider promptly. Early detection and diagnosis are crucial for initiating timely treatment and improving outcomes.
Neuroblastoma most commonly occurs in infants and young children. The average age of diagnosis being around 18 months. However, it can also occur in older children and rarely in adults.
.Neuroblastoma has variable outcomes depending on factors such as: 1. the stage of the disease, 2. age at diagnosis, and 3. response to treatment. Overall, the mortality rate for neuroblastoma is higher compared to some other pediatric cancers. However, advancements in treatment have led to improved survival rates in recent years.
Neuroblastoma is typically diagnosed during early childhood. The majority of cases occurs before the age of 5 years. However, it can be diagnosed at any age, including infancy and adolescence.
Yes, neuroblastoma has a tendency to metastasize or spread to other parts of the body, most commonly to: the bones,bone marrow,lymph nodes,liver, and skin. Metastatic disease often affects treatment outcomes and prognosis.
While neuroblastoma is primarily a childhood cancer, it can rarely occur in adults. However, adult-onset neuroblastoma is extremely rare and comprises a small percentage of all cases.
Neuroblastoma occurs slightly more frequently in boys than girls, with a male-to-female ratio of approximately 1.2 to 1. However, the difference in incidence rates between genders is relatively small
Yes, the age at diagnosis can significantly impact the outcome of neuroblastoma patients. Younger children tend to have better survival rates compared to older children and adults. This is particularly those diagnosed before 18 months of age.
24/7 Assistance with the best medical care at your service
Quality treatment with professional & unmatched personal care
Our experts make your Communication easier and more transparent