Pancreatic Neuroendocrine Tumors Treatment in United Arab Emirates
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What are Pancreatic Neuroendocrine Tumors?
Pancreatic neuroendocrine tumours (PNETs) are a rare group of tumours arising from the neuroendocrine cells of the pancreas that produce hormones, including insulin, glucagon, somatostatin, etc. These tumours may be benign or malignant, and they usually grow more slowly than other pancreatic tumours, most notably pancreatic adenocarcinoma.
What is the Importance of Timely Treatment?
- Improved Prognosis: The chances of curing or controlling the disease are substantially better with treatment when detected early, including surgical tumour removal. Early interventions lead to long-term survival in localised tumours.
- Preventing Complications: PNETs can lead to complications like hormonal imbalances (e.g., hypoglycemia in insulinomas), pain, or jaundice. Prompt intervention treats the tumours to relieve symptoms and prevent serious complications.
- Reduced Risk of Metastasis: Early diagnosis increases the possibility of metastasis to some distant organs. However, timely therapy can prevent the tumour from progressing and spreading to various organs like the liver.
- Better Life: Early treatments will help control symptoms, pain, and discomfort caused by more extensive or invasive tumours.
What are the Common Symptoms of Pancreatic Neuroendocrine Tumors?
- Hypoglycemia (Low Blood Sugar)
- Hyperglycemia (High Blood Sugar) or Diabetes
- Abdominal Pain
- Unexplained Weight Loss
- Jaundice
- Nausea and Vomiting
- Fatigue
- Palpitations or Rapid Heartbeat
Causes and Risk Factors of Pancreatic Neuroendocrine Tumors
Causes
- Genetic Mutations
- Endocrine Disruptions
- Sporadic Development
Risk Factors
- Genetic Syndromes
- Age
- Family History
- Hormonal Imbalances
- Environmental Factors
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Latest Research and Technologies in the Treatment of Pancreatic Neuroendocrine Tumors in the United Arab Emirates
Novel approaches to treating pancreatic neuroendocrine tumors (PNET) are now directed towards precision medicine and targeted therapeutic avenues. Peptide receptor radionuclide therapy (PRRT) has paved the way for one of the most innovative breakthroughs, providing targeted radiation to tumor cells. Next-gen sequencing enables personalised treatment by revealing the presence of specific mutations in patients. Minimally invasive robotic and laparoscopic surgery programs lead to quicker recovery with better outcomes. Immunotherapy and targeted agents such as everolimus and sunitinib are used to slow the growth of tumors.
Pancreatic Neuroendocrine Tumors Prevention Tip:
- Genetic Counseling and Screening: Normal screening and genetic counselling are preventive measures in the timely diagnosis of PNETs for people with a familial history of genetic syndromes, such as MEN1 or von Hippel-Lindau disease.
- Healthy lifestyle choices: Consume a healthy, balanced diet full of fresh fruits, vegetables and whole grains while reducing the levels of processed foods and red meat.
- Avoid Smoking: Smoking is a known carcinogen in most cancers, including the pancreatic types and possibly the PNETs.
- Confirming early detection for high-risk individuals: Individuals with a familial history of endocrine tumours are offered, subject to regular imaging and blood tests to check for possible tumours.
- Management of chronic pancreatitis: Chronic pancreatitis can be managed effectively by medical treatment as it prevents possible PNET development.
Treatment options for Pancreatic Neuroendocrine Tumors
The medical treatment for Pancreatic Neuroendocrine Tumors requires evaluating the patient's severity and medical condition. The following are the treatment options:
Surgical Resection: Surgical tumour removal is the most effective treatment option for localised PNETs. Thus, surgery provides the best chance of cure or long-term control in the case of a tumour localised to the pancreas.
Targeted Therapy : Targeted therapies inhibit tumour growth in advanced-stage or metastatic PNET cases. These therapies help slow down disease progression and enhance survival.
Cost Start From USD 5500 - USD 54000Explore Options
Chemotherapy: Chemotherapy with medications is used in aggressive or metastatic PNETs. Chemotherapy is most often used when surgery or targeted therapy proves ineffectual in curbing the disease.
Cost Start From USD 800 - USD 6000Explore Options
Whipple Procedure (Pancreaticoduodenectomy) : This procedure is performed for localised and resectable tumours. It is intended for functional or non-functional PNETs localised within the pancreas.
Cost Start From USD 18000 - USD 22000Explore Options
Stereotactic Radiotherapy (SRT) is the treatment modality for localised, inoperable, or metastatic PNETs when surgery is not performed. It is also for patients who cannot undergo surgery or whose disease has already spread to other sites.
Cost Start From USD 14500 - USD 0Explore Options
CyberKnife : The CyberKnife system is typically beneficial in managing small to medium-sized tumours that have proven inoperable, are subject to difficult surgical excision, or have metastasised into surrounding organs or tissue planes.
Cost Start From USD 5000 - USD 10000Explore Options
Proton Therapy : Proton therapy is for such out-of-sight or inoperable PNETs. Given its significance in tumours near critical structures such as blood vessels or the spine, it is also applicable in treatment for metastatic PNETs when the cancer has spread elsewhere.
{proton-therapy}These are the standard diagnostic methods for diagnosing Pancreatic Neuroendocrine Tumors:
Imaging Studies
- CT Scan: This is one of the most common imaging techniques used for PNET detection, i.e. determining tumour size, location, and evidence of metastasis, if any, especially to the liver or lymph nodes.
- MRI generates high-definition images of the pancreas, particularly for delineating soft tissue and assessing the extent of the tumour.
- Endoscopic Ultrasound: Provides even better imaging of the pancreas and surrounding structures and allows guidance for fine-needle aspiration (FNA) to acquire biopsy samples.
- Positron Emission Tomography: It plays a vital role in tracking a radioactive glucose analogue to locate areas of high metabolic activity associated with malignant tumours.
Biopsy
- Fine Needle Aspiration: Fine needle aspiration techniques, usually done following some imaging modality that indicates tumour presence, are said to be concurrent with an essential ultrasound study, during which tissue samples are taken for histopathological examination, thus confirming the diagnosis of PNETs.
- Core Needle Biopsy: If a more definitive diagnosis is needed, a small core needle biopsy can be performed to obtain a tissue sample.
Blood Tests
- Tumour Markers: Serum tumour markers such as chromogranin A (CgA) and pancreatic polypeptide (PP) can be other means of blood work to diagnose PNETs; elevated levels strongly suggest the presence of neuroendocrine tumours in the patient.
Somatostatin Receptor Scintigraphy (SRS)
- Octreotide Scan: This technique uses radioactive tracers bound to somatostatin to detect somatostatin receptors on neuroendocrine tumour cells. It is generally applicable in detecting localised, nonmetastatic PNETs amenable to surgical intervention.
MediRehab (a chain of Rehab centres, part of MediGence) provides comprehensive rehabilitation services to support patients through Teleconsulations and online therapy sessions.
- Rehabilitation following Surgery: Postoperative rehabilitation aims to help patients return to their daily lives after surgical tumour excision by regaining strength and improving mobility.
- Lifestyle modification: Nutritional counselling is a must for patients, especially after pancreatic surgery, as they will experience some digestive problems due to the diminished function of the pancreas.
- Pain Management: For those who experience pain after treatment, especially surgery or chemotherapeutic agents, it will be helpful to return to pain management therapy after these therapies.
- Hormone and Endocrine Therapy: Patients with functional PNETs (producing excess hormones) may require hormonal therapy to manage their symptoms of hypoglycemia, gastric issues, etc.
- Psychosocial Support: A diagnosis of cancer creates a stir in the mind and soul of a patient. Counselling, support groups or any form of mental help assists patients and families in bearing the emotional aspects of this disease, PNET.
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Hospitals for Pancreatic Neuroendocrine Tumors in United Arab Emirates
Zulekha Hospital Sharjah
Sharjah, United Arab Emirates
Zulekha Hospital Sharjah located in Sharjah, United Arab Emirates is accredited by ISO, JCI. Also listed below are some of the most prominent infrastructural details:
- Zulekha Hospital Sharjah is present over a 290,000 square feet area.
- The hospital stands today with a bed capacity of 185.
- The hospital also has a Cardiac Catheterization Laboratory and radiology as well as laboratory services.
- There is an ICU and Neonatal ICUs.
- There are facilities for Dialysis and advanced technological applications such as Minimal Invasive surgeries.
- In Zulekha Hospital Sharjah Bariatric procedures, Joint Replacement, Specialised Cancer Care, Cardio Thoracic and Vascular Procedure, Plastic and Reconstructive Procedure are performed.
- It also specialises in Pediatric Cardiology, Pulmonology and Chest Diseases, etc.
- Teleconsultation services as well as an international patient care center with related assistance for medical travelers are functioning in Zulekha Sharjah.
Burjeel Medical City
Abu Dhabi, United Arab Emirates
The Hospital owns an International Patient Services Team that is responsible to assist international patients with world-class healthcare, transportation arrangement, accommodation facilities, language interpreters, and much more.
Burjeel Medical City (about 1.2 million square facilities)provides 7-star hospitality to its patients. It has the largest facility space bed among all the private hospitals. The Hospital consists of-
- Large waiting areas and consultation rooms
- Spacious lobbies on each floor
- 338 Luxurious Patient Rooms
- 70 Ambulatory Rooms
- Intensive Care Units
- The Hospital comprises various centers, under Burjeel Cancer Institute-
- Breast Center
- Uro-oncology Center
- Surface Malignancy Center (HIPC)
- Head & Oncology Center
- Medical Oncology & Hematology Center and others
Zulekha Hospital Dubai
Dubai, United Arab Emirates
Zulekha Hospital Dubai located in Dubai, United Arab Emirates is accredited by ISO, JCI. Also listed below are some of the most prominent infrastructural details:
- The bed capacity of Zulekha Hospital Dubai is 140.
- Diagnostic centers, pharmacies, inpatient and outpatient care are provided at Zulekha Hospital Dubai.
- This hospital provides the best of healthcare packages
- Its surgical base is really strong with the hospital having successfully initiated and completed minimally invasive surgeries, joint replacement surgeries, bariatric surgeries, cardiac, and neonatal surgeries.
- Radiology, laboratory, operating theatres, dialysis section and Cardiac Catheterization Laboratory are all present in Zulekha Hospital Dubai, UAE.
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Why Choose the United Arab Emirates for Pancreatic Neuroendocrine Tumor Treatment?
The following are the growing reasons for the United Arab Emirates being frequented for Pancreatic Neuroendocrine Tumor treatment:
- Advanced Oncology Centres: The United Arab Emirates boasts children’s hospitals with modern procedures for ACC.
- Expert Multidisciplinary Teams: Pediatric oncologists, surgeons, and radiologists cooperate to provide customised treatment.
- Minimally Invasive Surgery Options: Robotic and laparoscopic surgeries guarantee the fastest recovery with minimum scarring.
- Affordable World-Class Treatment: Wilms tumour care in the United Arab Emirates is high-standard yet more affordable than in other countries.
- Internationally accredited hospitals: JCI-accredited facilities treat cancer according to international protocols for safety and efficacy.
Frequently Asked Questions
Yes, surgeries in robotic and laparoscopic procedures are practised primarily for faster recovery.
The duration of treatment varies according to tumor type and stage but usually lasts several weeks to several months.
The prognosis of PNETs is based on the tumour's size, location, functional status, and the presence of metastases. Early detection and surgery are the best options for offering a good prognosis, whereas therapies must be combined with advanced or metastatic cases to manage PNETs.
Most PNETs are sporadic, although they can be combined with some genetic conditions, such as MEN1 syndrome and von Hippel-Lindau disease. Individuals with family histories of these conditions might require genetic counselling and regular screening.
Currently, there is no known preventive measure against PNETs. A healthy lifestyle that avoids smoking and genetic screening for higher-risk individuals can contribute to early detection and improved management of the disease.
Even after treatment, the PNETs can recur depending on whether the tumour was removed entirely or metastasised. Regular follow-up scans and monitoring are very crucial to detect recurrences at an early stage.
The treatment method used will determine the long-term effects. Surgical recovery can cause digestive problems, chemotherapy has intermediate side effects such as nausea and lethargy, and targeted therapies can cause skin rashes or fatigue. Regular follow-up care must ensure monitoring for recurrence or complications.
A nutritious diet, physical exercise, and abstinence from alcoholic beverages and smoking may enhance a patient's health. Hormone-secreting tumours may also require an individual to follow directed medical advice in managing portions of low blood sugar or digestive issues.