Medical Tourism India Reports Huge Increase In Patients For The Treatment Of Familial Adenomatous Po
Medical tourism in India reports huge increase in patients for the treatment of
Familial Adenomatous polyposis as international patients are getting best results that too at minimal cost. Treatment of Familial Adenomatous polyposis in India is provided by a multi-disciplinary medical team with high level and up-to-the-minute training and experience in their particular field of medicine and surgical care. The entire focus of the department, from the state-of-the-art equipment and facilities to leading drug development and treatment options, is centered on the needs of the patients. Indian hospitals offer a full range of post surgery professional holistic services, from nutrition and dietary advice, to complementary therapies and specialist counseling.What is Familial Adenomatous polyposis?
Familial Adenomatous polyposis is considered to be rare. In people with Familial Adenomatous polyposis, masses of noncancerous tissue tend to form in many different organs. These include:
Multiple adenomatous colon polyps (adenomatous polyps are areas where normal tissue that lines the inside of the colon that makes mucous build up into a mass on the inside of the intestinal tract)
Benign (noncancerous) tumors, including:
sebaceous cysts (closed sac filled with liquid found under the skin)
epidermoid cysts (lumps in or under the skin often filled with liquid)
fibromas (fibrous tumors)
desmoid tumors (fibrous tumors that can develop anywhere in the body)
osteomas (bony growths, usually found on the jaw)
People with Familial Adenomatous polyposis also have a higher risk of developing colorectal cancer and other FAP-related cancers. Other features of Gardner syndrome that are similar to classic FAP include extra or unerupted teeth and congenital (present at birth) hypertrophy of the retinal pigment epithelium (CHRPE), an eye condition that does not affect vision but which a doctor can find by doing an examination with a special instrument called an ophthalmoscope.
What causes Familial Adenomatous polyposis?
Familial Adenomatous polyposis is a genetic condition. This means that the risk of Familial Adenomatous polyposis can be passed from generation to generation in a family. The APC gene is linked to Familial Adenomatous polyposis; APC stands for adenomatous polyposis coli. A mutation (alteration) in the APC gene gives a person an increased lifetime risk of developing polyps, benign tumors, and cancer.
There are no specific symptoms.
If the polyps become very large, they may cause intestinal bleeding, Intussusception, orIntestinal Blockage. Otherwise, they may not cause any symptoms.
People with this disease also have a higher risk of developing dermoid tumors, abnormalities of the retina, skin tumors, and bone tumors.
The intestinal polyps usually appear by the early to mid teenage years. By age 35, almost all with this disease will have polyps.
Polyps in the colon will become cancerous in almost everyone with this disease by age 50.
Polyps are found in the stomach in over half of those affected with this disease. However, stomach polyps usually do not become cancerous.
Polyps are also found in the small intestine in over 90% of those with this disease, and tend to become cancerous in up to 10 to 15%.
How is Familial Adenomatous polyposis diagnosed?
A person with multiple adenomatous colon polyps and/or colorectal cancer along with some of the benign tumors listed above is suspected of having Gardner syndrome. People suspected to have Gardner syndrome can have a blood test to look for a mutation in the APC gene. If an APC gene mutation is found, other family members will be diagnosed with Gardner syndrome if they are tested and have the same gene mutation.
Treatment of Familial Adenomatous polyposis
There is no specific treatment for Familial Adenomatous polyposis.
People with this disease have a very high risk of developing cancer. In fact, almost all with this disease will develop cancer by the time they turn 50.
Therefore, those with this disease need to be checked and screened very carefully and very often for any abnormalities.
Also, all persons with this condition will need to have the entire colon removed. This is a preventive measure done to prevent cancer. Depending on the type of surgery, sigmoidoscopies will be needed afterward to make sure no cancer develops in remaining parts of the intestine. This will be determined by one's primary care doctor and the surgeon who performed the surgery.
Periodic upper endoscopy is used to make sure that cancer does not develop in the stomach or intestine, and will need to be continued even after the colon is removed.
Why India?
Treatment of Familial Adenomatous polyposis in India is done at the most sought after medical treatment centers, with the application of modern surgical technology. Medical tourism in India has a great deal of experience in meeting the cultural needs of international patients and offers a service which provides support from the moment a medical report is received right through to assistance with arranging transport home, ensuring international patients feel at ease about coming to India for treatment and feel at home during their stay. Medical tourism in India is merging with medical expertise and tourism providing high quality healthcare for Nigerian patients. For more information on Treatment of Familial Adenomatous polyposis in India, visit us at www.forerunnershealthcare.com or mail your queries at enquiry@forerunnershealthcare.com or call us at: +91-9371136499, +91- 9860755000 (International) / + 1-415-599-2537 (USA) / +44-20-8133-2571 (UK)
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