The rare disease came into the spotlight after actor Irrfan Khan revealed that he had been diagnosed with it.
Early detection, appropriate therapy key to treating neuroendocrine tumour: Expert
New Delhi - 16 Mar 2018 20:00 IST
Neuroendocrine tumour — a rare disease that came into the spotlight with actor Irrfan Khan revealing on Friday that he has been diagnosed with it — is treatable if detected early, a city-based neurologist said.
The disease, which according to doctors is a "quite rare disease and more common in males in the age group 30-50", occurs in less than one per million cases. It is rare in both the general population as well as in patients with malignancies of tumour.
According to Vinit Suri, senior consultant, neurology, Indraprastha Apollo Hospitals, "early detection can lead to cure by excising the tumour or giving appropriate therapy".
However, in Khan's case, he has not yet revealed which stage of the condition he is suffering or whether it is malignant or not.
Neuroendocrine tumour is a condition in which the neuroendocrine cells — that perform specific functions such as regulating air and blood flow through the lungs and controlling how quickly food moves through the gastrointestinal tract — develop into tumours.
While a neuroendocrine tumour can grow in lungs or a small gland behind the breastbone called the thymus, or more rarely, in the pancreas, kidneys, ovaries, or testicles, "the most common is lung, pancreas and intestines", Suri informed.
Depending on the location of the tumour, the tumours may develop local symptoms.
For example, if the tumour is in the lungs, patients may experience cough, bleeding in sputum, chest pain; if it grows in the intestines, patients may develop diarrheoa, bleeding and have black stools.
"Because an endocrine tumour develops from cells that produce hormones, the tumour can also produce hormones. This can cause serious illness including palpitation, high or low BP, which may be precursors to various cardiovascular diseases," Suri noted.
The disease can also be genetically predisposed. Thus, for people with a family history, early screening is a must, the doctor suggested.
Treatment depends on the type, that is whether it is benign or malignant and the location of the tumour.
"Waiting for the disease to become symptomatic can make it incurable," the neurologist said.