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Somatostatinoma is
a rare neuroendocrine tumor that usually develops in the pancreas or duodenum
and may produce excess somatostatin, a hormone that suppresses several
digestive and metabolic functions. It often causes vague symptoms such as abdominal
pain, weight loss, diarrhea, jaundice, and in some cases the classic “somatostatinoma
syndrome” with diabetes, gallstones, steatorrhea, and low stomach
acid. Because the symptoms are non-specific, diagnosis is often delayed
until the tumor has grown or spread.
Treatment usually depends on
the size and location of the tumor, but surgery is the main option when
the disease is localized. Advanced cases may need additional therapies such as chemotherapy,
radiation, or targeted medicines.