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Endocrine Pancreas

Rare Tumors. Right Diagnosis. Precise Surgery.

Endocrine tumors of the pancreas are uncommon but require expert evaluation and specialized treatment. These tumors arise from hormone-producing cells in the pancreas and can either be functional (hormone-secreting) or non-functional. At our center, we provide comprehensive care, from early diagnosis to advanced surgical treatment of these rare but serious conditions.

Types of Pancreatic Neuroendocrine Tumors (PNETs)

Insulinoma

A benign tumor that may or may not secrete excess hormones. Often discovered incidentally during imaging for other reasons.

Gastrinoma (Zollinger-Ellison Syndrome)

A benign tumor of one parathyroid gland that causes excess PTH production. Surgical removal cures the condition.

Glucagonoma

Produces glucagon, leading to high blood sugar, skin rashes, weight loss, and anemia.

Somatostatinoma

A rare cancerous growth of the parathyroid gland that can cause severe hypercalcemia and complications.

VIPoma

Caused by excess cortisol production, leading to weight gain, facial puffiness, muscle weakness, and easy bruising.

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