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Updated: Jun 11, 2026

Robotic Enucleation of an Intra-Pancreatic Insulinoma in the Pancreatic Head
Published on: January 3, 2020
Case reports of insulinoma and nesidioblastosis in Ethiopia
Moges Kibebew1, Seifu Bacha, Yeweyenharge Feleke
1Department of Internal Medicine, Faculty of Medicine, Addis Ababa University.
Abstract:
We present history, physical examination, diagnosis and histological findings of one case of insulinoma and another case of nesidioblastosis. Insulinoma is a rare endocrine tumor, which is usually benign, characterized by hypoglycemic symptoms. The first case presented with seizure, which made diagnosis difficult. The second case presented with typical hypoglycemic symptoms. Both cases underwent partial pancrectomy and splenectomy after workup. The histology of the first case was consistent with insulinoma, while the second case was that of nesidioblastosis.
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