Insulinoma

Authors

  • Ria Yuniarti Departemen Patologi Anatomi, Fakultas Kedokteran Universitas Sriwijaya, Palembang, Indonesia Author
  • Suly Auline Departemen Patologi Anatomi, Fakultas Kedokteran Universitas Sriwijaya, Palembang, Indonesia Author

Keywords:

Insulinoma, Neuroendokrin, Insulin, Tumor Pankreas, Hipoglikemia, Hiperinsulinemia

Abstract

Insulinoma is a functional neuroendocrine neoplasm consisting of insulin-producing
cells, which produce insulin uncontrollably, causing a hypoglycemic syndrome. The
Hypoglycemic syndrome is a result of hyperinsulinemia which causes adrenergic
symptoms and neuroglycopenia. The clinical diagnosis is based on the Whipple triad,
insulin, and C peptide levels in a 72-hour fasting state. Generally, insulinoma is a
benign neoplasm with a proliferation index of Ki-67 <2%. On histological features, the
growth pattern of the insulinoma is usually trabecular or solid. Some insulinomas show
a tubuloacinar growth pattern with psammoma bodies. We reported one case of
insulinoma in a 65-year-old woman, who had experienced fainting, cold sweats for 3
years, especially when the patient ate late or at midnight while sleeping. A CT scan
showed a tumor mass in the pancreas possibly an insulinoma and a pancreatectomy
was performed. The results of the histopathological examination are bu following peer
under Insulinoma.

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Published

31-12-2020

How to Cite

Ria Yuniarti, & Suly Auline. (2020). Insulinoma. Jurnal RSMH Palembang, 1(2), 78-85. https://jurnal.rsmh.co.id/index.php/jrp/article/view/10