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Assessment of Ovarian Cancer Spheroid Attachment and Invasion of Mesothelial Cells in Real Time
Published on: May 20, 2014
Insulin producing primary ovarian carcinoid tumor
Nils-Halvdan Morken1, Bernard Majak, Jarl A Kahn
1Department of Obstetrics and Gynecology, Telemark Hospital, Skien, Norway. nhmorken@online.no
Acta Obstetricia Et Gynecologica Scandinavica
|May 9, 2007
Summary
This report details the first known case of an insulin-producing primary ovarian carcinoid tumor. This rare ovarian cancer was successfully treated with surgery after presenting with amnesia and hypoglycemia.
Area of Science:
- Endocrinology
- Gynecologic Oncology
- Oncology
Background:
- Carcinoid tumors, typically slow-growing, most commonly originate in the gastrointestinal tract.
- Primary ovarian carcinoid tumors are exceptionally rare, accounting for less than 0.1% of all ovarian carcinomas.
- These tumors can also arise in genital tissues, including the ovaries.
Observation:
- The case involved a patient presenting with amnesia and hypoglycemia.
- These symptoms were indicative of an underlying endocrine disorder.
- The diagnostic process identified an insulin-producing tumor.
Findings:
- The first documented case of an insulin-producing primary carcinoid tumor of the ovary is presented.
- The tumor was successfully treated with surgical intervention.
- This finding expands the known spectrum of ovarian carcinoid tumors.
Implications:
- Highlights the importance of considering rare endocrine tumors in the differential diagnosis of unexplained neurological and metabolic symptoms.
- Demonstrates that surgical resection can be an effective treatment for this rare ovarian malignancy.
- Contributes to a better understanding of the pathophysiology and clinical presentation of ovarian carcinoid tumors.

