[A Patient with Multiple Endocrine Neoplasia Type1(MEN1)Presenting with Hypoglycemic Attacks]
Kazuhiko Bando1, Daizo Ebisutani
1Department of Neurosurgery, Anankyoei Hospital.
No Shinkei Geka. Neurological Surgery
|May 1, 2015
Summary
This case study details a Multiple Endocrine Neoplasia type 1 (MEN1) patient with recurrent hypoglycemia. Diagnosis involved identifying insulinomas after ruling out other causes, leading to successful tumor resection and symptom resolution.
Area of Science:
- Endocrinology
- Oncology
- Neurosurgery
Background:
- Multiple Endocrine Neoplasia type 1 (MEN1) is a rare genetic disorder.
- MEN1 can manifest with tumors in the parathyroid, pituitary, and pancreas.
- Hypoglycemia is a critical symptom requiring prompt diagnosis and management.
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