Granular Cell Pituitary Tumor in a Patient with Multiple Endocrine Neoplasia-1

Abstract

Multiple endocrine neoplasia type 1 (MEN-1) is an autosomal dominant disorder characterized by parathyroid, pancreatic islet, and pituitary tumors. Approximately 40% of MEN-1 patients harbor a pituitary adenoma. Separately, granular cell tumors (GCTs) of the sellar/parasellar region are an exceedingly rare clinical entity with less than 100 reported cases in the literature. These slow-growing, often asymptomatic lesions are difficult to diagnose and may mimic pituitary adenoma, Rathke cleft cyst, or other sellar/supra-sellar pathology. There is no known association with MEN-1 or any other familial syndrome. A 36-year-old neurologically normal woman with known MEN-1 underwent a screening magnetic resonance imaging (MRI) scan which revealed a 10 mm x 6 mm x 7 mm sellar/suprasellar lesion. She underwent endoscopic endonasal transsphenoidal resection. Subsequent neuropathological analysis was consistent with GCT of the pituitary gland. Here we describe the first report to our knowledge of a GCT of the pituitary gland occurring in a patient with MEN-1.

Multiple endocrine neoplasia type 1 with refractory hypoglycemia and lung and liver metastases: a case report

“…The liquefaction area is not enhanced, and calcification is rarely seen as a scattered dot or block. 5 (2) MRI is generally used in coronal and sagittal thin layers (<3 mm). Pituitary tumor shows low signal on T1WI, but a mixed high/low signal in tumor with hemorrhage.…”