Atypical Granular Cell Tumor of the Sellar Region.
- Author:
Deok Joo RHEE
1
;
Yoon La CHOI
;
Yeon Lim SUH
;
Kwan PARK
Author Information
1. Departments of Neurosurgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea. kwanmd.park@samsung.com
- Publication Type:Case Report
- Keywords:
Atypical granular cell tumor;
Suprasellar;
Neurohypophysis;
Central nervous system
- MeSH:
Central Nervous System;
Diagnosis;
Female;
Granular Cell Tumor*;
Humans;
Middle Aged;
Pathology;
Pituitary Gland;
Pituitary Gland, Posterior;
Pituitary Neoplasms;
S100 Proteins
- From:Journal of Korean Neurosurgical Society
2006;40(6):459-462
- CountryRepublic of Korea
- Language:English
-
Abstract:
We report a very rare case of atypical granular cell tumor arising in the neurohypophysis of a 56-year-old woman. The tumor was seen on radiology to be lobulated, soft and diffusely enhanced, the same as pituitary macroadenoma, but it was anatomically localized within the posterior part of the hypophysis. We partially removed the tumor via the transsphenoidal approach. The pathology showed nuclear pleomorphism, spindling features, and lymphoplasmacytic infiltration. Ki-67 and S-100 protein were focally positive in tumor cells. Histological diagnosis confirmed an atypical granular cell tumor in the sellar region, which is a rare tumor that often has the clinical appearance of a pituitary adenoma. Ophthalmologic symptoms are the most common, followed by endocrinologic manifestations. Here we describe its symptoms and radiological and pathological features.
