J Korean Neurosurg Soc.  2006 Dec;40(6):459-462.

Atypical Granular Cell Tumor of the Sellar Region

Affiliations
  • 1Departments of Neurosurgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea. kwanmd.park@samsung.com
  • 2Departments of Pathology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

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.

Keyword

Atypical granular cell tumor; Suprasellar; Neurohypophysis; Central nervous system

MeSH Terms

Central Nervous System
Diagnosis
Female
Granular Cell Tumor*
Humans
Middle Aged
Pathology
Pituitary Gland
Pituitary Gland, Posterior
Pituitary Neoplasms
S100 Proteins
S100 Proteins
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