Granular cell tumor of the pituitary fossa

John S. Rhee, Phillip A. Wackym, Karin Hague, David Wolfe, Wesley A. King

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

Although granular cell tumors are relatively common in the head and neck, symptomatic granular cell tumors of the neurohypophysis are extremely rare. Ophthalmologic symptoms are most common, followed by endocrinologic manifestations. We report a case of a granular cell tumor of the pituitary fossa that was surgically treated. The clinical manifestations, radiographic appearance, and surgical management of granular cell tumors of the pituitary fossa are reviewed, as well as the unique histopathology and electron microscopy of this uncommon neoplasm.

Original languageEnglish
Pages (from-to)754-758
Number of pages5
JournalAnnals of Otology, Rhinology and Laryngology
Volume111
Issue number8
DOIs
StatePublished - 2002

Keywords

  • Granular cell tumor
  • Neurohypophysis
  • Pituitary neoplasm

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