Abstract

IntroductionSpindle cell oncocytoma of the adenohypophysis is a rare tumour recently reported by Roncaroli et al. in 2002. This tumour is considered a grade I tumour by the World Health Organization.Case presentationWe describe what is, to the best of our knowledge, the 14th case of its kind in the literature. A 45-year-old African woman presented clinical and radiological findings related to a nonfunctioning pituitary adenoma. The diagnosis was made on the basis of histological and immunohistochemical findings.ConclusionThe purpose of this work is to report a rare pituitary tumour and to describe its histological and immunohistochemical features, which were characterized by the expression of thyroid transcription factor 1 antigen by tumour cells. This fact could support the theory of a possible common origin of these tumours in pituicytomas. In fact, thyroid transcription factor 1 is considered to be a specific marker of pituicytes.

Highlights

  • Spindle cell oncocytoma of the adenohypophysis is a rare tumour recently reported by Roncaroli et al in 2002

  • The purpose of this work is to report a rare pituitary tumour and to describe its histological and immunohistochemical features, which were characterized by the expression of thyroid transcription factor 1 antigen by tumour cells

  • This fact could support the theory of a possible common origin of these tumours in pituicytomas

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Summary

Introduction

Spindle cell oncocytoma of the adenohypophysis is a rare tumour recently reported by Roncaroli et al in 2002. This tumour is considered a grade I tumour by the World Health Organization. Spindle cell oncocytoma (SCO) of the pituitary gland is a recently described entity which was recognized by the 2007 WHO Classification of Brain Tumours and considered a WHO grade I tumour [1]. It was initially described by Roncaroli et al in 2002 [2], and only 14 cases have been reported in the literature.

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