Pituitary spindle cell oncocytoma: Two cases report and literature review.

INTRODUCTION

Pituitary spindle cell oncocytoma (PSCO) is a seldom-encountered type of pituitary neoplasm with distinctive histological features. It was first described as a distinct entity by Roncaroli et al. in 2002. We present two cases of PSCO and discuss its clinical, radiological, and histopathological features, along with a review of the existing literature.

PRESENTATION OF CASE: Two cases underwent trans-nasal transsphenoidal surgery for tumor resection and had different treatment following would be discussed in this article. Both had unique pathology pattern as Pituitary spindle cell oncocytoma.

DISCUSSION: Tumors positive for TTF-1 in the sellar region, such as pituicytoma, granular cell tumor, and spindle cell oncocytoma, originate from the posterior pituitary gland and are rare. The expression of thyroid transcription factor-1 (TTF-1) in these tumors aids in distinguishing them from other pituitary neoplasms.

CONCLUSION

Pituitary spindle cell oncocytoma is a rare entity among pituitary tumors. This case report highlights the clinical, radiological, histopathological, and immunohistochemical features of PSCO. Surgeons and pathologists should consider this rare diagnosis in patients with sellar and suprasellar masses, as early recognition and complete surgical resection can lead to favorable outcomes.