Yip Chi-Man, Lee Huai-Pao, Hsieh Pin-Pen
Division of Neurosurgery, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan, R.O.C.
Department of Pathology and Laboratory Medicine, Kaohsiung Veterans General Hospital, Taiwan, R.O.C.
J Surg Case Rep. 2019 Jun 14;2019(6):rjz179. doi: 10.1093/jscr/rjz179. eCollection 2019 Jun.
Spindle cell oncocytoma is a rare nonfunctioning neoplasm of the adenohypophysis, and was first described in 2002 by Roncaroli In 2007, spindle cell oncocytoma has been categorized as a separate entity by the World Health Organization (WHO) and is classified as a Grade 1 tumor of the central nervous system. Spindle cell oncocytoma of pituitary gland usually occurs in adults and accounts for 0.1-0.4% of all sellar region tumors. Clinically and radiologically, they are indistinguishable from nonfunctioning pituitary adenomas. From 2002 to 2018, approximately 46 cases of spindle cell oncocytoma of pituitary gland had been reported in the English literature and we would like to report a case of 28-year-old woman presented with pituitary apoplexy proved to be a case of spindle cell oncocytoma of pituitary gland which probably will be the 47th reported case.
梭形细胞嗜酸细胞瘤是一种罕见的腺垂体无功能性肿瘤,于2002年由龙卡罗利首次描述。2007年,世界卫生组织(WHO)将梭形细胞嗜酸细胞瘤归类为一个独立的实体,并将其列为中枢神经系统1级肿瘤。垂体梭形细胞嗜酸细胞瘤通常发生于成年人,占所有鞍区肿瘤的0.1 - 0.4%。在临床和影像学上,它们与无功能性垂体腺瘤无法区分。从2002年到2018年,英文文献中报道了约46例垂体梭形细胞嗜酸细胞瘤病例,我们在此报告一例28岁女性垂体卒中患者,经证实为垂体梭形细胞嗜酸细胞瘤,这可能是第47例报道病例。