Boulis N M, Sathi S, Schwartz R, De Girolami U, Black P M
Department of Neurosurgery, Radiology, and Pathology, Brigham and Women's Hospital, Boston, Massachusetts.
Surg Neurol. 1994 Jun;41(6):494-7. doi: 10.1016/0090-3019(94)90015-9.
A unique case of a suprasellar hamartoma in a 29-year-old woman is presented. The lesion was discovered in the context of a work-up for amenorrhea that had lasted 1 year and was resistant to clomiphene and medroxyprogesterone acetate treatment. Magnetic resonance imaging (MRI) revealed a 1.2-cm anterior suprasellar lesion with no apparent connection to the hypothalamus or hypophysis. She underwent surgical resection of the mass. Pathologic examination revealed randomly arranged mature neurons, glial tissue, and myelinated fibers. There was no evidence of gonadotropin-releasing hormone producing neurons on immunohistochemical studies. Postoperative MRI showed complete resection of the lesion, and 1 year later mensus resumed off medication.
本文介绍了一名29岁女性蝶鞍上错构瘤的独特病例。该病变是在对持续1年且对克罗米芬和醋酸甲羟孕酮治疗耐药的闭经进行检查时发现的。磁共振成像(MRI)显示蝶鞍前上方有一个1.2厘米的病变,与下丘脑或垂体无明显联系。她接受了肿块的手术切除。病理检查显示有随机排列的成熟神经元、神经胶质组织和有髓纤维。免疫组织化学研究未发现促性腺激素释放激素产生神经元的证据。术后MRI显示病变已完全切除,1年后停药月经恢复。