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囊性颗粒细胞瘤,类似 Rathke 裂隙囊肿。

Cystic granular cell tumor mimicking Rathke cleft cyst.

机构信息

Department of Neurosurgery, University of Utah, Salt Lake City, Utah 84132, USA.

出版信息

J Neurosurg. 2011 Feb;114(2):325-8. doi: 10.3171/2010.5.JNS1058. Epub 2010 May 28.

Abstract

Symptomatic granular cell tumors of the neurohypophysis are a rarely reported entity. To the authors' knowledge, they report the first fully described case of a symptomatic granular cell tumor with a large cystic component. A 31-year-old woman presented with headaches and visual complaints with imaging findings confirming a cystic sellar and suprasellar mass. The lesion was resected, and histological examination confirmed the diagnosis. The literature has shown that granular cell tumors are rarely reported as being symptomatic but may actually be a fairly common finding in autopsy studies. The authors review the literature with a specific focus on radiographic findings in patients with symptomatic granular cell tumors.

摘要

神经垂体有症状的颗粒细胞瘤是一种罕见的报道实体。据作者所知,他们报告了首例有大量囊性成分的有症状颗粒细胞瘤的完全描述性病例。一名 31 岁女性因头痛和视力问题就诊,影像学检查证实存在囊性蝶鞍和鞍上肿块。该病变被切除,组织学检查证实了诊断。文献表明,颗粒细胞瘤很少被报道为有症状,但实际上在尸检研究中可能是一种相当常见的发现。作者回顾了文献,特别关注有症状颗粒细胞瘤患者的影像学发现。

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