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伴有黄色肉芽肿性改变的拉克氏裂囊肿——病例报告

Rathke's cleft cyst with xanthogranulomatous change--case report.

作者信息

Miyajima Yoshiteru, Oka Hidehiro, Utsuki Satoshi, Fujii Kiyotaka

机构信息

Department of Neurosurgery, Kitasato University School of Medicine, 1-15-1 Kitasato, Minami-ku, Sagamihara, Kanagawa, Japan.

出版信息

Neurol Med Chir (Tokyo). 2011;51(10):740-2. doi: 10.2176/nmc.51.740.

Abstract

A 58-year-old man presented with a rare case of Rathke's cleft cyst (RCC) manifesting as headache and visual disturbance. Goldman's perimeter showed he had bitemporal hemianopia. Magnetic resonance imaging revealed a solid intrasellar lesion. He underwent surgery via a right pterional approach. The lesion was red, solid, and fibrous. Histological examination revealed a few columnar epithelial cells with poor cilia in a xanthogranulomatous lesion. Only 13 cases of RCC with granulomatous change have been diagnosed by pathological examination, including 4 xanthogranulomatous cases. Xanthogranuloma of the sellar region is relatively rare. The etiology is still unknown. We speculate that xanthogranulomas of the sellar region may be caused by reaction to the presence of RCC.

摘要

一名58岁男性出现罕见的拉克氏裂囊肿(RCC),表现为头痛和视觉障碍。戈德曼视野计检查显示他患有双颞侧偏盲。磁共振成像显示鞍内有一个实性病变。他通过右翼点入路接受了手术。病变呈红色、实性且纤维状。组织学检查显示在一个黄色肉芽肿性病变中有一些柱状上皮细胞,纤毛较少。经病理检查确诊的伴有肉芽肿性改变的RCC仅有13例,其中黄色肉芽肿性病例4例。鞍区黄色肉芽肿相对罕见。病因仍不清楚。我们推测鞍区黄色肉芽肿可能是对RCC存在的反应所致。

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