Kurisaka M, Fukui N, Sakamoto T, Mori K, Okada T, Sogabe K
Department of Neurosurgery, Kochi Medical School, Nankoku-city, Japan.
Childs Nerv Syst. 1998 Jul;14(7):343-7. doi: 10.1007/s003810050240.
We report a case of Rathke's cleft cyst associated with cholesterin granuloma in an 8-year-old girl with apoplexy. She was admitted to our hospital in April 1996 because of repeated headache and deep ophthalmic pain, without any visual disturbance. Computed tomography (CT) of the pituitary demonstrated an intrasellar isodense mass extending to the suprasellar cistern. Magnetic resonance imaging (MRI) showed a high-intensity mass on both T1- and T2-weighted images. The preoperative diagnosis of this lesion was Rathke's cleft cyst associated with a craniopharyngioma and/or hemorrhage. Transsphenoidal microsurgery was performed, and a bloody coffee-like serous and mucinous-yellowish substance was evacuated. Curettage of the wall removed the yellowish hard mass and soft membranous tissue. Histological examination of this tumor revealed a Rathke's cleft cyst with cholesterin granuloma.
我们报告一例8岁患卒中的女孩,其患有与胆固醇肉芽肿相关的拉克氏裂囊肿。她因反复头痛和深部眼痛于1996年4月入住我院,无任何视力障碍。垂体计算机断层扫描(CT)显示鞍内等密度肿块延伸至鞍上池。磁共振成像(MRI)在T1加权和T2加权图像上均显示为高强度肿块。该病变的术前诊断为与颅咽管瘤和/或出血相关的拉克氏裂囊肿。进行了经蝶窦显微手术,抽出了血性咖啡样浆液性和粘液性淡黄色物质。刮除囊肿壁去除了淡黄色硬块和软膜样组织。该肿瘤的组织学检查显示为伴有胆固醇肉芽肿的拉克氏裂囊肿。