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具有与蝶形胶质瘤相符临床特征的成人神经元蜡样脂褐质沉积症。病例报告。

Adult neuronal ceroid lipofuscinosis with clinical findings consistent with a butterfly glioma. Case report.

作者信息

Hammersen S, Brock M, Cervós-Navarro J

机构信息

Department of Neurosurgery and Institute of Neuropathology, Benjamin Franklin Medical Center, Free University of Berlin, Germany.

出版信息

J Neurosurg. 1998 Feb;88(2):314-8. doi: 10.3171/jns.1998.88.2.0314.

Abstract

The authors report a case of neuronal ceroid lipofuscinosis (Kufs' disease) confirmed by stereotactically obtained brain biopsy findings and initially diagnosed as a butterfly glioma. The presenting symptoms in the 64-year-old patient were mental alterations with progressive dementia, followed by muscular atrophy and myoclonia with distal preponderance. The mild initial disturbances of coordination increased, and the patient developed a markedly ataxic gait. Computerized tomography (CT) scanning and magnetic resonance imaging revealed generalized cerebral atrophy and a bifrontal space-occupying lesion involving the callosum. The original "clearcut" diagnosis of glioblastoma multiforme, based on CT scans, was unexpectedly disproved by examination of stereotactically obtained brain biopsy specimens, which revealed a neuronal ceroid lipofuscinosis (Kufs' disease). To the authors' knowledge, this is the first report of a case presenting with both diffuse brain atrophy and localized accumulation of neuronal lipofuscin, mimicking a mass lesion on radiological studies.

摘要

作者报告了一例经立体定向脑活检结果确诊为神经元蜡样脂褐质沉积症(库夫斯病)的病例,该病例最初被诊断为蝶形胶质瘤。这位64岁患者的首发症状是精神改变伴进行性痴呆,随后出现肌肉萎缩和以远端为主的肌阵挛。最初轻微的协调障碍加重,患者出现明显的共济失调步态。计算机断层扫描(CT)和磁共振成像显示全脑萎缩以及累及胼胝体的双额叶占位性病变。基于CT扫描最初“明确”诊断为多形性胶质母细胞瘤,但经立体定向脑活检标本检查意外地推翻了这一诊断,活检结果显示为神经元蜡样脂褐质沉积症(库夫斯病)。据作者所知,这是首例在影像学研究中表现为弥漫性脑萎缩和神经元脂褐质局部积聚、酷似肿块病变的病例报告。

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