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通过小脑活检生前诊断的原发性小脑桥脑进行性多灶性白质脑病。

Primary cerebellopontine progressive multifocal leukoencephalopathy diagnosed premortem by cerebellar biopsy.

作者信息

Jones H R, Hedley-Whyte E T, Freidberg S R, Kelleher J E, Krolikowski J

出版信息

Ann Neurol. 1982 Feb;11(2):199-202. doi: 10.1002/ana.410110218.

DOI:10.1002/ana.410110218
PMID:7073254
Abstract

A subacute progressive cerebellar brainstem syndrome developed in a patient with systemic lupus erythematosus in remission. Cerebellar biopsy documented the diagnosis of progressive multifocal leukoencephalopathy (PML). Data from this patient and 10 others in the literature emphasize the need to consider this diagnosis when ataxia develops in any patient with underlying malignancy, chronic infection, or other disease that involves immunological incompetence. Although the ataxic form of PML is not of nosological relevance, early diagnosis may eventually have therapeutic importance.

摘要

一名处于缓解期的系统性红斑狼疮患者出现了亚急性进行性小脑脑干综合征。小脑活检确诊为进行性多灶性白质脑病(PML)。该患者及文献中其他10例患者的数据强调,任何患有潜在恶性肿瘤、慢性感染或其他涉及免疫功能不全疾病的患者出现共济失调时,都需要考虑这一诊断。尽管PML的共济失调形式与疾病分类无关,但早期诊断最终可能具有治疗意义。

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