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进行性多灶性白质脑病并发系统性红斑狼疮。

Progressive multifocal leukoencephalopathy complicating systemic lupus erythematosus.

作者信息

Newton P, Aldridge R D, Lessells A M, Best P V

出版信息

Arthritis Rheum. 1986 Mar;29(3):337-43. doi: 10.1002/art.1780290305.

Abstract

Two patients with systemic lupus erythematosus who developed progressive multifocal leukoencephalopathy (PML) are described. Although the time of PML onset could not be determined with certainty, it probably developed after steroid-induced immunosuppression. However, high-dose corticosteroids appeared to produce transient amelioration in the neurologic disorder. We suggest that PML is an important addition to the list of conditions to be considered in the differential diagnosis when a patient with systemic lupus erythematosus develops neurologic abnormalities.

摘要

本文描述了两名患有系统性红斑狼疮并发生进行性多灶性白质脑病(PML)的患者。虽然PML的发病时间无法确切确定,但很可能是在类固醇诱导的免疫抑制后发生的。然而,高剂量皮质类固醇似乎使神经功能障碍出现了短暂改善。我们认为,当系统性红斑狼疮患者出现神经异常时,PML是鉴别诊断中需要考虑的重要疾病之一。

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