Progressive multifocal encephalopathy after cyclophosphamide in granulomatosis with polyangiitis (Wegener) patients: case report and review of the literature

被引:0
作者
Pugnet, G. [1 ]
Pagnoux, C. [2 ]
Bezanahary, H. [3 ]
Ly, K. H. [3 ]
Vidal, E. [3 ]
Guillevin, L. [2 ]
机构
[1] CHU Toulouse Purpan, Serv Med Interne Salle Le Tallec, F-31059 Toulouse, France
[2] Hop Cochin, Serv Med Interne, Ctr Reference Malad Syst Autoimmunes Rares, F-75674 Paris, France
[3] CHU Dupuytren, Serv Med Interne A, Limoges, France
关键词
progressive multifocal encephalopathy; granulomatosis with polyangiitis; (Wegener); cyclophosphamide; LEUKOENCEPHALOPATHY; RITUXIMAB;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Progressive multifocal encephalopathy (PML) is a rare demyelinating disorder targeting the central nervous system and resulting from JC virus reactivation. PML occurs in patients imrnunocompromised because of haematological malignancies, HIV infection or treatment with cytotoxic drugs. Herein, we describe PML occurring in 2 granulomatosis with polyangiitis (Wegener) patients treated with steroids and cyclophosphamide. The outcome was progressively favourable after immunosuppressant discontinuation for 1 patient and fatal for the other. Four previously reported GPA patients developed PML in the course of their disease. One of them improved gradually after immunosuppressant withdrawal. PML - should be strongly suspected whenever unusual central neurological manifestations appear in this context. No effective treatment is available, but immunosuppressants should be discontinued if possible.
引用
收藏
页码:S62 / S64
页数:3
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