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合并韦格纳肉芽肿的JC病毒白质脑病

JC virus leukoencephalopathy complicating Wegener's granulomatosis.

作者信息

Pagnoux Christian, Hayem Gilles, Roux Fabienne, Rouidi Sid Ahmed, Palazzo Elizabeth, Hénin Dominique, Meyer Olivier

机构信息

Travail du Service de Rhumatologie, Groupe Hospitalier Bichat-Claude-Bernard, 46, rue Henri-Huchard, 75877 Paris cedex 18, France.

出版信息

Joint Bone Spine. 2003 Sep;70(5):376-9. doi: 10.1016/s1297-319x(03)00062-9.

Abstract

Progressive multifocal leukoencephalopathy (PML) is a demyelinating disease of the brain caused by the JC virus. It occurs in association with immunodepression due, for instance, to a hematological malignancy, HIV infection, or immunosuppressive therapy for an organ transplant or systemic disease. We describe the fourth reported case of PML in a patient receiving immunosuppressants for Wegener's granulomatosis. A 71-year-old woman receiving azathioprine and glucocorticoid therapy experienced onset of right-sided hemiplegia within a few days, became comatose, and died within a few days. MRI of the brain showed a subcortical lesion in the left parietal lobe generating low signal on T1 images and high signal on T2 images. The initial diagnosis was cerebral vasculitis. However, the postmortem examination showed PML. The diagnosis of PML rests on JC virus detection in the cerebrospinal fluid by PCR assay and on demonstration in a brain biopsy of the typical histological pattern with presence of the JC virus within the demyelinated lesions. No specific or effective treatments are available. Immunosuppressant drugs should be discontinued if possible.

摘要

进行性多灶性白质脑病(PML)是一种由JC病毒引起的脑部脱髓鞘疾病。它常与免疫抑制相关,例如因血液系统恶性肿瘤、HIV感染,或因器官移植或全身性疾病而接受免疫抑制治疗。我们报告了第四例因韦格纳肉芽肿接受免疫抑制剂治疗而发生PML的病例。一名71岁女性接受硫唑嘌呤和糖皮质激素治疗,数天内出现右侧偏瘫,陷入昏迷,并在数天内死亡。脑部MRI显示左顶叶皮质下病变,在T1图像上呈低信号,在T2图像上呈高信号。初步诊断为脑血管炎。然而,尸检显示为PML。PML的诊断基于通过PCR检测脑脊液中的JC病毒,以及在脑活检中显示典型的组织学模式且脱髓鞘病变内存在JC病毒。目前尚无特异性或有效的治疗方法。如有可能,应停用免疫抑制药物。

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