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干燥综合征患者并发进行性多灶性白质脑病和CD4+淋巴细胞减少症。

Progressive multifocal leukoencephalopathy and CD4+ T-lymphocytopenia in a patient with Sjögren syndrome.

作者信息

Hayashi Yuichi, Kimura Akio, Kato Shimon, Koumura Akihiro, Sakurai Takeo, Tanaka Yuji, Hozumi Isao, Sunden Yuji, Orba Yasuko, Sawa Hirofumi, Takahashi Hitoshi, Inuzuka Takashi

机构信息

Department of Neurology and Geriatrics, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu, Gifu 501-1194, Japan.

出版信息

J Neurol Sci. 2008 May 15;268(1-2):195-8. doi: 10.1016/j.jns.2007.12.015. Epub 2008 Jan 29.

Abstract

We report progressive multifocal leukoencephalopathy (PML) and CD4+ T-lymphocytopenia in a 71-year-old man with Sjögren syndrome (SjS). The patient was admitted to our hospital because of progressive dementia and gait disturbance. T2-weighted MR images showed high-intensity lesions in his left frontal white matter thalamus, cerebellum and brainstem. A pathological diagnosis of PML was made by brain biopsy. SjS is frequently accompanied with immunological complications; however, there are few reports on PML in patients with SjS. Recently, isolated CD4+ T-lymphocytopenia is reported to be one of the based immunological conditions associated with the development of PML. In the present case, CD4+ T-lymphocytopenia was also observed on admission, which is also associated with SjS.

摘要

我们报告了一名71岁干燥综合征(SjS)男性患者出现进行性多灶性白质脑病(PML)和CD4 + T淋巴细胞减少症。该患者因进行性痴呆和步态障碍入院。T2加权磁共振成像显示其左额叶白质、丘脑、小脑和脑干有高强度病变。通过脑活检做出了PML的病理诊断。SjS常伴有免疫并发症;然而,关于SjS患者发生PML的报道很少。最近,有报道称孤立性CD4 + T淋巴细胞减少症是与PML发生相关的基础免疫状况之一。在本病例中,入院时也观察到了CD4 + T淋巴细胞减少症,这也与SjS有关。

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