首页> 美国卫生研究院文献>The Journal of Neurology and Psychopathology >An unusual course of progressive multifocal leukoencephalopathyin a patient with idiopathic CD4+ T lymphocytopenia
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An unusual course of progressive multifocal leukoencephalopathyin a patient with idiopathic CD4+ T lymphocytopenia

机译:进行性多灶性白质脑病的不寻常病程特发性CD4 + T淋巴细胞减少的患者

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摘要

A case is reported of idiopathic CD4+T lymphocytopenia with progressive multifocal leukoencephalopathy and cervical lymph node tuberculosis. A 57 year old Japanese man presented with cervical lymphadenopathy and progressive neurological deficits, and six months later he developed akinetic mutism. He had a persistent severely depressed number of circulating CD4+T lymphocytes in the absence of human immunodeficiency virus infection. T1 weighted MRI showed a diffuse decreased signal intensity limited to the white matter without mass effect. A brain biopsy specimen had a morphology similar to that of progressive multifocal leukoencephalopathy. Polyomavirus antigen was detected in the brain lesion, and viral DNA was identified in nucleated blood cells and urine. Unusually this serious medical condition has lasted for more than three years without remission. To our knowledge this is the first patient with CD4+T lymphocytopenia with progressive multifocal leukoencephalopathy, suggesting that similar opportunistic infections should be considered even in previously normal people.

机译:报道了一例特发性CD4 + T淋巴细胞减少症,伴进行性多灶性白质脑病和颈淋巴结结核。一名57岁的日本男子患有颈淋巴结肿大和进行性神经功能缺损,六个月后出现了运动性kin默症。在没有人类免疫缺陷病毒感染的情况下,他的循环CD4 + T淋巴细胞数量持续严重降低。 T1加权MRI显示仅限于白质的弥散性降低信号强度,无质量效应。脑活检标本的形态与进行性多灶性白质脑病相似。在脑病变中检测到多瘤病毒抗原,并在有核血细胞和尿液中鉴定出病毒DNA。异常的这种严重的疾病状况持续了三年多,没有缓解。据我们所知,这是首例患有进行性多灶性白质脑病的CD4 + T淋巴细胞减少的患者,这表明即使在以前的正常人群中也应考虑类似的机会性感染。

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