首页> 外文期刊>Clinical neurology and neurosurgery >Progressive multifocal leukoencephalopathy developed in incomplete Heerfordt syndrome, a rare manifestation of sarcoidosis, without steroid therapy responding to cidofovir.
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Progressive multifocal leukoencephalopathy developed in incomplete Heerfordt syndrome, a rare manifestation of sarcoidosis, without steroid therapy responding to cidofovir.

机译:进行性多灶性白质脑病发展为不完全Heerfordt综合征,这是结节病的罕见表现,而对西多福韦没有类固醇治疗。

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摘要

Progressive multifocal leukoencephalopathy (PML) is a severe demyelinating disease of the central nervous system caused by the JC virus; the mortality rate is high and it is usually refractory to treatment. In non-HIV patients, PML occurs as a late consequence of hematologic malignancies or during prolonged immunosuppression for transplantation or autoimmune disease. We describe a 34-year-old PML patient with incomplete Heerfordt syndrome, a rare type of sarcoidosis, who had not received any immunosuppressants, including steroids, at the onset and who was clinically and radiologically responsive to the antiviral drug cidofovir.
机译:进行性多灶性白质脑病(PML)是由JC病毒引起的中枢神经系统严重脱髓鞘疾病;死亡率很高,通常难以治疗。在非HIV患者中,PML是血液系统恶性肿瘤的晚期结果,或者是在移植或自身免疫性疾病的长期免疫抑制期间发生。我们描述了一名不完全Heerfordt综合征的34岁PML患者,这是一种罕见的结节病类型,在发作时未接受任何免疫抑制剂(包括类固醇)治疗,并且对抗病毒药物西多福韦具有临床和放射学反应。

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