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Progressive Multifocal Leukoencephalopathy Localized in the Cerebellum and Brainstem Associated with Idiopathic CD4(+) T Lymphocytopenia

机译:进行性多灶性白质脑病定位于特发性CD4(+)T淋巴细胞减少症相关的小脑和脑干

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摘要

Progressive multifocal leukoencephalopathy (PML) is a demyelinating disease that favors the cerebrum and typically occurs in immunosuppressed patients. We herein report the case of a 66-year-old man with PML, idiopathic CD4(+) T lymphocytopenia (ICL), and chronic renal failure. Cranial magnetic resonance imaging (MRI) showed a crescent-shaped lesion in the left cerebellum, brainstem, and middle cerebellar peduncle. Although the patient did not present with HIV infection, collagen diseases, or tumors, JC virus DNA was detected in the cerebrospinal fluid. Clinicians should consider PML and ICL in the differential diagnosis if the patient develops progressive ataxia and a crescent-shaped cerebellar lesion on MRI.
机译:进行性多灶性白质脑病(PML)是一种脱髓鞘疾病,有利于大脑,通常发生在免疫抑制的患者中。我们在此报告了66岁的PML,特发性CD4(+)T淋巴细胞减少症(ICL)和慢性肾功能衰竭的男人的情况。颅脑磁共振成像(MRI)显示左小脑,脑干和小脑中轴有新月形病变。尽管患者未出现HIV感染,胶原蛋白疾病或肿瘤,但在脑脊液中检测到JC病毒DNA。如果患者在进行性共济失调和MRI上出现新月形小脑病变,临床医生应在鉴别诊断中考虑PML和ICL。

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