Nowak-Michalska T, Barcikowska M, Kida E, Budka H, Liberski P P
Kliniki Neurologicznej II Wydz. Lek. AM, Warszawie.
Neurol Neurochir Pol. 1993 Nov-Dec;27(6):905-12.
We report here a case of PML in the course of untreated chronic lymphocytic leukaemia. The diagnosis of PML was based on the presence of typical histologic findings in the white matter: focal demyelination, abnormal oligodendroglia with basophilic intranuclear inclusions and enlarged bizarre astrocytes. It was confirmed by immunohistochemistry which revealed JC papova-virus antigens in brain tissue and by in-situ hybridization which showed JC virus genomic DNA in oligodendroglial nuclei. Virus particles in the nuclei of abnormal oligodendrocytes and astrocytes were demonstrated by thin-section electron-microscopy.
我们在此报告一例未经治疗的慢性淋巴细胞白血病病程中发生进行性多灶性白质脑病(PML)的病例。PML的诊断基于白质中典型的组织学表现:局灶性脱髓鞘、伴有嗜碱性核内包涵体的异常少突胶质细胞以及肿大的怪异星形胶质细胞。免疫组化显示脑组织中有JC多瘤病毒抗原,原位杂交显示少突胶质细胞核中有JC病毒基因组DNA,从而得以确诊。超薄切片电子显微镜证实异常少突胶质细胞和星形胶质细胞核中有病毒颗粒。