Yu G H, Hidvegi D F, Cajulis R S, Brody B A, Levy R M
Department of Pathology, Northwestern University Medical School, Chicago, IL 60611, USA.
Diagn Cytopathol. 1996 Feb;14(1):4-9. doi: 10.1002/(SICI)1097-0339(199602)14:1<4::AID-DC2>3.0.CO;2-L.
Progressive multifocal leukoencephalopathy (PML) is a fatal demyelinating disorder of the central nervous system (CNS) resulting from infection of oligodendrocytes by JC virus. Although all patients immunocompromised by any congenital, acquired, or iatrogenic condition are at risk, the population which currently accounts for the majority of new cases is that infected with the human immunodeficiency virus (HIV). Though the clinical/radiologic presentation is characteristic, biopsy confirmation is necessary, as these patients are at risk for other primary CNS disorders which may produce similar clinical findings. Immediate assessment of tissue adequacy by cytologic smear is generally preferred in these specimens due to its relative reduced risk of disease transmission when compared to conventional frozen section. We report here the cytologic findings seen in touch imprints and squash preparations of 16 cases of PML, all occurring in HIV-positive patients and obtained by stereotactic guided needle biopsy. Typical cytomorphologic findings are described and correlated with histologic sections. In addition, features useful in the exclusion of other differential diagnostic possibilities are discussed.
进行性多灶性白质脑病(PML)是一种由JC病毒感染少突胶质细胞引起的致命性中枢神经系统脱髓鞘疾病。尽管所有因任何先天性、后天性或医源性疾病导致免疫功能低下的患者都有患病风险,但目前新发病例的大多数人群是感染了人类免疫缺陷病毒(HIV)的患者。虽然临床/影像学表现具有特征性,但活检确诊是必要的,因为这些患者有患其他可能产生类似临床症状的原发性中枢神经系统疾病的风险。由于与传统冰冻切片相比,其疾病传播风险相对降低,因此在这些标本中,通过细胞学涂片立即评估组织是否充足通常是首选方法。我们在此报告16例PML患者在触片和压片标本中的细胞学发现,所有病例均发生在HIV阳性患者中,且通过立体定向引导针吸活检获取。描述了典型的细胞形态学发现,并与组织学切片进行了相关性分析。此外,还讨论了有助于排除其他鉴别诊断可能性的特征。