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进行性多灶性白质脑病的细胞学发现。两例报告。

Cytologic findings in progressive multifocal leukoencephalopathy. Report of two cases.

作者信息

Suhrland M J, Koslow M, Perchick A, Weiner E, Greco M A, Colquhoun F, Muller W D, Burstein D E

出版信息

Acta Cytol. 1987 Jul-Aug;31(4):505-11.

PMID:3604546
Abstract

Cytologic preparations from two cases of progressive multifocal leukoencephalopathy (PML) were obtained by stereotactically guided needle biopsies using computerized tomograms of the brain. Case 1 was a 32-year-old man with an acquired immunodeficiency syndrome-related complex. Case 2 was a 71-year-old man with chronic lymphocytic leukemia. Smears showed moderate cellularity, consisting of moderately to markedly atypical cells with enlarged hyperchromatic nuclei. The chromatin pattern showed smudging, with or without clumping, similar in pattern to the human polyomavirus-infected "decoy" cells seen in urine cytology. Nuclei were predominantly round to oval, smoothly contoured and often stripped of cytoplasm. Occasional bizarre lobulated or multinucleated forms were seen. Some atypical cells had abundant cytoplasm exhibiting stellate projections. Histologic sections of the biopsy material confirmed the diagnosis in each case. In both cases, electron microscopy demonstrated intranuclear polyoma-type virus particles. The present findings suggest that PML should be considered in the differential diagnosis of marked cytologic atypia in brain aspirates from immunocompromised patients.

摘要

通过立体定向引导针吸活检获取两例进行性多灶性白质脑病(PML)患者的细胞学标本,活检采用脑部计算机断层扫描。病例1为一名32岁患有获得性免疫缺陷综合征相关综合征的男性。病例2为一名71岁患有慢性淋巴细胞白血病的男性。涂片显示细胞数量中等,由中度至明显非典型细胞组成,细胞核增大、染色质增多。染色质模式呈现模糊,有或无聚集,与尿液细胞学中所见的人多瘤病毒感染的“诱饵”细胞模式相似。细胞核主要为圆形至椭圆形,轮廓光滑,且常无细胞质。偶尔可见怪异的分叶状或多核形式。一些非典型细胞有丰富的细胞质并呈现星状突起。活检材料的组织学切片在每个病例中均证实了诊断。在两例中,电子显微镜均显示核内多瘤病毒样颗粒。目前的发现提示,在免疫受损患者脑穿刺抽吸物中出现明显细胞学非典型性时,鉴别诊断应考虑进行性多灶性白质脑病。

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