一份通过脑脊液细胞学诊断出的原发性中枢神经系统淋巴瘤病例报告，该病伴有免疫缺陷/紊乱。

IF 1.2 4区医学 Q4 CELL BIOLOGY

Cytopathology Pub Date : 2024-08-09 DOI:10.1111/cyt.13434

Jinnan Li, Xueqin Deng, Sha Zhao, Xueying Su

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引用次数: 0

摘要

在免疫缺陷/失调情况下发生的原发性中枢神经系统淋巴瘤（IDD-PCNSL）的脑脊液（CSF）细胞学检查尚未见报道。本研究介绍了一例IDD-PCNSL-DLBCL病例，该病例为GCB表型，通过脑脊液细胞学结合ICC、ISH、FCM和临床信息成功确诊。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

A case report of primary central nervous system lymphoma with immune deficiency/disorder setting diagnosed by cerebrospinal fluid cytology

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A case report of primary central nervous system lymphoma with immune deficiency/disorder setting diagnosed by cerebrospinal fluid cytology

Cerebrospinal fluid (CSF) cytology of primary central nervous system lymphoma arising in the immune deficiency/dysregulation setting (IDD-PCNSL) has not been described. This study presented a case of IDD-PCNSL-DLBCL, a GCB phenotype who was successfully diagnosed by CSF cytology in conjunction with ICC, ISH, FCM and clinical information.

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来源期刊

Cytopathology 生物-病理学

CiteScore

2.30

自引率

15.40%

发文量

107

审稿时长

6-12 weeks

期刊介绍： The aim of Cytopathology is to publish articles relating to those aspects of cytology which will increase our knowledge and understanding of the aetiology, diagnosis and management of human disease. It contains original articles and critical reviews on all aspects of clinical cytology in its broadest sense, including: gynaecological and non-gynaecological cytology; fine needle aspiration and screening strategy. Cytopathology welcomes papers and articles on: ultrastructural, histochemical and immunocytochemical studies of the cell; quantitative cytology and DNA hybridization as applied to cytological material.