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伯氏疏螺旋体相关皮肤淋巴细胞瘤:106例临床病理、免疫表型及分子研究

Borrelia burgdorferi-associated lymphocytoma cutis: clinicopathologic, immunophenotypic, and molecular study of 106 cases.

作者信息

Colli Claudia, Leinweber Bernd, Müllegger Robert, Chott Andreas, Kerl Helmut, Cerroni Lorenzo

机构信息

Department of Dermatology, University of Graz, Austria.

出版信息

J Cutan Pathol. 2004 Mar;31(3):232-40. doi: 10.1111/j.0303-6987.2003.00167.x.

Abstract

Lymphocytoma cutis (LC) is considered as the stereotypical example of the cutaneous B-cell pseudolymphomas. It can be induced by various antigenic stimuli including arthropod bites, vaccination, and drugs among others. In endemic regions, Borrelia burgdorferi is the principal causative agent for LC. We studied retrospectively 108 biopsies from 106 patients (male : female, 48 : 58; mean age, 44.6; median, 51.5; range, 3-81) with B. burgdorferi-associated LC retrieved from the files of the Department of Dermatology of the University of Graz (Austria). Only cases with a B. burgdorferi etiology (typical locations, positivity of serologic and/or polymerase chain reaction (PCR) tests, clinical history) were included in the study. Lesions were located on the nipple (63 cases), earlobe (18 cases), genital region (9 cases), and trunk or extremities (16 cases). PCR analysis of B. burgdorferi DNA was positive in 54 of 80 cases tested (67.5%). In 47 cases, we could retrieve data on serologic examination for B. burgdorferi antibodies performed at the time of diagnosis of LC. Positivity was found in 45 patients (IgG+/IgM+, 5 cases; IgG+/IgM-, 37 cases; IgG-/IgM+, 3 cases; IgG-/IgM-, 2 cases). Histology revealed dense lymphoid infiltrates with prominent germinal centers (GCs) in all cases. Atypical morphologic and/or immunophenotypic features of the GCs were commonly observed. In 5 cases, due to confluence of large follicles, the histopathologic pattern simulated that of a large B-cell lymphoma. PCR analysis of the IgH gene rearrangement performed in 33 cases showed a polyclonal pattern in 31 cases and a monoclonal band in 2. In summary, B. burgdorferi-associated LC can present with misleading histopathologic, immunophenotypic, and molecular features, and integration of all data is necessary for a correct diagnosis.

摘要

皮肤淋巴细胞瘤(LC)被认为是皮肤B细胞假性淋巴瘤的典型例子。它可由多种抗原刺激诱发,包括节肢动物叮咬、接种疫苗和药物等。在流行地区,伯氏疏螺旋体是LC的主要致病因子。我们回顾性研究了从奥地利格拉茨大学皮肤科档案中检索到的106例患者(男∶女,48∶58;平均年龄44.6岁,中位数51.5岁,范围3 - 81岁)的108份与伯氏疏螺旋体相关的LC活检标本。本研究仅纳入具有伯氏疏螺旋体病因(典型部位、血清学和/或聚合酶链反应(PCR)检测阳性、临床病史)的病例。病变位于乳头(63例)、耳垂(18例)、生殖器区域(9例)以及躯干或四肢(16例)。在80例检测病例中,54例(67.5%)伯氏疏螺旋体DNA的PCR分析呈阳性。在47例病例中,我们能够获取LC诊断时进行的伯氏疏螺旋体抗体血清学检查数据。45例患者呈阳性(IgG + /IgM +,5例;IgG + /IgM -,37例;IgG - /IgM +,3例;IgG - /IgM -,2例)。组织学检查显示所有病例均有密集的淋巴样浸润伴明显的生发中心(GCs)。常见观察到GCs的非典型形态学和/或免疫表型特征。5例病例中,由于大滤泡融合,组织病理学模式类似大B细胞淋巴瘤。对33例病例进行的IgH基因重排PCR分析显示,31例为多克隆模式,2例为单克隆条带。总之,与伯氏疏螺旋体相关的LC可呈现出具有误导性的组织病理学、免疫表型和分子特征,综合所有数据对于正确诊断是必要的。

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