孤立性胸腔积液作为大b细胞淋巴瘤的表现:1例报告和诊断考虑。

IF 2.9 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY
Van Vlierberghe Magalie, Dewaide Rosina, Michaux Lucienne, Develter Wim, Van Aelst Sophie, Claerhout Helena
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引用次数: 0

摘要

背景:液体超载相关大b细胞淋巴瘤(FO-LBCL)是WHO第5版血淋巴样肿瘤分类中新增的一类。以前,这些病例被分类为原发性积液淋巴瘤样淋巴瘤(pel样(积液)淋巴瘤)或与hhv8无关的pel样淋巴瘤。随着知识的增长,这些实体的临床表现和预后的差异,需要一个明确的分类变得明显。方法:我们报告一位79岁男性患者,因大量胸腔积液而出现急性呼吸困难和咳嗽,并通过胸部CT扫描显示。进一步的PET-CT诊断评估显示除了胸腔积液外未发现肿瘤肿块。胸膜液细胞学检查显示大量大型非典型淋巴样细胞。流式细胞术免疫表型分析显示单克隆CD19+/CD20+ b细胞群优势,轻链限制和CD5表达。分子分析显示部分克隆性,细胞遗传学显示复杂的超二倍体核型。EBV原位杂交、HHV8和HIV检测均为阴性。未发现潜在的免疫缺陷或全身性疾病。结果和结论:基于这些发现,诊断与FO-LBCL最一致,但由于重叠的特征,与其他hhv8阴性积液型大b细胞淋巴瘤的区分仍然具有挑战性。患者接受了基于r - chop的免疫化疗,并保持临床稳定,无全身性进展。本病例强调了综合细胞学、免疫表型、分子和病毒学分析在建立基于积液的大b细胞淋巴瘤的正确分类中的关键作用,并强调了这一新兴实体带来的诊断挑战。准确识别FO-LBCL是必不可少的,因为它的临床行为和治疗意义不同于其他积液性淋巴瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolated Pleural Effusion as Presentation of a Large B-Cell Lymphoma: A Case Report and Diagnostic Considerations.

Background: Fluid Overload-associated Large B-Cell Lymphoma (FO-LBCL) is one of the newly added entities in the WHO classification of Haematolymphoid Tumors 5th edition [1]. Formerly, these cases were classified as primary effusion lymphoma-like (effusion) lymphoma (PEL-like (effusion) lymphoma) or HHV8-unrelated PEL-like lymphoma. As knowledge grew regarding the differences in clinical presentation and prognosis of these entities, the need for a distinct classification became apparent.

Method: We describe a case of a 79-year-old man with acute dyspnea and cough due to massive pleural effusion, revealed by CT scan of the thorax. Further diagnostic evaluation with PET-CT showed no detectable tumor mass apart from the pleural fluid. Pleural fluid cytology revealed numerous large atypical lymphoid cells. Flow cytometric immunophenotyping showed a predominant monoclonal CD19+/CD20+ B-cell population with light chain restriction and CD5 expression. Molecular analysis demonstrated partial clonality, and cytogenetics revealed a complex hyperdiploid karyotype. EBV in situ hybridization and testing for HHV8 and HIV were negative. No underlying immunodeficiency or systemic disease was identified.

Results and conclusion: Based on these findings, diagnosis was most consistent with FO-LBCL, but distinction from other HHV8-negative effusion-based large B-cell lymphomas remains challenging due to overlapping features. The patient received R-CHOP-based immunochemotherapy and remains clinically stable without systemic progression. This case highlights the critical role of integrated cytologic, immunophenotypic, molecular, and virological analyses in establishing the correct classification of effusion-based large B-cell lymphomas and underscores the diagnostic challenges posed by this emerging entity. Accurate recognition of FO-LBCL is essential, as its clinical behavior and therapeutic implications differ from other effusion-based lymphomas.

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来源期刊
Journal of Clinical Laboratory Analysis
Journal of Clinical Laboratory Analysis 医学-医学实验技术
CiteScore
5.60
自引率
7.40%
发文量
584
审稿时长
6-12 weeks
期刊介绍: Journal of Clinical Laboratory Analysis publishes original articles on newly developing modes of technology and laboratory assays, with emphasis on their application in current and future clinical laboratory testing. This includes reports from the following fields: immunochemistry and toxicology, hematology and hematopathology, immunopathology, molecular diagnostics, microbiology, genetic testing, immunohematology, and clinical chemistry.
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