Morphology and multiparameter flow cytometry combined for integrated lymphoma diagnosis on small volume samples: possibilities and limitations.

IF 3.4 3区 医学 Q1 PATHOLOGY Virchows Archiv Pub Date : 2024-10-01 Epub Date: 2024-05-28 DOI:10.1007/s00428-024-03819-3
Mats Ehinger, Marie C Béné
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Abstract

The diagnosis of lymphoma relies mainly on clinical examination and laboratory explorations. Among the latter, morphological and immunohistochemical analysis of a tissue biopsy are the cornerstones for proper identification and classification of the disease. In lymphoma with blood and/or bone marrow involvement, multiparameter flow cytometry is useful. This technique can also be applied to fresh cells released from a biopsy sample. For full comprehension of lymphomas, surgical biopsies are best and indeed recommended by the hematopathological community. Currently, however, there is a global trend towards less invasive procedures, resulting in smaller samples such as core needle biopsies or fine needle aspirations which can make the diagnosis quite challenging. In this review, the possibilities and limitations to make an accurate lymphoma diagnosis on such small volume material are presented. After recalling the major steps of lymphoma diagnosis, the respective value of histology, cytology, and flow cytometry is discussed, including handling of small specimens. The benefits of an integrated approach are then evoked, followed by discussion about which attitude to adopt in different contexts. Perhaps contrary to the prevailing view among many pathologists, a full diagnosis on small volume material, combined with relevant ancillary techniques, is often possible and indeed supported by recent literature. A glimpse at future evolutions, notably the merit of artificial intelligence tools, is finally provided. All in all, this document aims at providing pathologists with an overview of diagnostic possibilities in lymphoma patients when confronted with small volume material such as core needle biopsies or fine needle aspirations.

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结合形态学和多参数流式细胞术对小体积样本进行淋巴瘤综合诊断:可能性与局限性。
淋巴瘤的诊断主要依靠临床检查和实验室检测。其中,组织活检的形态学和免疫组化分析是正确识别和分类疾病的基石。对于累及血液和/或骨髓的淋巴瘤,多参数流式细胞术非常有用。这项技术也可用于活检样本中释放出的新鲜细胞。要全面了解淋巴瘤,最好进行手术活检,这也是血液病理学界所推荐的。然而,目前全球的趋势是采用创伤较小的手术方法,从而获得较小的样本,如芯针活检或细针抽吸,这可能使诊断变得相当具有挑战性。在这篇综述中,我们将介绍利用这种小体积样本准确诊断淋巴瘤的可能性和局限性。在回顾了淋巴瘤诊断的主要步骤后,讨论了组织学、细胞学和流式细胞术各自的价值,包括小标本的处理。然后唤起了综合方法的益处,接着讨论了在不同情况下应采取的态度。也许与许多病理学家的普遍观点相反,结合相关辅助技术对小样本材料进行全面诊断通常是可行的,最近的文献也确实支持这种观点。最后,我们还对未来的发展,尤其是人工智能工具的优点进行了展望。总之,本文件旨在向病理学家概述淋巴瘤患者面对核心针活检或细针抽吸等小体积材料时的诊断可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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