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Lymphoma classification and the tools of our trade: an introduction to the 2012 USCAP Long Course

机译:淋巴瘤的分类和我们的交易工具:2012年USCAP长期课程简介

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The 2012 USCAP Long Course ‘Malignant Lymphomas—Building on the Past, Moving to the Future’ began with an introduction to lymphoma classification over the last half century and a discussion of our current diagnostic armamentarium, together with a look toward the future. The Rappaport classification, originally published in 1956, was a morphologic classification with few categories. The early 1970s saw a great and tumultuous revolution in the field with the publication of two functional lymphoma classifications that related the malignant lymphomas to the cells of the normal immune system—the Lukes/Collins classification from the United States and the Kiel classification from Professor Lennert and the European Lymphoma Club. With discord abounding, the NCI working formulation, published in 1982, satisfied some but was a step back to a morphologic-based classification. In 1994, the International Lymphoma Study Group published the REAL classification, which reflected state-of-the-art practice for that time, and was shortly followed by preparations for the modern World Health Organization (WHO) classification published in 2001 and revised in 2008. The WHO classification, created by hematopathologists working with the advice and consent of clinical hematologist/oncologists, recognizes numerous distinct entities, defined based on their histopathological, immunophenotypical, molecular/cytogenetic and clinical features. The classification requires use of a multiparameter approach to lymphoma diagnosis although we still rely heavily on histopathology. Immunophenotypical studies, whether using paraffin section immunohistochemistry and/or flow cytometry, are also critical in almost all circumstances. Molecular/cytogenetic techniques that are constantly changing have an increasingly important role, even if not always required. The full impact of next-generation sequencing is yet to be felt but we are beginning to catch a glimpse of what is in our future. Finally, one must not forget the great importance of clinical data in arriving at a diagnosis that best serves the patient, our ultimate goal.
机译:2012年的USCAP长期课程“恶性淋巴瘤-过去的基础上,走向未来”首先介绍了过去半个世纪的淋巴瘤分类,并讨论了我们目前的诊断性武器库以及对未来的展望。 Rappaport分类最初发布于1956年,是形态分类很少的分类。 1970年代初,随着两个功能性淋巴瘤分类的发表,该领域发生了巨大而动荡的革命,这两种分类将恶性淋巴瘤与正常免疫系统的细胞联系在一起-美国的Lukes / Collins分类和Lennert教授的Kiel分类。和欧洲淋巴瘤俱乐部。面对纷争不一的情况,1982年出版的NCI工作方案满足了一些要求,但又退回到了基于形态学的分类标准。 1994年,国际淋巴瘤研究小组发布了REAL类别,该类别反映了当时的最新实践,随后不久便为2001年发布并于2008年修订的现代世界卫生组织(WHO)分类做准备。由血液病理学家在临床血液学家/肿瘤学家的建议和同意下创建的WHO分类标准,可识别许多不同的实体,这些实体是根据其组织病理学,免疫表型,分子/细胞遗传学和临床特征定义的。尽管我们仍然严重依赖组织病理学,但分类需要使用多参数方法来诊断淋巴瘤。在几乎所有情况下,是否使用石蜡切片免疫组织化学和/或流式细胞术进行免疫表型研究都是至关重要的。即使不总是需要,不断变化的分子/细胞遗传学技术也发挥着越来越重要的作用。下一代测序的全部影响尚待观察,但是我们开始瞥见我们的未来。最后,一定不要忘记临床数据在做出最能为患者服务的诊断中的重要性,这是我们的最终目标。

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