Department of Pathology, Ohio State University Wexner Medical Center, Columbus, Ohio.
Cancer Cytopathol. 2018 Aug;126 Suppl 8:615-626. doi: 10.1002/cncy.22013.
Ancillary testing is absolutely integral to the correct recognition and classification of lymphoid neoplasms as procured with the fine-needle aspiration (FNA) biopsy technique. In patients with a newly diagnosed lymphoid neoplasm, immunophenotyping with flow cytometry, immunohistochemistry, or both is a standard that is currently expected by oncologists before any form of therapy is initiated. This is often the case also for patients with recurrent/relapsed disease. The cellular material obtained with FNA is perfectly suited to meet this demand. That said, the exceptional complexity of modern-day lymphoma classification often precludes definitive subclassification in a subset of lymphomas for a variety of reasons with the FNA biopsy technique, even with the application of ancillary tests. These include a requirement for definitive knowledge of the nodal architecture (eg, Hodgkin lymphoma), of the histologic grade via the counting of cells per microscopic field (follicular lymphoma), and of molecular findings (often unobtainable because of limitations of cellularity). The application of molecular tests to lymph node aspirates continues to evolve but is still largely confined to specialized medical centers. The intent of this article is to briefly review the diagnostic approach and algorithm for handling lymph node aspirates at the authors' own laboratory. This article highlights what the authors and others consider to be essential ancillary tests and discusses their respective advantages and shortcomings. It lists limited and extended antibody panels and molecular tests that the authors have found helpful not only for correctly recognizing lymphoma with FNA cytopathology but also for subtyping lymphomas whenever possible.
辅助检测对于正确识别和分类淋巴肿瘤至关重要,这些肿瘤是通过细针抽吸(FNA)活检技术获得的。对于新诊断出的淋巴肿瘤患者,流式细胞术、免疫组织化学或两者联合的免疫表型检测是目前肿瘤学家在开始任何形式的治疗之前所期望的标准。对于复发性疾病患者也是如此。FNA 获得的细胞材料非常适合满足这一需求。也就是说,由于各种原因,即使应用了辅助检测,现代淋巴瘤分类的异常复杂性通常也排除了 FNA 活检技术对某些淋巴瘤进行明确亚分类的可能性。这些原因包括对淋巴结结构(例如霍奇金淋巴瘤)的明确了解、通过每个显微镜视野的细胞计数来确定组织学分级(滤泡性淋巴瘤)以及分子发现(由于细胞数量的限制,通常无法获得)的要求。分子检测在淋巴结抽吸物中的应用仍在不断发展,但仍主要局限于专门的医疗中心。本文的目的是简要回顾作者所在实验室处理淋巴结抽吸物的诊断方法和算法。本文重点介绍了作者和其他人认为是必要的辅助检测,并讨论了它们各自的优缺点。它列出了作者发现有助于不仅通过 FNA 细胞学正确识别淋巴瘤,而且尽可能对淋巴瘤进行亚型分类的有限和扩展抗体面板和分子检测。