Institute of Pathology, University of Würzburg, Josef-Schneider-Str. 2, 97080, Würzburg, Germany.
Pathology-DNA, Location Rijnstate Hospital, Wagnerlaan 55, 6815AD, Arnhem, The Netherlands.
Virchows Arch. 2023 Sep;483(3):317-331. doi: 10.1007/s00428-023-03633-3. Epub 2023 Sep 1.
Session 3 of the lymphoma workshop of the XXI joint meeting of the European Association for Haematopathology and the Society for Hematopathology took place in Florence, Italy, on September 22, 2022. The topics of this session were splenic and nodal marginal zone lymphomas, transformation in marginal zone lymphomas, and pediatric nodal marginal zone lymphomas and their differential diagnosis as well as related entities. Forty-two cases in these categories were submitted to the workshop, including splenic lymphomas (marginal zone and diffuse red pulp lymphomas), transformed marginal zone lymphomas (splenic and nodal), nodal marginal zone lymphomas with increased TFH-cells, and pediatric nodal marginal zone lymphomas. The case review highlighted some of the principal problems in the diagnosis of marginal zone lymphomas, including the difficulties in the distinction between splenic marginal zone lymphoma, splenic diffuse red pulp lymphoma, and hairy cell leukemia variant/splenic B-cell lymphoma with prominent nucleoli which requires integration of clinical features, immunophenotype, and morphology in blood, bone marrow, and spleen; cases of marginal zone lymphoma with markedly increased TFH-cells, simulating a T-cell lymphoma, where molecular studies (clonality and mutation detection) can help to establish the final diagnosis; the criteria for transformation of marginal zone lymphomas, which are still unclear and might require the integration of morphological and molecular data; the concept of an overlapping spectrum between pediatric nodal marginal zone lymphoma and pediatric-type follicular lymphoma; and the distinction between pediatric nodal marginal zone lymphoma and "atypical" marginal zone hyperplasia, where molecular studies are mandatory to correctly classify cases.
XXI 届欧洲血液病理学协会和血液病理学学会联合会议的淋巴瘤研讨会第 3 场于 2022 年 9 月 22 日在意大利佛罗伦萨举行。本次会议的主题是脾脏和淋巴结边缘区淋巴瘤、边缘区淋巴瘤的转化、儿科淋巴结边缘区淋巴瘤及其鉴别诊断以及相关实体。该研讨会提交了 42 例此类病例,包括脾脏淋巴瘤(边缘区和弥漫性红髓淋巴瘤)、转化边缘区淋巴瘤(脾脏和淋巴结)、TFH 细胞增多的淋巴结边缘区淋巴瘤和儿科淋巴结边缘区淋巴瘤。病例回顾强调了边缘区淋巴瘤诊断中的一些主要问题,包括在区分脾脏边缘区淋巴瘤、脾脏弥漫性红髓淋巴瘤和毛细胞白血病变异/具有显著核仁的脾脏 B 细胞淋巴瘤时存在困难,这需要整合临床特征、免疫表型和血液、骨髓和脾脏中的形态学;TFH 细胞显著增加的边缘区淋巴瘤病例,模拟 T 细胞淋巴瘤,其中分子研究(克隆性和突变检测)有助于确立最终诊断;边缘区淋巴瘤转化的标准仍不清楚,可能需要整合形态学和分子数据;儿科淋巴结边缘区淋巴瘤和儿科型滤泡淋巴瘤之间存在重叠谱的概念;以及儿科淋巴结边缘区淋巴瘤和“非典型”边缘区增生之间的区别,其中分子研究是正确分类病例的必要条件。