Anatomic Pathology Service and Translational Hematopathology Lab, Hospital Universitario Marques de Valdecilla/IDIVAL, Santander, Spain.
Division of Hematopathology, Mayo Clinic, Rochester, MN, USA.
Virchows Arch. 2020 May;476(5):667-681. doi: 10.1007/s00428-019-02704-8. Epub 2019 Nov 26.
This paper summarizes two sessions of the workshop during the XIX meeting of the European Association for Haematopathology (EAHP) held in Edinburgh in September 2018 dedicated to lymphomas of the gastrointestinal tract. The first session focused on the clinical and pathological features of primary gastrointestinal T cell and NK-cell lymphoproliferative disorders. The distinction between precursor lesions (RCD type 2) and enteropathy-associated T cell lymphoma were stressed, including the discussion of new diagnostic markers for the identification of aberrant phenotypes. Indolent T cell lymphoproliferative disorders of the gastrointestinal tract cases showed phenotypic heterogeneity with novel molecular alterations in few cases, such as STAT3-JAK2 fusion. In addition, novel clonal markers of disease, such as AXL and JAK3 somatic variants support the neoplastic nature of NK-cell enteropathy. The session on gastrointestinal tract B cell lymphoproliferations was dedicated to B cell lymphoproliferative disorders that arise primarily in the gastrointestinal tract (i.e., duodenal-type follicular lymphoma) or preferentially involve the digestive tract, such as large B cell lymphoma with IRF4 translocation and mantle cell lymphoma (MCL), including diverse molecular subtypes (i.e., CCND3-positive MCL mimicking MALT lymphoma). Challenging cases of high-grade B cell lymphomas with complex genetic profiles demonstrated the usefulness of novel molecular diagnostic methods such as targeted NGS to identify high-risk genetic features with potential clinical impact.
本文总结了 2018 年 9 月在爱丁堡举行的第十九届欧洲血液病理学协会(EAHP)会议中关于胃肠道淋巴瘤的两个研讨会的内容。第一个会议侧重于原发性胃肠道 T 细胞和 NK 细胞淋巴增生性疾病的临床和病理特征。强调了前驱病变(RCD 型 2)与肠病相关 T 细胞淋巴瘤之间的区别,包括用于鉴定异常表型的新诊断标志物的讨论。胃肠道惰性 T 细胞淋巴增生性疾病表现出表型异质性,少数病例存在新的分子改变,如 STAT3-JAK2 融合。此外,疾病的新型克隆标志物,如 AXL 和 JAK3 体细胞变异,支持 NK 细胞肠病的肿瘤性质。胃肠道 B 细胞淋巴瘤专题会议主要涉及原发性发生于胃肠道的 B 细胞淋巴瘤增生性疾病(即十二指肠型滤泡淋巴瘤)或优先累及消化道的疾病,如伴有 IRF4 易位的大 B 细胞淋巴瘤和套细胞淋巴瘤(MCL),包括多种分子亚型(即,CCND3 阳性 MCL 模仿 MALT 淋巴瘤)。具有复杂遗传特征的高级别 B 细胞淋巴瘤的疑难病例证明了新型分子诊断方法(如靶向 NGS)的有用性,这些方法可用于识别具有潜在临床影响的高危遗传特征。