Schreuder Max I, van den Brand Michiel, Hebeda Konnie M, Groenen Patricia J T A, van Krieken J Han, Scheijen Blanca
Department of Pathology, Radboud University Medical Center, Geert Grooteplein Zuid 10, 6525 AG Nijmegen, The Netherlands.
Pathology-DNA, Rijnstate Hospital, Arnhem, The Netherlands.
J Hematop. 2017 Sep 25;10(3-4):91-107. doi: 10.1007/s12308-017-0302-2. eCollection 2017 Dec.
Extranodal marginal zone lymphoma (EMZL), mostly represented by mucosa-associated lymphoid tissue (MALT) type, also referred to as MALT lymphoma, is a clinically heterogeneous entity within the group of low-grade B cell lymphomas that arises in a wide range of different extranodal sites, including the stomach, lung, ocular adnexa, and skin. It represents the third most common non-Hodgkin lymphoma in the Western world, and the median age of occurrence is around 60 years. One characteristic aspect in a subset of EMZL detectable in about 25% of the cases is the presence of specific chromosomal translocations involving the genes and , which lead to activation of the NF-κB signaling pathway. Another unique aspect is that several infectious agents, such as in the case of gastric EMZL, and autoimmune disorders, like Sjögren syndrome, have been implicated in the pathogenesis of this cancer. Recent findings as summarized in this review have further improved our understanding of the complex pathobiology of this disease and have been essential to better define novel treatment strategies. In addition, many of these specific features are currently being implemented for the diagnosis of EMZL.
结外边缘区淋巴瘤(EMZL),大多由黏膜相关淋巴组织(MALT)型代表,也称为MALT淋巴瘤,是一组低度B细胞淋巴瘤中的临床异质性实体,发生于广泛的不同结外部位,包括胃、肺、眼附属器和皮肤。它是西方世界第三常见的非霍奇金淋巴瘤,发病的中位年龄约为60岁。在约25%的病例中可检测到的EMZL亚组的一个特征是存在涉及某些基因的特定染色体易位,这会导致NF-κB信号通路激活。另一个独特之处在于,几种感染因子,如胃EMZL中的某种感染因子,以及自身免疫性疾病,如干燥综合征,都与这种癌症的发病机制有关。本综述总结的最新发现进一步增进了我们对这种疾病复杂病理生物学的理解,对于更好地确定新的治疗策略至关重要。此外,目前许多这些特定特征正被用于EMZL的诊断。