Department of Pathology, Duke University Medical Center, Durham, North Carolina 27710, USA.
Arch Pathol Lab Med. 2011 Mar;135(3):394-8. doi: 10.5858/2009-0463-RSR.1.
Primary mediastinal (thymic) large B-cell lymphoma (PMBCL) is a subtype of diffuse large B-cell lymphoma (DLBCL). It commonly presents as a bulky lesion in the anterior-superior mediastinum with symptoms related to local invasion or compression. Microscopic examination typically shows infiltration of medium-large cells surrounded by collagen fibrosis. The neoplastic cells express B-cell markers, and CD30 often shows heterogeneous staining. Comparative genomic hybridization has identified gains in loci of 9p24 and 2p15 as well as Xp11.4-21 and Xq24-26. Amplification of REL and BCL11A at 2p as well as elevated expression of JAK2, PDL1, and PDL2 at 9p has been demonstrated. Nodular sclerosis classic Hodgkin lymphoma needs to be differentiated from PMBCL and cases with overlapped features have been described as mediastinal gray zone lymphoma. Primary mediastinal (thymic) large B-cell lymphoma carries a favorable prognosis in comparison to conventional DLBCL.
原发性纵隔(胸腺)大 B 细胞淋巴瘤(PMBCL)是弥漫性大 B 细胞淋巴瘤(DLBCL)的一种亚型。它通常表现为前上纵隔的巨大肿块,伴有与局部浸润或压迫相关的症状。显微镜下检查通常显示中等大小的细胞浸润,周围有胶原纤维化。肿瘤细胞表达 B 细胞标志物,CD30 常表现为异质性染色。比较基因组杂交已鉴定出 9p24 和 2p15 以及 Xp11.4-21 和 Xq24-26 位点的增益。已经证明了 2p 上 REL 和 BCL11A 的扩增以及 9p 上 JAK2、PDL1 和 PDL2 的高表达。结节性硬化型经典霍奇金淋巴瘤需要与 PMBCL 相鉴别,并且已经描述了具有重叠特征的病例为纵隔灰色区淋巴瘤。与传统的 DLBCL 相比,原发性纵隔(胸腺)大 B 细胞淋巴瘤预后较好。