Jeon Ja Young, Lim Sun Gyo, Kim Jang Hee, Lee Kee Myung, Cho Sung Ran, Han Jae Ho
Department of Internal Medicine, Ajou University Hospital, Ajou University School of Medicine, Suwon, Korea.
Department of Gastroenterology, Ajou University Hospital, Ajou University School of Medicine, Suwon, Korea.
Blood Res. 2013 Dec;48(4):287-91. doi: 10.5045/br.2013.48.4.287. Epub 2013 Dec 24.
Nodular lymphoid hyperplasia of the stomach is a rare lymphoproliferative disorder. Here, we report a 38-year-old man who presented with multiple submucosal tumors of the stomach. Histologically, the lesions were characterized by multiple discrete submucosal nodules of lymphoid cells. The infiltrates between the lymphoid follicles were composed mainly of medium-sized lymphoid cells with abundant clear cytoplasm, as well as a few large cells with vesicular nuclei. The gastric mucosa exhibited multifocal lymphoid aggregates and some of the epithelial cells were infiltrated by small lymphocytes mimicking lymphoepithelial lesions. Histopathology was consistent with mucosa-associated lymphoid tissue lymphoma. However, the infiltrating lymphoid cells were positive for CD2, CD3, CD5, and CD7. In addition, polymerase chain reaction analysis of the immunoglobulin heavy chain and T-cell receptor gene rearrangements demonstrated polyclonality. This case was diagnosed as reactive lymphoid hyperplasia of the stomach.
胃结节性淋巴组织增生是一种罕见的淋巴增殖性疾病。在此,我们报告一名38岁男性,其表现为胃多发黏膜下肿瘤。组织学上,病变的特征为多个离散的黏膜下淋巴样细胞结节。淋巴滤泡之间的浸润主要由具有丰富透明细胞质的中等大小淋巴样细胞以及一些具有泡状核的大细胞组成。胃黏膜呈现多灶性淋巴样聚集,部分上皮细胞被小淋巴细胞浸润,类似淋巴上皮病变。组织病理学与黏膜相关淋巴组织淋巴瘤一致。然而,浸润的淋巴样细胞CD2、CD3、CD5和CD7呈阳性。此外,免疫球蛋白重链和T细胞受体基因重排的聚合酶链反应分析显示为多克隆性。该病例被诊断为胃反应性淋巴组织增生。