Suppr超能文献

[与十二指肠黏膜相关淋巴组织淋巴瘤相关的γ重链病]

[Gamma-heavy chain disease associated with MALT lymphoma of the duodenum].

作者信息

Ieko M, Kohno M, Ohmoto A, Notoya A, Fukazawa Y, Yasukouchi T, Sawada K, Koike T

机构信息

Department of Internal Medicine, School of Dentistry, Health Science University of Hokkaido.

出版信息

Rinsho Ketsueki. 1998 Jul;39(7):512-8.

PMID:9750459
Abstract

We report a case of a 63-year-old woman with gamma heavy chain disease (HCD) associated with mucosa-associated lymphoid tissue (MALT) lymphoma of the duodenum. She was suffering from drug-resistant tonsillitis with high fever. Examination on admission showed leukocytopenia and thrombocytopenia. Bone marrow aspirate revealed granulocytosis and a hypocellular marrow with no increase in plasma cells or atypical lymphocytes. Serum electrophoresis disclosed, in addition to hypogamma-globulinemia, an abnormal band due to the presence of gamma HCD protein. This abnormal protein was a molecular weight of approximately 40 kd as determined by Western blots technique, and belonged to the IgG1 subclass as determined by ELISA with monoclonal antibodies against IgG. An endoscopic examination of the patient's duodenum found a small tumorous lesion, which was confirmed pathologically to be MALT lymphoma. HCD is known to be associated with lymphoproliferative diseases. In this case, gamma HCD had developed as a secondary complication of MALT lymphoma. gamma HCD associated with MALT lymphoma of the duodenum is rare in the literature.

摘要

我们报告一例63岁女性,患有与十二指肠黏膜相关淋巴组织(MALT)淋巴瘤相关的γ重链病(HCD)。她患有耐药性扁桃体炎并伴有高热。入院检查显示白细胞减少和血小板减少。骨髓穿刺显示粒细胞增多,骨髓细胞减少,浆细胞或非典型淋巴细胞无增加。血清电泳显示,除了低γ球蛋白血症外,由于存在γHCD蛋白还出现了一条异常带。通过蛋白质印迹技术测定,这种异常蛋白的分子量约为40kd,通过使用抗IgG单克隆抗体的ELISA测定,其属于IgG1亚类。对患者十二指肠进行内镜检查发现一个小肿瘤性病变,经病理证实为MALT淋巴瘤。已知HCD与淋巴增殖性疾病有关。在本病例中,γHCD是作为MALT淋巴瘤的继发性并发症出现的。十二指肠MALT淋巴瘤相关的γHCD在文献中很少见。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验