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双克隆丙种球蛋白病——1例原发性胃肠道淋巴瘤病例报告

Biclonal gammopathy--report of a case with primary gastrointestinal lymphoma.

作者信息

Wang C R, Lai H S, Lee G L, Chuang C Y

机构信息

Department of Internal Medicine, National Taiwan University Hospital, Taipei, R.O.C.

出版信息

Zhonghua Min Guo Wei Sheng Wu Ji Mian Yi Xue Za Zhi. 1991 Nov;24(4):359-64.

PMID:1845345
Abstract

A 61-year-old female patient had had abdominal pain for two months; primary gastrointestinal lymphoma of diffuse, large cell type histology was diagnosed. Bone marrow study was negative. Bimodal gamma globulin was found on serum protein electrophoresis. Immunoelectrophoresis and immunofixation confirmed the nature of biclonal gammopathy with a fast-migrating IgM-kappa band and a slow-migrating IgG-kappa band. Biclonal gammopathy is unusual, and only rarely have cases been reported. The immunologic and molecular implications of biclonal gammopathy are discussed.

摘要

一名61岁女性患者腹痛两个月;诊断为弥漫大细胞型组织学的原发性胃肠道淋巴瘤。骨髓检查为阴性。血清蛋白电泳发现双峰γ球蛋白。免疫电泳和免疫固定证实了双克隆丙种球蛋白病的性质,有一条快速迁移的IgM-κ带和一条缓慢迁移的IgG-κ带。双克隆丙种球蛋白病不常见,仅有极少病例报道。本文讨论了双克隆丙种球蛋白病的免疫学和分子学意义。

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