Gastric MALT lymphoma presenting as Waldenstrom's macroglobulinemia without bone marrow involvement

被引:3
|
作者
Salle, Valery
Smail, Amar
Joly, Jean-Paul
Capiod, Jean-Claude
Gontier, Marie-Francine
Duhaut, Pierre
Ducroix, Jean-Pierre
机构
[1] Amiens Univ Hosp, Dept Internal Med, F-80054 Amiens, France
[2] Amiens Univ Hosp, Dept Gastroenterol & Hepatol, Amiens, France
[3] Amiens Univ Hosp, Hematol Lab, Amiens, France
[4] Amiens Univ Hosp, Dept Pathol, Amiens, France
来源
CLINICAL LYMPHOMA & MYELOMA | 2007年 / 7卷 / 07期
关键词
hyperviscosity; immunoglobulin; lymphoplasmacytic lymphoma;
D O I
10.3816/CLM.2007.n.029
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We report a case of gastric mucosa-associated lymphoid tissue (MALT) lymphoma with macroglobulinemia in a 59-year-old man who presented with melena. A computed tomography scan of the abdomen showed irregular thickening of the wall of the stomach, and endoscopic examination disclosed enlarged and inflammatory folds of the fundus. Histopathologic examination of gastric samples showed mucosal infiltration by small lymphocytes, which were positive for CD20 and negative for CD10 and CD23, confirming the diagnosis of gastric MALT lymphoma. Serum electrophoresis detected a monoclonal peak and immunoelectrophoresis revealed an immunoglobulin M K component. Bone marrow aspirate and biopsy results were normal. The patient received chemotherapy. After treatment, he was in complete remission, and the serum monoclonal component had disappeared. Our observation is uncommon because of important macroglobulinemia occurring in gastric MALT lymphoma without bone marrow involvement.
引用
收藏
页码:470 / 471
页数:2
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