A patient with hereditary spherocytosis and silicosis who developed an IgA(.LAMBDA.) monoclonal gammopathy.
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A patient with hereditary spherocytosis and silicosis who developed an IgA (λ.) monoclonal gammopathy is reported. It was thought that a combination of hereditary factors, a chronic hemolytic stimulus to the reticuloendothelial system and an adjuvant effect provided by presence of diffuse silica might have contributed to the development of monoclonal gammopathy.
- 社団法人 日本内科学会の論文
社団法人 日本内科学会 | 論文
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