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AL Amyloidosis Mitsuharu Ueda 1 1Department of Neurology, Graduate School of Medical Sciences, Kumamoto University Keyword: アミロイドーシス , フリーライトチェイン , 心アミロイドーシス , 自家末梢血幹細胞移植 , ダラツムマブ , amyloidosis , free light chain , cardiac amyloidosis , autologous stem cell transplantation , daratumumab pp.583-587
Published Date 2024/5/1
DOI https://doi.org/10.11477/mf.1416202647
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Abstract

AL amyloidosis, derived from amyloidogenic immunoglobulin light chains, is a common type of systemic amyloidosis. Peripheral neuropathy has been identified in 10%-40% of patients with systemic AL amyloidosis. Definitive diagnosis requires tissue biopsies, including skin, fat, and gastrointestinal samples, as well as amyloid typing. Disease-modifying therapies have been shown to improve patient survival and prevent progressive organ dysfunction.


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電子版ISSN 1344-8129 印刷版ISSN 1881-6096 医学書院

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