AL amyloidosis: advances in diagnosis and management

被引:11
|
作者
Koh, Youngil [1 ]
机构
[1] Seoul Natl Univ Hosp, Dept Internal Med, 101 Daehak Ro, Seoul 03080, South Korea
关键词
AL amyloidosis; SAP; Pathophysiology; Treatment; LIGHT-CHAIN AMYLOIDOSIS; STAGING SYSTEM;
D O I
10.5045/br.2020.S009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Light chain (AL) amyloidosis is a disease in which malignant plasma cell clones affect multiple organs including the heart and kidney. The mechanism for organ function deterioration in AL amyloidosis differs from multiple myeloma. Thus, not all agents used to treat multiple myeloma shows similar efficacy in AL amyloidosis. In AL amyloidosis, both hematologic and organ responses after treatment are important to improve the clinical outcome. Especially, improving heart function is one of the key aspects in the treatment of AL amyloidosis. With recent advances in the understanding of the pathophysiologic mechanism of AL amyloidosis, novel treatment methods are under active trial. In this article, I have reviewed the advances in pathophysiology, diagnosis, risk stratification, and treatment of AL amyloidosis.
引用
收藏
页码:54 / 57
页数:4
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