Concurrent Therapy for Immunoglobulin Light Chain Cardiac Amyloidosis and Transthyretin Cardiac Amyloidosis: A Case Report

被引:0
|
作者
Horigome, Yuichi [1 ]
Ishii, Shunsuke [2 ]
Matsumoto, Manabu [3 ]
Ikeda, Yoshihiko [3 ]
Hatakeyama, Kinta [3 ]
Ako, Junya [2 ]
Suzuki, Takahiro [1 ]
机构
[1] Kitasato Univ, Sch Med, Dept Hematol, Tokyo, Japan
[2] Kitasato Univ, Sch Med, Dept Cardiovasc Med, Tokyo, Japan
[3] Natl Cerebral & Cardiovasc Ctr, Dept Pathol, Osaka, Japan
关键词
AL-amyloidosis; ATTR-amyloidosis; daratumumab; tafamidis; safety; MONOCLONAL GAMMOPATHY; AL AMYLOIDOSIS; STRATIFICATION; PREVALENCE; DIAGNOSIS;
D O I
10.2169/internalmedicine.4526-24
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cardiac amyloidosis (CA), predominantly caused by amyloid transthyretin (ATTR) or immunoglobulin light chain (AL), has a poor prognosis, and a precise diagnosis is crucial because the optimal treatments differ between the two conditions. However, diagnosing AL-CA is challenging because of the unavailability of effective AL-detecting antibodies, particularly in cases with coexisting AL- and ATTR-CA. This report presents a successfully diagnosed case of complicated AL- and ATTR-CA that was successfully treated with tafamidis for ATTR-CA and combination chemotherapy for AL-CA. This case highlights the importance of a precise diagnosis of CA and supports the efficacy and safety of concurrent treatment for coexisting amyloidosis.
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页数:6
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