Cardiac involvement in light chain amyloidosis: a case report
Jing LI
Hong-Yan WANG
Ning BIAN
Ru-Yi XU
Can HUA
Shao-Li NIU
Zhuo-Kun GAN
Qing WANG
Hai-Tao TIAN
1.VIP Cardiovascular Department, the Sixth Medical Center of Chinese PLA General Hospital, Beijing, China2.VIP Cardiovascular Department, the Sixth Medical Center of Chinese PLA General Hospital, Beijing, China3.VIP Cardiovascular Department, the Sixth Medical Center of Chinese PLA General Hospital, Beijing, China4.VIP Cardiovascular Department, the Sixth Medical Center of Chinese PLA General Hospital, Beijing, China5.VIP Cardiovascular Department, the Sixth Medical Center of Chinese PLA General Hospital, Beijing, China6.VIP Cardiovascular Department, the Sixth Medical Center of Chinese PLA General Hospital, Beijing, China7.VIP Cardiovascular Department, the Sixth Medical Center of Chinese PLA General Hospital, Beijing, China8.VIP Cardiovascular Department, the Sixth Medical Center of Chinese PLA General Hospital, Beijing, China9.VIP Cardiovascular Department, the Sixth Medical Center of Chinese PLA General Hospital, Beijing, China
摘要：Amyloidosis refers to a group of heterogeneous diseases in which amyloid fibers deposited in organ and extracellular tissue comprise misfolded precursor proteins.[1] According to the variety of misfolded proteins,the site of production and the type of tissue infiltrated,amyloidosis of the myocardium is divided into five subtypes:immunoglobulin light chain (AL),secondary amyloidosis (or reactive amyloidosis),familial amyloidosis [transthyretin (ATTR) amyloidosis or hereditary amyloidosis],dialysis-related amyloidosis,and senile systemic amyloidosis.
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论文发表日期：2020-06-28
在线出版日期：2025-08-15（本平台首次上网日期，不代表文献的发表时间）
页数：6( 373-378 )
英文信息