关键词: 99mTc-HMDP, 99mTc-hydroxymethylene diphosphonate AL amyloidosis AL, immunoglobulin light-chain amyloidosis ATTR amyloidosis ATTR, transthyretin amyloidosis CA, cardiac amyloidosis CMR, cardiac magnetic resonance HF, heart failure Ig, immunoglobulin LV, left ventricular LVEF, left ventricular ejection fraction NT-proBNP, N-terminal pro–B-type natriuretic peptide cardiac amyloidosis hs-cTnT, high-sensitivity cardiac troponin T

来  源:   DOI:10.1016/j.jaccas.2020.12.047   PDF(Sci-hub)   PDF(Pubmed)

Abstract:
Currently adopted diagnostic flow charts consider transthyretin and light-chain cardiac amyloidosis as mutually exclusive. Here, we report for the first time, to our knowledge, the demonstration of a biopsy-proven dual pathology in an 80-year-old man with sequential development of both wild-type transthyretin amyloidosis and light-chain cardiac amyloidosis cardiomyopathy over a 3-year timespan. (Level of Difficulty: Intermediate.).
摘要:
目前采用的诊断流程图认为运甲状腺素蛋白和轻链心脏淀粉样变性是相互排斥的。这里,我们第一次报道,根据我们的知识,在一名80岁的男性患者中,显示活检证实的双重病理,在3年的时间内连续发展为野生型甲状腺素运载蛋白淀粉样变性和轻链心脏淀粉样变性心肌病.(难度等级:中级。).
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