Missed Cardiac Amyloidosis: A Potentially Treatable Disease

B. Vivek, Ashish Kumar Jain, J. Sawhney, R. Jain, R. Passey, A. Mohanty
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引用次数: 1

Abstract

Aim To highlight the prevailing lack of suspicion of cardiac amyloidosis (CA) amongst physicians, leading to preventable delay in management of patients of heart failure (HF). Methods Six patients of CA diagnosed in 6 months were retrospectively analyzed. Clinical history, investigations, treatment, and follow-up data is analyzed. Result A speckled interventricular septum on echo favored CA. Speckle tracking showed reduced global longitudinal strain with typical left ventricular apical sparing in all patients. Bone marrow study confirmed light chain amyloidosis (AL) in all patients. Conclusion CA, a frequently missed diagnosis, can be detected early with the help of clinical red flag signs, echocardiogram, serum and urine immune electrophoresis and bone scan.
漏诊的心脏淀粉样变性:一种潜在可治疗的疾病
目的强调医生普遍缺乏对心脏淀粉样变性(CA)的怀疑,导致心力衰竭(HF)患者管理的可预防延误。方法对6例6个月确诊的CA患者进行回顾性分析。分析临床病史、调查、治疗和随访资料。结果超声显示室间隔斑点有利于CA。斑点追踪显示所有患者的整体纵向应变减少,并伴有典型的左心室心尖保留。骨髓研究证实所有患者均为轻链淀粉样变性(AL)。结论CA易漏诊,可通过临床红旗征象、超声心动图、血清、尿免疫电泳及骨扫描早期发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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