Al Hazzouri Antonio, Daou Rose-Mary, Attieh Philippe, Ibrahim Zahi, Ghadieh Hilda E, Harbieh Bernard
Department of Biomedical Sciences, Faculty of Medicine and Medical Sciences, University of Balamand, Koura, Lebanon.
Am J Case Rep. 2025 Jul 4;26:e948092. doi: 10.12659/AJCR.948092.
BACKGROUND Cardiac amyloidosis is the accumulation of aberrant proteins in the heart, liver, brain, and several other organs. It presents both extracardiac and cardiac symptoms, making diagnosis difficult and early detection crucial in the prognosis of the patient. Diagnostic techniques for cardiac amyloidosis can present false-negative results, making diagnosis difficult in the early stage of the disease. CASE REPORT A 67-year-old man presented for worsening dyspnea of several months' duration and recent cough. Echocardiography study showed unexplained biventricular hypertrophy with preserved left ventricular systolic function, and a restrictive filling pattern suggesting an infiltrative heart disease like cardiac amyloidosis. Technetium pyrophosphate scan, light-chain assay, and serum and urine protein immunofixation were negative. The patient was treated as a case of advanced heart failure, with initial improvement. He started deteriorating progressively, and repeating the workup was considered. Six months later, a repeated echocardiogram showed severely impaired left ventricular systolic function and findings suggestive of advanced cardiac amyloidosis. Free light-chain assay was positive, in favor for AL amyloidosis, which was confirmed by a bone marrow biopsy and cardiac MRI. Chemotherapy was started, but the patient died due to stage D heart failure caused by advanced AL amyloidosis. CONCLUSIONS We aim at increasing awareness of the early diagnosis of cardiac amyloidosis and highlighting the importance of considering the disease even with an initial negative workup. We will also try to explain the reason for the false-negative initial workup and to implement the use of cardiac MRI in early stages if the clinical suspicion for the disease is high.
心脏淀粉样变性是异常蛋白质在心脏、肝脏、大脑和其他几个器官中的积聚。它会出现心外和心脏症状,这使得诊断困难,而早期检测对患者的预后至关重要。心脏淀粉样变性的诊断技术可能会出现假阴性结果,导致在疾病早期难以诊断。
一名67岁男性因持续数月的呼吸困难加重和近期咳嗽前来就诊。超声心动图检查显示原因不明的双心室肥厚,左心室收缩功能保留,以及提示浸润性心脏病如心脏淀粉样变性的限制性充盈模式。焦磷酸锝扫描、轻链检测以及血清和尿蛋白免疫固定电泳均为阴性。该患者被当作晚期心力衰竭病例进行治疗,最初有改善。但他随后病情逐渐恶化,于是考虑再次进行检查。六个月后,重复超声心动图显示左心室收缩功能严重受损,提示晚期心脏淀粉样变性。游离轻链检测呈阳性,支持AL型淀粉样变性,骨髓活检和心脏磁共振成像证实了这一点。开始进行化疗,但患者因晚期AL型淀粉样变性导致的D期心力衰竭死亡。
我们旨在提高对心脏淀粉样变性早期诊断的认识,并强调即使初始检查结果为阴性也需考虑该病的重要性。我们还将尝试解释初始检查结果为假阴性的原因,并在临床高度怀疑该病的早期阶段采用心脏磁共振成像。