Navigating Diagnostic Ambiguities in Cardiac Amyloidosis: Insights from a Case with Delayed Diagnosis of AL Amyloidosis

Abstract

Objective: Background: Case Report: Conclusions: Unusual clinical course 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. 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 re-strictive filling pattern suggesting an infiltrative heart disease like cardiac amyloidosis. Technetium pyrophos-phate 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 im-paired 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. 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.