Cardiac pathologic findings in 3 unusual cases of sudden cardiac death related to anorexiant drugs

摘要

Summary Amphetamine congeners can be prescribed as anorexiant drugs despite their potential adverse effects, including cardiac toxicity. However, the morphologic features of cardiac damage related to protracted use of these compounds are unknown. We provide a detailed description of cardiac autopsy findings in 3 cases of sudden death associated with protracted use of high doses of phendimetrazine and/or phenylpropanolamine or bupropion prescribed as anorexiants, in association with other compounds. The main cardiac findings were similar in all 3 cases: (1) mild-moderate hypertrophy of the left ventricle and/or the septum; (2) myocardial nonischemic scarring (midmural and/or subepicardial) appearing as discrete foci or with a bandlike morphology; (3) mild-moderate intramural small vessel disease in the absence of significant epicardial coronary artery stenosis; and (4) acute/recent inflammatory lesions consistent with toxic myocarditis. In summary, the detailed pathology examination of the heart in these 3 cases revealed myocardial lesions identical to those reported in catecholamine myocardial damage in all their various stages of evolution. In the presence of a clinical history of long-term intake of anorexiants of this category, it is most important at autopsy to recognize and correctly interpret the acute and chronic myocardial lesions of the type herein described because they represent an anatomical substrate for arrhythmic death. Highlights " Amphetamine congeners can be prescribed as anorexiant drugs despite their potential adverse effects, including cardiac toxicity, which could lead to sudden cardiac death. " Detailed examination of the hearts at autopsy reveals myocardial lesions similar to those reported in catecholamine-related myocardial damage. " In sudden death cases with a clinical history of long-term intake of anorexiants, it is of utmost importance to recognize and correctly interpret these lesions because they represent an anatomical substrate for arrhythmic death.