Edgardo Alania Torres, Susana Olivera Gonzalez, Sergio Luengo Perez, Paula Bertomeu Perez, Beatriz Molines Charbonnier
Department of Cardiology, Denia Hospital, Alicante, Spain.
Department of Internal Medicine, Denia Hospital, Alicante, Spain.
JACC Case Rep. 2025 Sep 3;30(26):104924. doi: 10.1016/j.jaccas.2025.104924.
Propionic acidemia (PA) is a rare autosomal recessive metabolic disorder, typically presenting in infancy. Cardiac involvement in adults is uncommon and underrecognized.
A previously healthy 20-year-old man suffered an out-of-hospital cardiac arrest caused by ventricular fibrillation. Initial evaluation revealed dilated cardiomyopathy, elevated lactate and ammonia levels, and increased propionyl-L-carnitine. Genetic testing identified biallelic pathogenic variants in the PCCB gene, confirming PA. He was managed with a subcutaneous implantable cardioverter-defibrillator, carnitine supplementation, and dietary protein restriction, showing favorable recovery.
This case illustrates a rare late-onset presentation of PA with isolated cardiac symptoms. Such cases highlight the need to consider metabolic cardiomyopathy in young patients with unexplained ventricular arrhythmias and systemic metabolic disturbances.
丙酸血症(PA)是一种罕见的常染色体隐性代谢紊乱疾病,通常在婴儿期发病。成人心脏受累情况并不常见且未得到充分认识。
一名既往健康的20岁男性因室颤发生院外心脏骤停。初始评估显示扩张型心肌病、乳酸和氨水平升高以及丙酰肉碱增加。基因检测确定PCCB基因存在双等位基因致病性变异,确诊为PA。他接受了皮下植入式心律转复除颤器治疗、补充肉碱以及饮食蛋白质限制,恢复情况良好。
本病例说明了PA罕见的迟发性表现,仅有心脏症状。此类病例凸显了对于不明原因室性心律失常和全身代谢紊乱的年轻患者,需要考虑代谢性心肌病。