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一名法洛四联症修补术后47岁女性的应激性心肌病

Takotsubo Syndrome in a 47-Year-Old Woman With Repaired Tetralogy of Fallot.

作者信息

Kayani Jehanzeb, Bailey Lelan, Hopkins Kali, Zaidi Ali N, Love Barry

机构信息

Icahn School of Medicine Mount Sinai, New York, New York, USA.

Mount Sinai Adult Congenital Heart Disease Center, Mount Sinai Fuster Heart Hospital, New York, New York, USA.

出版信息

JACC Case Rep. 2025 Jan 15;30(2):102804. doi: 10.1016/j.jaccas.2024.102804.

Abstract

Takotsubo syndrome or broken-heart syndrome is a rare form of nonischemic cardiomyopathy characterized by regional systolic dysfunction of the left ventricle without evidence of coronary artery disease or acute plaque rupture. This transient impairment in myocardial contractility leads to symptoms and signs that can mimic a myocardial infarction. We present a case of Takotsubo syndrome in a 47-year-old premenopausal woman with complex congenital heart disease who initially presented with acute onset of shortness of breath and chest tightness after a verbal altercation. Extremely rare cases of Takotsubo syndrome have been described in the congenital heart disease population in premenopausal women. This case emphasizes the need to highlight acquired cardiac disease in patients with adult congenital heart disease as this cohort continues to age.

摘要

应激性心肌病或心碎综合征是一种罕见的非缺血性心肌病,其特征是左心室局部收缩功能障碍,而无冠状动脉疾病或急性斑块破裂的证据。这种心肌收缩力的短暂损害会导致一些症状和体征,可能类似于心肌梗死。我们报告一例47岁绝经前患有复杂先天性心脏病的女性应激性心肌病病例,该患者最初在一次口角后出现急性气短和胸闷。绝经前患有先天性心脏病的人群中应激性心肌病的病例极为罕见。该病例强调了随着这一群体年龄的增长,有必要关注成年先天性心脏病患者中获得性心脏病的问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc3a/11775812/f0c98782d952/ga1.jpg

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