肥厚性心肌病合并左心室动脉瘤和正常冠状动脉:表明心肌病遗传倾向的病例研究。

Cardiovascular diseases Pub Date : 1981-03-01
C Saenz De La Calzada, A Llovet Verdugo, J Tascon Perez, C Castro Alcaine, A Sanchez Fernandez
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引用次数: 0

摘要

一个50岁的男性提出肥厚性梗阻性心肌病(HOC)与左心室动脉瘤和正常冠状动脉。病史显示无心肌梗塞或非典型心绞痛。体格检查显示为HOC,但未提示动脉瘤的存在。尽管病人接受了医学治疗,但随后心脏衰竭,他在农场工作时突然死亡。随后对患者家属的调查显示,他的五个孩子中有三个也患有心肌病,其中最年长的22岁男子尤为明显。讨论了HOC与左心室动脉瘤之间可能的血流动力学关系,以及可能的适应症。左心室动脉瘤的作用也提出了有关疾病的自然历史。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hypertrophic cardiomyopathy associated with left ventricular aneurysm and normal coronary arteries: Case study indicating genetic tendencies of cardiomyopathy.

A 50-year-old man presented with hypertrophic obstructive cardiomyopathy (HOC) associated with a left ventricular aneurysm and normal coronary arteries. His history revealed no evidence of myocardial infarction or atypical angina. Physical examination disclosed HOC but did not suggest the presence of an aneurysm. Although the patient was treated medically, heart failure ensued, and he died suddenly while working his farm. Subsequent investigation of the patient's family revealed that three of his five children were also affected by cardiomyopathy, which was especially pronounced in the eldest, a 22-year-old man. The possible hemodynamic relationship between HOC and left ventricular aneurysm is discussed, along with probable indications. The role of left ventricular aneurysm is also presented in relation to the natural history of the disease.

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