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Hypertrophic cardiomyopathy associated with left ventricular aneurysm and normal coronary arteries: Case study indicating genetic tendencies of cardiomyopathy

机译:肥厚型心肌病伴左室动脉瘤和正常冠状动脉:案例研究表明心肌病的遗传倾向

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摘要

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.
机译:一名50岁的男性患者出现肥厚性梗阻性心肌病(HOC),伴有左心室动脉瘤和正常冠状动脉。他的病史显示没有心肌梗塞或非典型心绞痛的证据。体格检查显示HOC,但未提示存在动脉瘤。尽管患者接受了药物治疗,但随后出现心力衰竭,并且在农场工作时突然死亡。随后对该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,在22岁的大男人中尤为明显。讨论了HOC与左心室动脉瘤之间可能的血液动力学关系,以及可能的迹象。左室动脉瘤的作用也与疾病的自然病史有关。

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