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肥厚型心肌病是常染色体显性遗传的心肌病,表现为心室的肥厚、心室充盈受限和顺应性的下降。而肺动脉瘤是一种罕见的心血管疾病,表现为肺动脉的异常扩张,可导致严重的心血管事件,包括心力衰竭、咯血、动脉瘤破裂、猝死等。我们确诊1例罕见的肥厚型心肌病合并肺动脉瘤患者,其病程长达20余年,具体病史见下。1病例资料患者,男,84岁,因“活动后胸闷气短20余年,加重2个月”就诊。该患者20年前开始出现活动
Hypertrophic cardiomyopathy is an autosomal dominant cardiomyopathy characterized by ventricular hypertrophy, limited ventricular filling, and decreased compliance. Pulmonary aneurysm, on the other hand, is a rare cardiovascular disease characterized by abnormal expansion of pulmonary arteries that can lead to serious cardiovascular events including heart failure, hemoptysis, aneurysm rupture, and sudden death. We diagnosed a rare hypertrophic cardiomyopathy patients with pulmonary aneurysm, the duration of up to 20 years, the specific history see below. 1 case data patients, male, 84 years old, because of “chest tightness after shortness of breath more than 20 years, increased 2 months ” treatment. The patient started to appear 20 years ago