病例报告:一名65岁苏丹男子在皇家护理国际医院晚期出现肥厚性心肌病

Elkhansaa Ali Elsheikh Mohamed Elsamani, Duaa Salah Ali Mohamed, Malaz Elnagi Musa Elshiekh
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引用次数: 0

摘要

背景:HCM综合征是在没有其他心脏或其他全身疾病的情况下出现的左心室肥厚。一项流行病学研究报告HCM在普通人群中的患病率为0.02。病例介绍:我们报告一个病例报告65岁的男子谁被转介到诊所后,提出了一个典型的症状。既往病史和家族史不显著。超声心动图显示基底间隔不对称肥厚,射血分数为65%。患者无症状,无功能限制,但后来发生心房颤动并轻度舒张性心力衰竭,经药物治疗和心脏治疗。结论:越早诊断,预后越好。HCM有很多并发症包括心房颤动。因此,了解房颤和其他心律失常与HCM患者相关的频率将降低死亡率,因为可以进行随访心电图和超声心动图检查以预防后续并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Case Report: Late Presentation of Hypertrophic Cardiomyopathy in a 65- Year- Old Sudanese Man at Royal Care International Hospital
Background: HCM Syndrome is a left ventricle hypertrophic in the absence of another cardiac or other systemic condition. An epidemiologic study reported that the prevalence of HCM is 0.02in the general population. Case Presentation: We report a case report of a 65- year- old man who was referred to the clinic after presenting with a typical symptom. Past medical history and family history were insignificant. Echocardiography showed asymmetrical basal septal hypertrophy with a preserved ejection fraction of 65%. The patient was asymptomatic with no functional limitation but later developed atrial fibrillation with mild diastolic heart failure, which was treated by pharmacological medication and cardio version. Conclusion: In conclusion, the earlier the diagnosis, better the prognosis. HCM has a lot of complications including atrial fibrillation. Therefore, awareness of how often AF and other arrhythmias are associated with HCM patients will lead to lower mortality as a follow-up ECG and echocardiography can be performed to prevent subsequent complications.
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