在一位老年患者中诊断出ALCAPA
Thomas C Pointer1, John F Keaney1, Samuel W Reinhardt2
1Department of Pediatrics, Yale School of Medicine, New Haven, Connecticut, USA; Yale-New Haven Hospital, New Haven, Connecticut, USA.
从肺动脉产生异常的左冠状动脉起源 (ALCAPA) 是罕见的,通常在婴儿期致命. 这个案例显示了一名66岁的女性,患有未诊断的ALCAPA,仅仅通过医疗管理,她仍然无症状.
科学领域:
- 心脏病学 心脏病学
- 遗传性心脏病是一种先天性心脏病.
背景情况:
- 从肺动脉引起的异常左冠状动脉起源 (ALCAPA) 是一种罕见的先天性心脏缺陷,影响不到人口的0.01%.
- 症状通常在生命的前3个月内表现出来,在没有手术修复的情况下死亡率很高.
研究的目的:
- 报告一个罕见的成人发病ALCAPA病例.
- 讨论对成年ALCAPA患者保守治疗的影响.
主要方法:
- 一个66岁的妇女的案例介绍,她以前没有被诊断出ALCAPA.
- 审查患者的医疗管理,附带循环和右冠状动脉扩张.
主要成果:
- 患者在没有手术干预的情况下,在成年期保持无症状.
- 显著的抵押和扩张的右冠状动脉有助于患者的良好结果.
结论:
- 在罕见的情况下,ALCAPA可以与没有手术的成年生存相兼容.
- 成年人呈现ALCAPA需要仔细考虑基于症状,药物治疗和手术风险的手术与保守治疗.
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