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Fibromuscular Dysplasia Leading to Spontaneous Coronary Artery Dissection with Sudden Cardiac Arrest

机译:纤维肌发育异常导致心脏猝死的自发性冠状动脉夹层

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A 30-year-old previously healthy female, who was six-week postpartum, experienced sudden collapse and tonic-clonic seizure. Emergency medicine services arrived at the scene and the patient was found to be in ventricular fibrillation. Advanced cardiovascular life support (ACLS) was initiated with return of spontaneous circulation. Afterwards, her initial EKG showed atrial fibrillation with rapid ventricular rate, ST elevation in leads II, III, and aVF, and ST depression in V2–V4. She was transferred to a tertiary care hospital where emergent angiogram was performed revealing obstruction of blood flow in the proximal and mid right coronary artery (RCA). A hazy and irregularly contoured appearance of the RCA was consistent with diagnosis of fibromuscular dysplasia. Subsequently, intravascular ultrasonogram (IVUS) was performed which confirmed the diagnosis of RCA dissection. Successful revascularization of the RCA was performed using two bare mental stents. After a complicated course in hospital, she was discharged in stable condition and did very well overall.
机译:一名30岁以前健康的女性,产后六周,经历了突然的虚脱和强直性阵挛性癫痫发作。紧急医疗服务到达现场,发现该患者患有心室纤颤。随着自发循环的恢复,开始了高级心血管生命支持(ACLS)。此后,她最初的心电图表现为房颤伴快速心室率,II,III和aVF导联ST升高,V2-V4导联ST压低。她被转到三级医院,在那里进行了紧急血管造影检查,结果显示冠状动脉近端和右中部血流阻塞。 RCA的轮廓模糊且轮廓不规则与纤维肌发育异常的诊断一致。随后,进行了血管内超声检查(IVUS),证实了RCA夹层的诊断。使用两个裸露的心理支架成功进行了RCA的血运重建。经过复杂的住院治疗,她出院后病情稳定,总体表现很好。

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