首页> 美国卫生研究院文献>Case Reports in Rheumatology >Spontaneous Coronary Artery Dissection in a Male Patient with Takayasus Arteritis and Antiphospholipid Antibody Syndrome
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Spontaneous Coronary Artery Dissection in a Male Patient with Takayasus Arteritis and Antiphospholipid Antibody Syndrome

机译:Takayasu动脉炎和抗磷脂抗体综合征的男性患者的自发性冠状动脉夹层

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摘要

We present a case of a 34-year-old male who presented to the emergency ward with fever and abdominal pain. The diagnosis of Takayasu's arteritis and also antiphospholipid syndrome was made during an imaging workup of deep-vein thrombosis. A spontaneous coronary artery dissection was revealed in coronary CT angiography requested for chest pain and dyspnea. The patient was treated medically and discharged on close followup. The concurrence of spontaneous coronary artery dissection with antiphospholipid syndrome and Takayasu's arteritis has not been reported in the previous literature. The possibility of a spontaneous coronary artery dissection should be considered in patients presenting with both diseases.
机译:我们介绍了一例34岁的男性,他因发烧和腹痛而到急诊病房就诊。在深静脉血栓形成的影像学检查过程中,诊断出了Takayasu的动脉炎以及抗磷脂综合征。要求进行胸痛和呼吸困难的冠状动脉CT血管造影显示有自发性冠状动脉夹层。该患者已接受药物治疗,并在密切随访中出院。在以前的文献中,尚无自发性冠状动脉夹层合并抗磷脂综合征和高津动脉炎的报道。患有两种疾病的患者均应考虑自发性冠状动脉解剖的可能性。

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