下肢严重缺血迟发性抗磷脂综合征1例临床治疗成功

I. M. Sadreeva, A. A. Sadreeva, A. V. Maksimov
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引用次数: 0

摘要

抗磷脂综合征(APS)的特点是非炎症性血栓性血管病变,病变的血管类型和局部。这就是为什么APS的临床表现多种多样,患者求助于不同的医生。本文报道一例急性下肢缺血的临床病例。患者为62岁女性,门诊观察2年,临床表现为间歇性跛行,诊断为下肢动脉粥样硬化。同时,脾动脉血栓形成史-不典型动脉粥样硬化,实验室现象:假阳性Wassermann反应和延长磷脂依赖试验(APTT)提示APS。患者因下肢严重缺血,有截肢危险而入住共和国临床医院血管外科。检测抗磷脂抗体。由于APS的治疗病因,避免了下肢截肢。目前的临床病例表明,APS可能发生在60岁以上的人群中,所有专业的医生都应该警惕这种诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical case of successful treatment of a patient with critical lower limb ischemia as a late onset of antiphospholipid syndrome
The antiphospholipid syndrome (APS) is characterized by non-inflammatory thrombotic vasculopathy with lesions of vessels of all types and localization. That is why clinical manifestations of APS are varied and patients turn to various physicians. The article describes a clinical case of a critical lower limb ischemia in AP. A 62 y. o. female patient was under outpatient observation for two years with the clinic of intermittent claudication and a diagnosis of atherosclerosis of lower limb arteries. At the same time, a history of thrombosis of the splenic artery — atypical for atherosclerosis, laboratory phenomena: a false-positive Wassermann reaction and an elongation of the phospholipid-dependent test (APTT) indicated APS. The patient was admitted into Department of Vascular Surgery of the Republic Clinical Hospital with critical lower limb ischemia and a threat of amputation. Antiphospholipid antibodies were detected. Due to the therapy pathogenetic for APS, amputation of the lower extremity was avoided. The presented clinical case shows that the APS may occur in people older than 60, and physicians of all specialties should be alert to this diagnosis.
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