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灾难性抗磷脂综合征:病例报告及文献复习。

Catastrophic antiphospholipid syndrome: a case report and literature review.

机构信息

University of Toledo, College of Medicine and Life Sciences, Toledo, Ohio, USA.

Jobst Vascular Institute, ProMedica Health Network, Hematology Oncology, Toledo, Ohio, USA.

出版信息

J Wound Care. 2024 Sep 1;33(Sup9):S23-S26. doi: 10.12968/jowc.2024.0285.

Abstract

Catatrophic antiphospholipid syndrome (CAPS), a rare variant of antiphospholipid syndrome (APS), is associated with rapid multiorgan failure. While APS is associated with single medium-to-large blood vessel occlusions, CAPS is most often associated with several, concurrent vascular occlusions of small vessels, commonly of the kidneys, heart, skin and brain. We present a case of a 21-year-old female patient with a history of immune thrombocytopenia purpura and APS, who eventually developed concurrent cerebral venous sinus thrombosis, diffuse alveolar haemorrhage, renal thrombotic microangiopathy, and a necrotic, vasculitic wound on her forearm. Despite hospitalisation and treatment, her condition worsened and the patient eventually died after succumbing to suspected CAPS.

摘要

灾难性抗磷脂综合征 (CAPS) 是抗磷脂综合征 (APS) 的一种罕见变体,与多器官迅速衰竭有关。虽然 APS 与单个中等至大血管阻塞有关,但 CAPS 通常与多个同时发生的小血管阻塞有关,常见于肾脏、心脏、皮肤和大脑。我们报告了一例 21 岁女性患者,该患者有免疫性血小板减少性紫癜和 APS 病史,最终并发脑静脉窦血栓形成、弥漫性肺泡出血、肾血栓性微血管病和前臂坏死性血管炎性伤口。尽管住院治疗,但患者病情恶化,最终死于疑似 CAPS。

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