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伪装成血栓闭塞性脉管炎的原发性难治性灾难性抗磷脂综合征

Primary Refractory Catastrophic Antiphospholipid Syndrome Masquerading as Buerger's Disease.

作者信息

Tannous Toufic, Rosso Claudia, Iannuccilli Jenna, Tannous Karim, Keating Matthew

机构信息

Internal Medicine, Roger Williams Medical Center/Boston University, Providence, USA.

School of Medicine, University of California - Irvine, Irvine, USA.

出版信息

Cureus. 2021 Apr 7;13(4):e14350. doi: 10.7759/cureus.14350.

Abstract

Catastrophic antiphospholipid syndrome (CAPS) is a lethal disease with up to 30% mortality rate. It can occur as a primary disease or secondary to an underlying autoimmune disease. Current treatment focuses on disease control with anticoagulation and steroids. Plasma exchange and intravenous immunoglobulin (IVIG) have shown some benefit when added. Monoclonal drugs such as rituximab have shown some benefit in refractory cases, and eculizumab, a drug approved for use in atypical hemolytic uremic syndrome, has demonstrated disease control in a few case reports. We describe a unique case of primary refractory CAPS with an unusual presentation that was treated with five lines of therapy before disease control was established.

摘要

灾难性抗磷脂综合征(CAPS)是一种致死性疾病,死亡率高达30%。它可作为原发性疾病出现,也可继发于潜在的自身免疫性疾病。目前的治疗重点是通过抗凝和使用类固醇来控制疾病。血浆置换和静脉注射免疫球蛋白(IVIG)在加用时已显示出一定益处。诸如利妥昔单抗等单克隆药物在难治性病例中已显示出一定益处,而一种被批准用于非典型溶血尿毒综合征的药物依库珠单抗,在一些病例报告中已证明可控制病情。我们描述了一例原发性难治性CAPS的独特病例,其表现不寻常,在病情得到控制之前接受了五种治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f975/8104915/a883245cdcf2/cureus-0013-00000014350-i01.jpg

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