Skin involvement in the catastrophic antiphospholipid syndrome: A review from CAPS registry.

IF 1.8 4区 医学 Q3 RHEUMATOLOGY
Lupus Pub Date : 2026-08-01 Epub Date: 2026-06-15 DOI:10.1177/09612033261461987
A Ponce, I Rodríguez-Pintó, I Pons, A Jerez, P Toledano, T Rossiñol, B Vilaplana, G Espinosa, R Cervera
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Abstract

ObjectiveTo describe the prevalence, clinical manifestations, histopathological features, and antibody profile associated to skin involvement in patients with catastrophic antiphospholipid syndrome (CAPS).MethodsWe performed a cross-sectional study of the patients included in the "CAPS Registry," a registry developed by the European Forum on Antiphospholipid Antibodies (aPL)1,2 This database contains data from patients with CAPS collected from April 1992 to December 2024. Demographic clinical manifestations, laboratory features (including aPL antibodies), pathological findings in involved skin, and outcome were retrieved.ResultsCutaneous involvement was described in 377 episodes (47%) from 361 patients. A female sex prevalence of 49.4% was observed. The average age was 39.4 (SD ± 17.9) years. The more frequent skin manifestations observed were livedo reticularis (17.6%), skin necrosis (13%), ischemic ulcers (10.4%), skin ischemic (9.7%), skin purpura (7.1%), gangrene (5%), splinter haemorrhages (2.6%), and Raynaud's phenomenon (1.5%). The most frequently affected organs in CAPS episodes with skin involvement were kidneys (72%), lungs (61%), central nervous system (54.5%), and heart (54.4%). Thrombocytopenia and hemolysis features were more common in patients with skin involvement (p < 0.05 for all). Thrombotic microangiopathy was the predominant pathological finding, present in 82 (68.3%) episodes. No difference regarding mortality were found in episodes with or without skin involvement (29.3% vs 32.1%, p = 0.42).ConclusionThe presence of skin involvement in patients with CAPS is frequent. The most frequent manifestations were livedo reticularis and skin necrosis. Skin involvement does not seem to be associated to mortality.

灾难性抗磷脂综合征的皮肤受累:来自CAPS注册的综述。
目的探讨灾难性抗磷脂综合征(CAPS)患者的患病率、临床表现、组织病理学特征以及与皮肤受累相关的抗体谱。方法:我们对欧洲抗磷脂抗体论坛(European Forum on anti - phosplipid Antibodies, aPL)开发的“CAPS Registry”中的患者进行了横断面研究1,2,该数据库包含1992年4月至2024年12月收集的CAPS患者的数据。检索人口学临床表现、实验室特征(包括aPL抗体)、受累皮肤病理结果和结果。结果361例患者中有377例(47%)发生皮肤受累。女性患病率为49.4%。平均年龄39.4 (SD±17.9)岁。常见的皮肤表现为网状活斑(17.6%)、皮肤坏死(13%)、缺血性溃疡(10.4%)、皮肤缺血(9.7%)、皮肤紫癜(7.1%)、坏疽(5%)、碎片性出血(2.6%)和雷诺现象(1.5%)。伴有皮肤受累的CAPS发作中最常受影响的器官是肾脏(72%)、肺(61%)、中枢神经系统(54.5%)和心脏(54.4%)。血小板减少和溶血特征在皮肤受累患者中更为常见(p < 0.05)。血栓性微血管病变是主要的病理表现,出现82次(68.3%)发作。在有或没有皮肤受累的发作中,死亡率没有差异(29.3% vs 32.1%, p = 0.42)。结论CAPS患者皮肤受累发生率高。最常见的表现是网状增生和皮肤坏死。皮肤受累似乎与死亡率无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Lupus
Lupus 医学-风湿病学
CiteScore
4.20
自引率
11.50%
发文量
225
审稿时长
1 months
期刊介绍: The only fully peer reviewed international journal devoted exclusively to lupus (and related disease) research. Lupus includes the most promising new clinical and laboratory-based studies from leading specialists in all lupus-related disciplines. Invaluable reading, with extended coverage, lupus-related disciplines include: Rheumatology, Dermatology, Immunology, Obstetrics, Psychiatry and Cardiovascular Research…
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