Cid Puente Ricardo, Melchor Bonilla Erick R, Huerta Alvarado Alma P, Aguirre Moreno Paola D
Department of Immunology, School of Biological Sciences, Universidad Autónoma de Zacatecas, Zacatecas, MEX.
Department of Internal Medicine, Centenario Hospital Miguel Hidalgo, Aguascalientes, MEX.
Cureus. 2025 Apr 2;17(4):e81621. doi: 10.7759/cureus.81621. eCollection 2025 Apr.
Catastrophic antiphospholipid syndrome (CAPS) is the most aggressive and severe form of antiphospholipid syndrome (APS). Due to its rarity and highly variable clinical presentation, diagnosing CAPS is extremely challenging, often leading to delayed treatment initiation and a high rate of mortality and morbidity. In this paper, we report the case of a 39-year-old male patient with no prior diagnosis of APS who initially presented with deep vein thrombosis in the left leg. The condition rapidly progressed to multiple thromboses in the lungs, liver, spleen, and left kidney. The diagnosis of CAPS was confirmed by the presence of lupus anticoagulant, and treatment was initiated 48 hours after symptom onset with high doses of steroids and anticoagulants. However, the patient developed multiple organ failure and died 72 hours after admission. This paper aims to highlight the rapid progression of CAPS, its fatal complications, and the critical importance of initiating treatment as quickly as possible, even before confirmation through laboratory or histopathological studies.
灾难性抗磷脂综合征(CAPS)是抗磷脂综合征(APS)最严重且侵袭性最强的形式。由于其罕见性以及临床表现高度多变,诊断CAPS极具挑战性,常常导致治疗开始延迟以及高死亡率和高发病率。在本文中,我们报告了一例39岁男性患者,此前未诊断出APS,最初表现为左腿深静脉血栓形成。病情迅速发展为肺部、肝脏、脾脏和左肾的多处血栓形成。狼疮抗凝物的存在确诊了CAPS,症状出现后48小时开始使用大剂量类固醇和抗凝剂进行治疗。然而,患者出现多器官功能衰竭,入院72小时后死亡。本文旨在强调CAPS的快速进展、其致命并发症以及尽早开始治疗的至关重要性,即使在通过实验室或组织病理学研究确诊之前。