Multi-organ Involvement in Catastrophic Antiphospholipid Syndrome: A Challenging Case with a Fatal Outcome.

IF 1.3 Q4 RHEUMATOLOGY
Selma Özlem Çelikdelen, Reyhan Bilici
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Abstract

Catastrophic antiphospholipid syndrome (CAPS) is a rare, life-threatening variant of antiphospholipid syndrome (APS) characterized by extensive thrombosis, multi-organ involvement, and high mortality. Despite advances in the understanding and management of APS, CAPS remains a challenge because of its rapidly progressive and potentially lethal course. We report the case of a 33-year-old man with a history of chronic venous insufficiency and recent surgery for chronic thromboembolic pulmonary hypertension (CTEPH) who presented with abdominal pain, exertional dyspnoea, and rapidly worsening clinical status leading to multi-organ dysfunction. Despite aggressive treatment, including anticoagulation, corticosteroids, intravenous immunoglobulin, and immunosuppression, the patient succumbed, highlighting the aggressive nature of CAPS. Initial treatment consisted of anticoagulation with low-molecular-weight heparin and warfarin, supplemented by immunosuppressive therapy including hydroxychloroquine, corticosteroids, and cyclophosphamide. The complexity of management escalated with the development of diffuse alveolar hemorrhage, which required broadspectrum antibiotics and hemodiafiltration for acute renal failure. Despite multidisciplinary efforts and adherence to recommended CAPS protocols, the patient's condition progressively deteriorated, culminating in fatal multiorgan failure. The unpredictable and aggressive nature of CAPS and the limitations of current management strategies are highlighted in this case. This case highlights the need for increased awareness and early aggressive treatment of CAPS patients. It also highlights the importance of ongoing research into more effective treatment modalities and the potential benefits of a multidisciplinary approach in the management of such complex cases. Early recognition and intervention remain critical to the improvement of the prognosis and outcome of patients with CAPS.

重症抗磷脂综合征(CAPS)是抗磷脂综合征(APS)的一种罕见、危及生命的变异型,其特点是广泛的血栓形成、多器官受累和高死亡率。尽管对 APS 的认识和治疗取得了进展,但 CAPS 仍是一项挑战,因为它的病程进展迅速,并可能致命。我们报告了一例 33 岁男性患者的病例,该患者有慢性静脉功能不全病史,近期因慢性血栓栓塞性肺动脉高压(CTEPH)接受过手术治疗,出现腹痛、劳力性呼吸困难,临床状况迅速恶化,导致多器官功能障碍。尽管患者接受了包括抗凝、皮质类固醇、静脉注射免疫球蛋白和免疫抑制在内的积极治疗,但仍不治身亡,突显了 CAPS 的侵袭性。最初的治疗包括使用低分子量肝素和华法林进行抗凝,辅以包括羟氯喹、皮质类固醇和环磷酰胺在内的免疫抑制治疗。随着弥漫性肺泡出血的出现,治疗的复杂性也随之上升,需要使用广谱抗生素和血液透析治疗急性肾衰竭。尽管经过多学科的努力并遵守了推荐的 CAPS 方案,但患者的病情仍在逐渐恶化,最终导致致命的多器官衰竭。本病例强调了 CAPS 的不可预测性和侵袭性,以及当前管理策略的局限性。本病例强调了提高对 CAPS 患者的认识和早期积极治疗的必要性。该病例还强调了持续研究更有效治疗方法的重要性,以及多学科方法在管理此类复杂病例中的潜在益处。早期识别和干预对于改善 CAPS 患者的预后和疗效仍然至关重要。
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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审稿时长
7 weeks
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