# Catastrophic Antiphospholipid Syndrome: A Rare but Life‐Threatening Thrombotic Storm—A Case Report and Literature Review

**Authors:** Renee Morecroft, Jordan Phillipps, Vikas Majithia, Sehreen Mumtaz

PMC · DOI: 10.1155/crrh/8852169 · Case Reports in Rheumatology · 2026-03-02

## TL;DR

This paper reports a rare case of catastrophic antiphospholipid syndrome and highlights the challenges in diagnosing and managing this life-threatening condition.

## Contribution

The paper contributes a detailed case report and literature review on CAPS management, emphasizing rituximab's potential role in long-term treatment.

## Key findings

- A 60-year-old male with APS developed CAPS and was successfully managed with high-dose corticosteroids and rituximab.
- Rituximab therapy led to sustained symptomatic improvement over 10 months in the reported case.
- Early recognition and individualized treatment are crucial for managing CAPS due to its high mortality rate.

## Abstract

Catastrophic antiphospholipid syndrome (CAPS) is a rare, life‐threatening variant of antiphospholipid syndrome (APS) characterized by rapid, widespread thrombosis leading to multiorgan failure. Affecting less than 1% of APS patients, CAPS is associated with a high mortality rate of 30%–50%, necessitating prompt diagnosis and aggressive treatment. The mainstay of management includes anticoagulation, high‐dose glucocorticoids, and plasma exchange or intravenous immunoglobulins, with biologic therapies such as rituximab and eculizumab reserved for refractory cases. We report a case of a 60‐year‐old male with a history of triple‐antibody–positive APS complicated by recurrent diffuse alveolar hemorrhage (DAH), adrenal hemorrhage, chronic kidney disease, and superficial vein thrombosis. His condition progressed to CAPS approximately 5 years prior with a course complicated by heparin‐induced thrombocytopenia. His condition stabilized with high‐dose corticosteroids and rituximab therapy with sustained symptomatic improvement after 10 months of rituximab. This case highlights the complexity of CAPS diagnosis and management, in the context of DAH, emphasizing the importance of early recognition, multidisciplinary care, and individualized treatment strategies. Our patient’s prolonged disease stabilization with rituximab underscores its potential role in long‐term CAPS management. Further research is needed to refine treatment protocols and improve outcomes for this rare but life‐threatening condition.

## Linked entities

- **Diseases:** catastrophic antiphospholipid syndrome (MONDO:0018737), antiphospholipid syndrome (MONDO:0017278), diffuse alveolar hemorrhage (MONDO:0019540), chronic kidney disease (MONDO:0005300), heparin-induced thrombocytopenia (MONDO:0018048)

## Full-text entities

- **Genes:** F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}, APOH (apolipoprotein H) [NCBI Gene 350] {aka B2G1, B2GP1, BG}
- **Diseases:** coagulopathy (MESH:D001778), infections (MESH:D007239), HUS (MESH:D006463), atrial fibrillation (MESH:D001281), HELLP (MESH:D017359), thrombocytopenia (MESH:D013921), APS (MESH:D016736), livedo racemosa (MESH:D054068), lupus anticoagulant (MESH:C531622), vein thrombosis (MESH:D012170), Thrombotic (MESH:D013927), death (MESH:D003643), encephalopathy (MESH:D001927), Thrombotic Storm (MESH:C566109), TTP (MESH:D011697), Disseminated intravascular coagulation (MESH:D004211), purpura (MESH:D011693), Renal injury (MESH:D007674), heart failure (MESH:D006333), TMA (MESH:D057049), cardiac complications (MESH:D006331), Raynaud's phenomenon (MESH:D011928), multiorgan failure (MESH:D051437), malignancy (MESH:D009369), adrenal insufficiency (MESH:D000309), Pulmonary complications (MESH:D008171), adrenal hemorrhage (MESH:D014884), pulmonary edema (MESH:D011654), chronic kidney disease (MESH:D051436), inflammatory (MESH:D007249), trauma (MESH:D014947), skin necrosis (MESH:D012871), gout (MESH:D006073), small-vessel occlusion (MESH:D059345), neurologic symptoms (MESH:D009461), pulmonary embolism (MESH:D011655), ARDS (MESH:D012128), SLE (MESH:D008180), Hemolysis (MESH:D006461), DAH (MESH:D006470), autoimmune diseases (MESH:D001327), chest pain (MESH:D002637), hemoptysis (MESH:D006469), stroke (MESH:D020521), acute renal failure (MESH:D058186)
- **Chemicals:** rituximab (MESH:D000069283), Antiphospholipid (-), hydroxychloroquine (MESH:D006886), warfarin (MESH:D014859), Heparin (MESH:D006493), LMWH (MESH:D006495), steroids (MESH:D013256), eculizumab (MESH:C481642), phospholipid (MESH:D010743), methylprednisolone (MESH:D008775)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC12952281/full.md

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Source: https://tomesphere.com/paper/PMC12952281