# Pathological Study of a Case of Catastrophic Antiphospholipid Syndrome in a Patient With Gastrointestinal Bleeding

**Authors:** Brian Shih, Qi Zhang, Hao Li

PMC · DOI: 10.7759/cureus.82263 · Cureus · 2025-04-14

## TL;DR

This paper presents a rare case of catastrophic antiphospholipid syndrome in a patient with a history of APS who experienced severe complications and died despite treatment.

## Contribution

The study contributes a detailed clinical and pathological case report of CAPS with gastrointestinal bleeding as a presenting symptom.

## Key findings

- The patient exhibited multiorgan vascular occlusion confirmed by autopsy with microthrombi in cardiac, pulmonary, and cerebral tissues.
- The case illustrates the challenges in managing thrombosis risk during treatment of concurrent health issues in APS patients.
- The patient's condition deteriorated rapidly despite interventions including warfarin reversal and antibiotic therapy.

## Abstract

Catastrophic antiphospholipid syndrome (CAPS) is a very rare, life-threatening form of antiphospholipid syndrome (APS) characterized by multiorgan vascular occlusive events that occur rapidly in succession or simultaneously. Here, we describe a rare case of CAPS in a 67-year-old woman with a 26-year history of APS managed on therapeutic doses of warfarin presenting to hospital with a four-day history of melena secondary to gastrointestinal bleed. She was treated endoscopically, provided vitamin K for warfarin reversal, and started on dalteparin daily. During her course in hospital, she developed dyspnea and hypoxia with bilateral pleural effusions. The patient concurrently became increasingly hemodynamically unstable. She was treated with furosemide and broad-spectrum antibiotics but deteriorated, experienced cardiac arrest, and could not be successfully resuscitated. On autopsy, widespread microthrombi in cardiac, pulmonary, and cerebral tissues were identified and a diagnosis of CAPS was made. This case highlights the difficulty and importance of recognizing clinical manifestations of CAPS and balancing the risk for thrombosis when patients are undergoing treatment for concurrent serious health issues.

## Linked entities

- **Chemicals:** warfarin (PubChem CID 54678486), vitamin K (PubChem CID 5280483), furosemide (PubChem CID 3440)
- **Diseases:** Catastrophic antiphospholipid syndrome (MONDO:0018737), antiphospholipid syndrome (MONDO:0017278)

## Full-text entities

- **Genes:** FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, APOH (apolipoprotein H) [NCBI Gene 350] {aka B2G1, B2GP1, BG}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** GI bleed (MESH:D006471), fibrosis (MESH:D005355), inflammation (MESH:D007249), chest pain (MESH:D002637), death (MESH:D003643), epigastric pain (MESH:D010146), acute respiratory distress syndrome (MESH:D012128), myocardial injury (MESH:D009202), neoplasm (MESH:D009369), Cardiac involvement (MESH:D006331), cardiac arrest (MESH:D006323), NETs (MESH:C536657), myocardial infarction (MESH:D009203), cardiac decompensation (MESH:D006333), pneumonia (MESH:D011014), pulmonary embolism (MESH:D011655), autoimmune condition (MESH:D001327), infarct (MESH:D007238), aortic stenosis-regurgitation (MESH:D001022), melena (MESH:D008551), valve disease (MESH:D006349), necrosis (MESH:D009336), transient ischemic attacks (MESH:D002546), atherosclerosis (MESH:D050197), ventricular concentric hypertrophy (MESH:D024741), Trauma (MESH:D014947), APS (MESH:D016736), SVT (MESH:D013617), LA (MESH:C531622), anemia (MESH:D000740), syncope (MESH:D013575), pleural effusions (MESH:D010996), hypoxia (MESH:D000860), venous thromboembolism (MESH:D054556), vessel occlusion (MESH:C536223), pulmonary edema (MESH:D011654), cardiovascular disease (MESH:D002318), dyspnea (MESH:D004417), bleeding (MESH:D006470), AKI (MESH:D058186), platelet aggregation (MESH:D001791), DVT (MESH:D020246), fibrocalcific degeneration (MESH:D009410), motion (MESH:D009041), pulmonary emboli (MESH:D020766), interstitial lung disease (MESH:D017563), Multiorgan system failure (MESH:D051437), pulmonary or cerebral infarct (MESH:D054060), cardiomegaly (MESH:D006332), thrombosis (MESH:D013927)
- **Chemicals:** creatinine (MESH:D003404), furosemide (MESH:D005665), ceftriaxone (MESH:D002443), bilirubin (MESH:D001663), piperacillin-tazobactam (MESH:D000077725), eosin (MESH:D004801), warfarin (MESH:D014859), Daratumumab (MESH:C556306), vitamin K (MESH:D014812), rivaroxaban (MESH:D000069552), dalteparin (MESH:D017985), defibrotide (MESH:C036901), MSB (-), hematoxylin (MESH:D006416)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12077937/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12077937/full.md

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Source: https://tomesphere.com/paper/PMC12077937