# Primary Antiphospholipid Syndrome Presenting With Life-Threatening Diffuse Alveolar Hemorrhage

**Authors:** João Casanova Pinto, Manuel G Costa, Beatriz Fernandes, Carlos Ramalheira

PMC · DOI: 10.7759/cureus.93814 · 2025-10-04

## TL;DR

A 33-year-old man with a life-threatening lung condition was diagnosed with antiphospholipid syndrome and successfully treated with corticosteroids and anticoagulation.

## Contribution

This case highlights APS as a rare but critical cause of diffuse alveolar hemorrhage and emphasizes the importance of early diagnosis and treatment.

## Key findings

- The patient's symptoms and lab results confirmed antiphospholipid syndrome as the cause of diffuse alveolar hemorrhage.
- High-dose corticosteroids and anticoagulation led to successful recovery and long-term remission.
- Early recognition and aggressive treatment improved outcomes in this life-threatening condition.

## Abstract

Antiphospholipid syndrome (APS)-associated diffuse alveolar hemorrhage (DAH) results from antiphospholipid-induced endothelial dysfunction, microvascular thrombosis, and complement activation. Management requires balancing thrombosis prevention and hemorrhage control. High-dose corticosteroids are the first-line therapy.

We report a case of a 33-year-old male presenting with progressive dyspnea, hemoptysis, and hypoxemia. Initial evaluation revealed thrombocytopenia, anemia, elevated inflammatory markers, and diffuse bilateral ground-glass opacities on a thoracic computed tomography, consistent with DAH. Autoimmune serology confirmed persistent positivity for lupus anticoagulant, anti-cardiolipin IgM, and anti-β2-glycoprotein-I IgM, fulfilling APS classification criteria. The patient developed respiratory failure, requiring mechanical ventilation and venovenous extracorporeal membrane oxygenation (VV-ECMO). High-dose corticosteroids were initiated, leading to gradual improvement. He was successfully extubated and discharged on long-term anticoagulation with warfarin. At four years of follow-up, he remains free of APS-related complications.

This case highlights the importance of recognizing APS as a cause of DAH, particularly in patients with unexplained pulmonary hemorrhage. Early diagnosis and aggressive therapy can improve outcomes.

## Linked entities

- **Chemicals:** warfarin (PubChem CID 54678486)
- **Diseases:** antiphospholipid syndrome (MONDO:0017278), diffuse alveolar hemorrhage (MONDO:0019540), respiratory failure (MONDO:0021113), anemia (MONDO:0002280), thrombocytopenia (MONDO:0002049)

## Full-text entities

- **Diseases:** APS (MESH:D016736), dyspnea (MESH:D004417), lupus anticoagulant (MESH:C531622), microvascular thrombosis (MESH:D017566), DAH (MESH:D006470), thrombosis (MESH:D013927), respiratory failure (MESH:D012131), hemoptysis (MESH:D006469), inflammatory (MESH:D007249), thrombocytopenia (MESH:D013921), endothelial dysfunction (MESH:D014652), hypoxemia (MESH:D000860), anemia (MESH:D000740)
- **Chemicals:** warfarin (MESH:D014859), antiphospholipid (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12580941/full.md

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Source: https://tomesphere.com/paper/PMC12580941