# Decellularized Pulmonary Homograft Repair of Idiopathic Main Pulmonary Artery Aneurysm in SC Hemoglobinopathy

**Authors:** Michael Hikaru Mikami, Clara Mayumi Mikami, Lucas do Valle Ciccozzi, Stephanie Senna da Silva, Paulo Roberto Slud Brofman, Claudinei Collatusso

PMC · DOI: 10.1016/j.jaccas.2026.106933 · JACC Case Reports · 2026-02-13

## TL;DR

A 48-year-old man with a rare lung artery aneurysm and a blood disorder successfully underwent surgery using a decellularized tissue graft.

## Contribution

This case demonstrates the safe use of decellularized pulmonary homografts in treating pulmonary aneurysms with SC hemoglobinopathy.

## Key findings

- The decellularized pulmonary homograft was effective in aneurysm repair without thromboembolic complications.
- The patient's postoperative recovery and graft function support the potential of this technique in similar cases.
- SC hemoglobinopathy patients may benefit from this approach due to their increased vascular risks.

## Abstract

Pulmonary artery aneurysm is a rare and potentially fatal condition, often diagnosed incidentally. The lack of specific guidelines makes it difficult to define clear intervention criteria and the ideal reconstructive technique. Decellularized pulmonary homografts (DPHs) have emerged as a promising alternative, although they are still scarcely reported.

A 48-year-old previously healthy man presented with mediastinal widening on a routine chest x-ray. Work-up revealed an idiopathic main pulmonary aneurysm measuring 52 mm, associated with moderate pulmonary valve stenosis. He underwent aneurysm resection and valve replacement with a DPH (size 25). The immediate postoperative course was satisfactory, but he developed severe pneumonia and was incidentally diagnosed with SC hemoglobinopathy.

The use of a DPH was appropriate in this setting, particularly considering the patient's age and the presence of SC hemoglobinopathy, a condition associated with increased risk of pulmonary hypertension, thrombotic events, and vascular inflammation. Follow-up demonstrated a competent graft with no thromboembolic complications, reinforcing the potential benefit of this technique.

This case highlights the use of a DPH as a safe and effective surgical option for an idiopathic main pulmonary artery aneurysm, especially in patients with associated hematologic conditions, emphasizing the importance of strict follow-up and individualized therapeutic strategies.

## Linked entities

- **Diseases:** pulmonary hypertension (MONDO:0005149), pneumonia (MONDO:0005249)

## Full-text entities

- **Diseases:** vascular inflammation (MESH:D007249), pneumonia (MESH:D011014), DPH (MESH:C562815), pulmonary hypertension (MESH:D006976), aneurysm (MESH:D000783), thrombotic (MESH:D013927), pulmonary valve stenosis (MESH:D011666), Pulmonary artery aneurysm (MESH:D000071079), SC Hemoglobinopathy (MESH:D006453), thromboembolic (MESH:D013923), Idiopathic Main Pulmonary Artery (MESH:D065627)
- **Chemicals:** DPH (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC13008553/full.md

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Source: https://tomesphere.com/paper/PMC13008553