# Bilateral Spontaneous Pneumothorax in a Patient With Metastatic Leiomyosarcoma Receiving Pazopanib: A Case Report

**Authors:** Maria Konstantinidou, Christina Chrysanthi Theocharidou, Anastasia Dimaki, Christos Emmanouilides, Fotini Ampatzidou

PMC · DOI: 10.7759/cureus.82161 · Cureus · 2025-04-13

## TL;DR

A patient with metastatic leiomyosarcoma on pazopanib developed bilateral pneumothorax, leading to severe complications and death.

## Contribution

This case report highlights a rare but serious adverse event of bilateral pneumothorax associated with pazopanib therapy in a patient with lung metastases.

## Key findings

- The patient experienced bilateral pneumothorax requiring emergency interventions.
- The patient had a prior history of unilateral pneumothorax, suggesting a predisposition.
- The clinical outcome was poor, with neurological damage and eventual death due to septic shock.

## Abstract

Pneumothorax can be a rare but significant adverse event in patients with sarcoma and pulmonary metastases. This case report presents an instance of bilateral pneumothorax in a patient with metastatic leiomyosarcoma treated with pazopanib. A 74-year-old man with a history of grade 3 leiomyosarcoma and lung metastases was admitted with severe respiratory distress. He had been receiving pazopanib therapy following previous treatment with high-dose ifosfamide, doxorubicin, and radiotherapy. Imaging revealed bilateral pneumothorax, and the patient subsequently experienced respiratory arrest requiring immediate resuscitation measures including needle decompression followed by chest tube placement. The patient had experienced a unilateral pneumothorax two months prior to this presentation, which had resolved with standard interventions. While the bilateral pneumothorax eventually resolved after nine days of chest tube drainage, the patient exhibited no neurological recovery following the arrest, with brain imaging revealing bilateral cortical laminar necrosis. His clinical condition deteriorated significantly after 28 days in the intensive care unit (ICU), culminating in septic shock and death. This case highlights a serious pulmonary complication that can occur during the treatment of metastatic leiomyosarcoma, particularly in patients with lung metastases. The relationship between the development of pneumothorax and pazopanib therapy, along with the challenges in management and poor clinical outcome, merits consideration when treating similar patients.

## Linked entities

- **Chemicals:** pazopanib (PubChem CID 10113978), ifosfamide (PubChem CID 3690), doxorubicin (PubChem CID 31703)
- **Diseases:** leiomyosarcoma (MONDO:0005058), pneumothorax (MONDO:0002076)

## Full-text entities

- **Genes:** VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, FLT1 (fms related receptor tyrosine kinase 1) [NCBI Gene 2321] {aka FLT, FLT-1, VEGFR-1, VEGFR1}, KIT (KIT proto-oncogene, receptor tyrosine kinase) [NCBI Gene 3815] {aka C-Kit, CD117, MASTC, PBT, SCFR}, TXK (TXK tyrosine kinase) [NCBI Gene 7294] {aka BTKL, PSCTK5, PTK4, RLK, TKL}, KDR (kinase insert domain receptor) [NCBI Gene 3791] {aka CD309, FLK1, VEGFR, VEGFR2}, FLT4 (fms related receptor tyrosine kinase 4) [NCBI Gene 2324] {aka CHTD7, FLT-4, FLT41, LMPH1A, LMPHM1, PCL}
- **Diseases:** pleural fistula (MESH:D010995), renal cell carcinoma (MESH:D002292), septic shock (MESH:D012772), lung (MESH:D008171), sarcoma (MESH:D012509), metastatic disease (MESH:D000092182), tenderness (MESH:D063806), trauma (MESH:D014947), hypercapnia (MESH:D006935), Pneumothorax (MESH:D011030), air leak (MESH:D004618), necrosis (MESH:D009336), arrest (MESH:D006323), tumor (MESH:D009369), lung metastases (MESH:D009362), deformity (MESH:D009140), bronchial (MESH:D001982), respiratory arrest (MESH:D012131), death (MESH:D003643), respiratory distress (MESH:D012128), thoracic pain (MESH:D010146), contusion (MESH:D003288), pelvic mass (MESH:C536030), thoracic trauma (MESH:D013896), fistula (MESH:D005402), ischemia (MESH:D007511), pelvic disease (MESH:D000292), respiratory acidosis (MESH:D000142), cavitary lesions (MESH:C566924), dyspnea (MESH:D004417), ischemic (MESH:D002545), Leiomyosarcoma (MESH:D007890), cerebral hypoperfusion (MESH:D002547), hypoxemia (MESH:D000860), liver toxicity (MESH:D056486)
- **Chemicals:** trabectedin (MESH:D000077606), doxorubicin (MESH:D004317), sunitinib (MESH:D000077210), dacarbazine (MESH:D003606), ifosfamide (MESH:D007069), sorafenib (MESH:D000077157), Pazopanib (MESH:C516667), oxygen (MESH:D010100)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12076265/full.md

## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12076265/full.md

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Source: https://tomesphere.com/paper/PMC12076265