# The use of bilateral orthotopic lung transplantation in the management of acute severe drug-induced interstitial lung disease: A case report

**Authors:** Derek K. Afflu, Brittany A. Cody, Elizabeth Lendermon, Pablo G. Sanchez

PMC · DOI: 10.1016/j.jhlto.2024.100108 · 2024-05-10

## TL;DR

A young man with a history of COVID-19 developed severe lung disease from a medication and required a double lung transplant.

## Contribution

This case report highlights bilateral orthotopic lung transplantation as a potential treatment for severe drug-induced interstitial lung disease.

## Key findings

- The patient developed aggressive respiratory failure from trimethoprim-sulfamethoxazole (Bactrim) use.
- Bilateral orthotopic lung transplantation was performed due to extensive lung damage and fibrosis.
- Genetic susceptibility and prior COVID-19 may have contributed to rapid disease progression.

## Abstract

This case report presents a unique and severe manifestation of drug-induced interstitial lung disease (DIILD) in an 18-year-old male with a recent history of coronavirus disease 2019 (COVID-19) infection. The patient, treated with trimethoprim-sulfamethoxazole (Bactrim) for acne, developed a rapid and aggressively progressive respiratory failure and underwent bilateral orthotopic lung transplantation. Radiologic evaluation revealed extensive bilateral bronchiectasis, ground-glass opacities/consolidation, and fibrotic changes, with diffuse vascular thrombosis observed during explant pathology. Sulfonamides, particularly Bactrim, are implicated in DIILD, with male sex and pre-existing lung disease as common risk factors. The patient's simultaneous exposure to COVID-19 and genetic susceptibility to Bactrim allergy (human leukocyte antigen (HLA) B07:02 and HLA C07:02) may have contributed to the rapid progression of pulmonary fibrosis. Despite limited literature on lung transplantation for Bactrim-induced lung fibrosis, this case underscores its consideration as a viable treatment option in refractory cases.

## Linked entities

- **Genes:** HLAC_RS03480 (type II toxin-antitoxin system HicB family antitoxin) [NCBI Gene 7400175]
- **Chemicals:** trimethoprim-sulfamethoxazole (PubChem CID 358641), Bactrim (PubChem CID 5329)
- **Diseases:** coronavirus disease 2019 (MONDO:0100096), interstitial lung disease (MONDO:0015925), pulmonary fibrosis (MONDO:0002771)

## Full-text entities

- **Diseases:** bronchiectasis (MESH:D001987), DIILD (MESH:D017563), coronavirus disease 2019 (COVID-19) infection (MESH:D000086382), lung fibrosis (MESH:D005355), vascular thrombosis (MESH:D013927), pulmonary fibrosis (MESH:D011658), acne (MESH:D000152), allergy (MESH:D004342), respiratory failure (MESH:D012131), lung disease (MESH:D008171)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11935386/full.md

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Source: https://tomesphere.com/paper/PMC11935386