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Published on: January 22, 2021
A cystic fibrosis child with lung function decline
Ersilia Vita Fiscarelli1, Gabriella Ricciotti1, Martina Rossitto1
1Laboratory Department, Children's Hospital and Research Institute Bambino Gesù, Rome, Italy.
Insights
A rare fungal infection, Arthrographis kalrae, was identified in a child with cystic fibrosis (CF) experiencing a pulmonary exacerbation. This case highlights a previously undocumented lung infection in pediatric CF patients, emphasizing the diverse fungal biota in CF airways.
Area of Science:
- Medical Mycology
- Pediatric Pulmonology
- Infectious Diseases
Background:
- Cystic fibrosis (CF) patients face significant risks from respiratory infections, including bacterial and fungal pathogens.
- The respiratory tract in CF is known to harbor a diverse fungal community, contributing to disease progression.
Observation:
- A 7-year-old child with CF presented with a pulmonary exacerbation.
- Bronchoalveolar lavage fluid analysis revealed the presence of Arthrographis kalrae.
Findings:
- This case represents the first documented instance of Arthrographis kalrae lung infection in a pediatric patient with cystic fibrosis.
- The isolation of A. kalrae suggests its potential role as a pathogen in CF pulmonary exacerbations.
Implications:
- This finding expands the spectrum of fungal organisms implicated in cystic fibrosis lung disease.
- Further research is warranted to understand the clinical significance and management of Arthrographis kalrae infections in CF patients.
Abstract:
Respiratory infections are a major threat to cystic fibrosis patients. Besides bacteria, many fungi colonize the cystic fibrosis respiratory tract where an important fungal biota has been described. We report here the case of a 7-year-old cystic fibrosis child with pulmonary exacerbation and Arthrographis kalrae isolated from bronchoalveolar lavage fluid. To the best of our knowledge, this is the first reported case of lung infection due to Arhtrographis kalrae in a cystic fibrosis pediatric patient.
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