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Pulmonary Infiltrates in a Non-Cystic Fibrosis Bronchiectasis Patient: A Case Report
Francesco Rocco Bertuccio1,2, Nicola Baio3, Simone Montini1,2
1Unit of Respiratory Disease, Cardiothoracic and Vascular Department, IRCCS Policlinico San Matteo, Viale Golgi 19, 27100 Pavia, Italy.
Abstract:
Background:Scedosporium apiospermum is a filamentous fungus increasingly recognized as an opportunistic pathogen in immunocompromised hosts, though rare infections in immunocompetent individuals with structural lung disease have been reported. Its diagnosis and management remain challenging due to non-specific clinical presentation and intrinsic resistance to multiple antifungal agents. Case Presentation: We report the case of a 66-year-old immunocompetent woman with idiopathic bilateral non-cystic fibrosis bronchiectasis, who presented with subacute cough and increased sputum production. Chest high-resolution CT revealed new subsolid and ground-glass infiltrates superimposed on stable bronchiectatic changes. Bronchoalveolar lavage (BAL) cultures isolated S. apiospermum as the sole pathogen. The patient was treated with oral voriconazole (200 mg BID) for 4 weeks, followed by a 4-week course of aerosolized amphotericin B. Clinical and radiological improvement was observed, and no relapse occurred during follow-up. Discussion: This case highlights the potential for S. apiospermum to cause clinically relevant pulmonary infection in structurally abnormal but immunocompetent lungs. Non-CF bronchiectasis may facilitate fungal colonization due to impaired mucociliary clearance and chronic mucus retention. Combined antifungal therapy involving systemic voriconazole and inhaled amphotericin B (though not yet standardized) was employed based on clinical rationale and the available literature, resulting in favorable outcomes. Conclusions:S. apiospermum pulmonary infection, although rare in immunocompetent hosts with bronchiectasis, should be considered in cases of new or persistent infiltrates. Early recognition and individualized antifungal strategies, including the potential role of inhaled agents, may improve clinical outcomes. This case reinforces the importance of multidisciplinary collaboration in the management of complex fungal infections in chronic airway disease.
Insights
Scedosporium apiospermum can cause lung infections in immunocompetent individuals with bronchiectasis. Early diagnosis and combined antifungal treatment, including inhaled therapies, improve outcomes for this rare pulmonary fungal infection.
Area of Science:
- Medical Mycology
- Pulmonology
- Infectious Diseases
Background:
- Scedosporium apiospermum is an emerging opportunistic fungal pathogen, primarily affecting immunocompromised individuals.
- Pulmonary infections by S. apiospermum are challenging due to non-specific symptoms and antifungal resistance.
- Structural lung diseases, like bronchiectasis, are increasingly recognized as risk factors, even in immunocompetent hosts.
Observation:
- A 66-year-old immunocompetent woman with non-cystic fibrosis bronchiectasis presented with cough and sputum.
- Chest CT showed new infiltrates superimposed on stable bronchiectasis.
- Bronchoalveolar lavage identified S. apiospermum as the sole causative agent.
Findings:
- The patient received a combination therapy of oral voriconazole and aerosolized amphotericin B.
- Clinical and radiological improvements were observed following treatment.
- No recurrence of infection was noted during the follow-up period.
Implications:
- This case underscores S. apiospermum's potential to cause significant pulmonary disease in immunocompetent individuals with underlying lung abnormalities.
- Non-cystic fibrosis bronchiectasis may predispose individuals to fungal colonization due to impaired airway clearance.
- Individualized treatment strategies, potentially including inhaled antifungals, are crucial for managing S. apiospermum pulmonary infections.
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