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.

PubMed

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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