Unusual form of endobronchial aspergillosis in a patient with cystic fibrosis

Paul H. Sammut, Susan T. Howard, James Linder, John L. Colombo

Research output: Contribution to journalArticlepeer-review

9 Scopus citations


The isolation of Aspergillus fumigatus from airway secretions from patients with cystic fibrosis (CF) is common and usually denotes asymptomatic colonization or allergic broncho‐pulmonary aspergillosis (ABPA). A 12‐year‐old boy with CF acutely developed moderately severe symptoms of unremitting cough, fever, dyspnea, weight loss, and cyanosis. Chest radiographs demonstrated widespread unilateral infiltrates and volume loss. By bronchoscopy tenacious mucous plugs were seen occluding the left lower lobe bronchus. Cultures from sputum and sequential bronchoalveolar lavage grew Aspergillus fumigatus, but other significant criteria for diagnosing APBA were lacking. No improvement was seen with a 3 week course of systemic corticosteroid and antibiotic therapy. Treatment with amphotericin B and short‐term mechanical ventilation resulted in rapid resolution of all symptoms. This form of endobronchial aspergillosis has not been described previously. Pediatr Pulmonol. 1993; 16:69–73. © 1993 Wiley‐Liss, Inc.

Original languageEnglish (US)
Pages (from-to)69-73
Number of pages5
JournalPediatric Pulmonology
Issue number1
StatePublished - Jul 1993


  • Allergic broncho‐pulmonary aspergillosis
  • Aspergillus fumigatus
  • CF
  • amphotericin B

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Pulmonary and Respiratory Medicine


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