Allergic bronchopulmonary aspergillosis (ABPA) is a syndrome seen in patien
ts with asthma and cystic fibrosis. It is characterized by chronic coloniza
tion of the airways with a ubiquitous fungus, Aspergillus fumigatus. The cl
inical expression of ABPA results from the complex interaction of chronic c
olonization of the airways with A. fumigatus, host factors allowing this co
lonization, and the host's genetically determined immune response. Clinical
ly the syndrome is characterized by recurrent episodes of wheezing, mucus p
roduction, pulmonary infiltrates, and elevated levels of serum IgE. Many pa
tients develop central bronchiectasis, and a subset will go on to endstage
fibrotic lung disease. It is thought that treatment will prevent this progr
ession. The mainstay of therapy remains oral corticosteroids.