Chest
Volume 135, Issue 3, March 2009, Pages 805-826
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Global Medicine
Allergic Bronchopulmonary Aspergillosis

https://doi.org/10.1378/chest.08-2586Get rights and content

Allergic bronchopulmonary aspergillosis (ABPA) is an immunologic pulmonary disorder caused by hypersensitivity to Aspergillus fumigatus. Clinically, a patient presents with chronic asthma, recurrent pulmonary infiltrates, and bronchiectasis. The population prevalence of ABPA is not clearly known, but the prevalence in asthma clinics is reported to be around 13%. The disorder needs to be detected before bronchiectasis has developed because the occurrence of bronchiectasis is associated with poorer outcomes. Because many patients with ABPA may be minimally symptomatic or asymptomatic, a high index of suspicion for ABPA should be maintained while managing any patient with bronchial asthma whatever the severity or the level of control. This underscores the need for routine screening of all patients with asthma with an Aspergillus skin test. Finally, there is a need to update and revise the criteria for the diagnosis of ABPA. This review summarizes the advances in the diagnosis and management of ABPA using a systematic search methodology.

Section snippets

Epidemiology of ABPA

Aspergillus hypersensitivity (AH) is defined by the presence of an immediate-type cutaneous hypersensitivity to A fumigatus antigens, and it is the first step in the development of ABPA.24 Only a minority of patients with AH develop the complete clinical picture of ABPA.25 The population prevalence of ABPA in asthma, generally referred to as 1 to 2%,5, 13, 26, 27 is based on the inference of only three studies (one peer-reviewed and two non-peer-reviewed studies).28, 29 In the only

Conclusions

A high index of suspicion for ABPA should be maintained while managing any patient with bronchial asthma whatever the severity or the level of control. Host immunologic responses are central to the pathogenesis, and they are the primary determinants of the clinical, biologic, pathologic, and radiologic features of this disorder. ABPA may precede the clinical recognition of the disorder for many years or even decades, and it is often misdiagnosed as a variety of pulmonary diseases. Because a

Acknowledgment

The author wishes to thank Dr. Amanjit Bal, Assistant Professor, Department of Histopathology, PGIMER, Chandigarh for providing the histopathology photographs.

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