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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease allergic bronchopulmonary aspergillosis
Comorbidity C0006267|bronchiectasis
Sentences 7
PubMedID- 21603163 If unrecognized or poorly treated, abpa leads to airway destruction, bronchiectasis, and/or pulmonary fibrosis, resulting in significant morbidity and mortality.
PubMedID- 23325730 [non-cf bronchiectasis with focus on allergic bronchopulmonary aspergillosis].
PubMedID- 24735832 A 23 patient study of abpa patients without bronchiectasis treated with inhaled corticosteroids showed subjective improvement but without complete control of asthma and median ige levels increased [193].
PubMedID- 22223932 Eventually, type 2 respiratory failure, cor pulmonale, and right heart failure develop in end-stage fibrotic abpa, with extensive bronchiectasis and fibrosis on hrct of the chest.
PubMedID- 22167396 Complications of abpa include bronchiectasis, typically central in distribution, and chronic pulmonary aspergillosis.
PubMedID- 24042528 Development of allergic bronchopulmonary aspergillosis with central bronchiectasis over a 10-year period: the need to recheck allergen sensitization.
PubMedID- 19207831 The prevalence of serological abpa (abpa without central bronchiectasis) was also higher in the asa group compared with the outpatient bronchial asthma group (45.4% vs.

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