| Literature DB >> 27118743 |
Jordan Maureen Moxey1, Emma Victoria Low2, Alice Margaret Turner3.
Abstract
We present two cases of eosinophilic granulomatosis with polyangiitis occurring with α-1-antitrypsin deficiency, both PiSZ phenotype. The simultaneous occurrence of these two conditions has seldom been described in the literature, despite evidence of an association between α-1-antitrypsin deficiency and other forms of vasculitis. Both patients had pulmonary involvement and reported intermittent exacerbations of vasculitic symptoms. Both patients were managed on low-dose oral steroids and azathioprine remaining well with occasional exacerbations. It is important to consider whether there is an association between eosinophilic granulomatosis with polyangiitis and α-1-antitrypsin deficiency, as this may lead to more severe pulmonary symptoms during exacerbations. If a genetic association between the two conditions is found, clinicians should be aware of the possible need to screen for α-1-antitrypsin deficiency in appropriate patients. 2016 BMJ Publishing Group Ltd.Entities:
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Year: 2016 PMID: 27118743 PMCID: PMC4854129 DOI: 10.1136/bcr-2015-214118
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X