Literature DB >> 27118743

Rare case of eosinophilic granulomatosis with polyangiitis in two patients with α-1-antitrypsin deficiency (PiSZ).

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.

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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


  17 in total

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Journal:  Lancet       Date:  2015-05-27       Impact factor: 79.321

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Authors:  A Vaglio; C Buzio; J Zwerina
Journal:  Allergy       Date:  2013-01-18       Impact factor: 13.146

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Authors:  Ali Mota; Abbas Sahebghadam Lotfi; Ahmad-Reza Jamshidi; Saeed Najavand
Journal:  Rheumatol Int       Date:  2013-04-19       Impact factor: 2.631

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Authors:  Luc Mouthon; Bertrand Dunogue; Loïc Guillevin
Journal:  J Autoimmun       Date:  2014-02-12       Impact factor: 7.094

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  1 in total

1.  Fulminant hepatic failure in the setting of progressive ANCA-associated vasculitis associated with a rare alpha-1 antitrypsin phenotype, 'PiEE'.

Authors:  Ronald Reilkoff; Laurel Stephenson
Journal:  BMJ Case Rep       Date:  2018-03-28
  1 in total

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