| Literature DB >> 18321906 |
Suzanna C Jamison1, Stephen Brierre, Jon Sweet, Ben de Boisblanc.
Abstract
Severe emphysema developed in a white woman with a 26-pack-year history of tobacco use. Serum alpha(1)-antitrypsin levels were normal. A history of autoimmune hemolytic anemia, angioedema, low complement, and recurrent urticaria prompted an immunologic workup that ultimately led to a diagnosis of hypocomplementemic urticarial vasculitis syndrome. Treatment with oral prednisone and inhaled bronchodilators improved symptoms, but 4 months after diagnosis non-small cell lung cancer was discovered and she ultimately died. Hypocomplementemic urticarial vasculitis is an uncommon cause of precocious emphysema and has not previously been reported in a patient with bronchogenic carcinoma.Entities:
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Year: 2008 PMID: 18321906 DOI: 10.1378/chest.07-0942
Source DB: PubMed Journal: Chest ISSN: 0012-3692 Impact factor: 9.410