Literature DB >> 31384199

Hereditary afibrinogenemia and pulmonary-renal hydralazine-induced vasculitis.

Ginger Tsai-Nguyen1, Ariel M Modrykamien1, Arthur Bredeweg2.   

Abstract

Combined pulmonary-renal hydralazine-induced vasculitis is rare, and hereditary afibrinogenemia is also rare. We present a case of a 62-year-old man with a history of hereditary afibrinogenemia who presented with hemoptysis and hematuria. Although he had prior episodes of hemoptysis that resolved with repletion of fibrinogen levels, a hydralazine-induced vasculitis was the ultimate cause of his recurrent hemoptysis and hematuria. Hydralazine was held and after transfusion with cryoprecipitate, he was treated with prednisone and rituximab.

Entities:  

Keywords:  Afibrinogenemia; antineutrophil cytoplasmic antibodies; hematuria; hemoptysis; hydralazine-induced vasculitis; myeloperoxidase; proteinase-3 antibodies

Year:  2019        PMID: 31384199      PMCID: PMC6650231          DOI: 10.1080/08998280.2019.1619397

Source DB:  PubMed          Journal:  Proc (Bayl Univ Med Cent)        ISSN: 0899-8280


  1 in total

Review 1.  Hydralazine-Induced ANCA Associated Vasculitis (AAV) Presenting with Pulmonary-Renal Syndrome (PRS): A Case Report with Literature Review.

Authors:  Karim Doughem; Ayman Battisha; Omar Sheikh; Lakshmi Konduru; Bader Madoukh; Mohammed Al-Sadawi; Shakil Shaikh
Journal:  Curr Cardiol Rev       Date:  2021
  1 in total

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