| Literature DB >> 25818375 |
Pierina Sansinanea1, Sebastián Augusto Carrica2, Josefina Marcos3, Mercedes Argentina García3.
Abstract
A case is presented of a protein-losing enteropathy (PLE) as the initial manifestation of systemic lupus erythematosus (SLE) in a 17 year-old female patient, who presented with ascites, edema and hypoalbuminemia. The diagnosis of SLE was based on the presence of: malar rash, oral ulcers, thrombocytopenia, antinuclear antibodies, IgM anticardiolipin antibody, and lupus anticoagulant. Renal and liver diseases were ruled out. The PLE diagnosis was confirmed with fecal alpha 1-antitrypsin clearance. The PLE was refractory to different lines of immunosuppressive agents like glucocorticoids, cyclophosphamide, azathioprine, and cyclosporine, showing a satisfactory and sustained response with rituximab, allowing steroid sparing and long term remission.Entities:
Keywords: Enteropatía perdedora de proteínas; Lupus eritematoso sistémico; Protein-losing enteropathy; Refractario; Refractory; Rituximab; Systemic lupus erythematosus
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Year: 2015 PMID: 25818375 DOI: 10.1016/j.reuma.2015.01.009
Source DB: PubMed Journal: Reumatol Clin ISSN: 1699-258X