| Literature DB >> 30543928 |
Olga Tkachenko1, Sergey Lapin2, Alexey Maslyansky3, Valentina Myachikova3, Liya Mikhailova4, Boris Gilburd5.
Abstract
Relapsing Evans syndrome (ES) and systemic lupus erythematosus (SLE) with secondary antiphospholipid syndrome (APS) is very rare association. Coexistence of these syndromes is potentially fatal and require high-dose combined immunosuppressive therapy. We describe a case of successful use of Bortezomib and plasma exchange in a patient with ES and APS refractory to standard therapy. Thirty-two-year-old male who presented episodes of relapsing hemolytic anemia, pancytopenia and multiple thrombosis with positive direct and indirect antiglobulin test result, lupus anticoagulant and medium titer of anti-beta-2-glycoprotein 1 and anti-cardiolipin antibodies was diagnosed with ES and SLE with secondary APS. High-dose therapy by steroids and Cyclosporin A were started with temporary improvement. There was also no stable improvement with Rituximab and Cyclophosphamide. Bortezomib in combination with cyclosporine A and plasma exchange was introduced. He had stable improvement in hematological parameters with no evidence of relapse of hemolytic crisis or thrombosis during a follow-up for 1 year.Entities:
Keywords: Antiphospholipid syndrome; Bortezomib; Evans syndrome; Hemolysis; Thrombosis
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Year: 2018 PMID: 30543928 DOI: 10.1016/j.clim.2018.12.010
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969