Splenectomy for refractory Evans' syndrome associated with antiphospholipid antibodies:: report of two cases

被引:18
|
作者
Font, J
Jiménez, S
Cervera, R
Garcia-Carrasco, M
Ramos-Casals, M
Campdelacreu, J
Ingelmo, M
机构
[1] Hosp Clin Barcelona, Unitat Malaties Autoimmunes Sistem, Hosp Clin Barcelona,Inst Invest Biomed August Pi, Sch Med,Syst Autoimmune Dis Unit,Dept Med, E-08036 Barcelona, Spain
[2] Benemerita Univ Puebla, Sch Med, Dept Immunol, Puebla, Mexico
关键词
D O I
10.1136/ard.59.11.920
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The main haematological manifestations seen in patients with antiphospholipid antibodies (aPL) are thrombocytopenia, usually mild, and haemolytic anaemia with a positive Coombs test. Owing to the shared characteristics with idiopathic thrombocytopenic purpura, similar rules are followed in the treatment of these cytopenias. Two patients with severe aPL associated cytopenias, who required splenectomy after being refractory to steroids, immunosuppressive agents, and other treatments (intravenous gammaglobulin, danazol), are described, and previously reported cases are reviewed.
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收藏
页码:920 / 923
页数:4
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