• 作者：H. Eddou ; C. Helissey ; J. Konopacki ; B. Souleau ; T. de Revel ; J.-V. Malfuson ; ^{jvmalf@free.fr}
• 关键词：Syndrome Evans ; Purpura thrombotique thrombocytopé ; nique ; Myé ; lodysplasie ; Manifestations immunologiques
• 刊名：La Revue de Medecine Interne
• 出版年：2012
• 期刊代码：237_02488663
• 类别：med
• 出版时间：March, 2012
• 卷：33
• 期：3
• 页码：155-158
• 文件大小：250 K

Introduction

Evans syndrome (ES) is characterized by the coexistence of an autoimmune hemolytic anemia (AIHA) and immune thrombocytopenic purpura (ITP). Despite being frequently evocated in the simultaneous presence of anemia and thrombocytopenia, this rare disease only accounts for 0.8 to 3.7%of patients with ITP or AIHA.

Case reports

We report three suspected cases of ES, diagnosed in the presence of thrombocytopenia and hemolytic anemia association, with a positive direct Coombs test in two patients. Standard ES treatment failure and occurrence of aditional features subsequently led to correct diagnosis to thrombotic thrombocytopenic purpura, myelodysplastic syndrome with AIHA, and ITP with hemorrhagic anemia, respectively.

Conclusion

Bicytopenias, even in an immunological context, are not sufficient to ascertain ES diagnosis. Our cases illustrate the diagnostic difficulties that may arise in daily practice, and induce over-diagnosis of this rare disease.