Primary Evans syndrome - case report

Abstract

Evans syndrome is a rare hematological disorder in which autoimmune hemolytic anemia and immune thrombocytopenia occur in the same patient. Patients usually have relapses and remissions. We report a female aged 32 years who presented with menorrhagia and purpuric rashes over her extremities. Investigations revealed thrombocytopenia and Coombs positive Autoimmune Hemolytic Anemia (AIHA) which was suggestive of Evans syndrome.

Authors and Affiliations

Vishnu Shankar H

Keywords

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  • EP ID EP418427
  • DOI -
  • Views 66
  • Downloads 0

How To Cite

Vishnu Shankar H (2017). Primary Evans syndrome - case report. International Journal of Allied Medical Sciences and Clinical Research, 5(2), 470-472. https://europub.co.uk/articles/-A-418427