A case of recurrent autoimmune hemolytic anemia during remission associated with acute pure red cell aplasia and hemophagocytic syndrome due to human parvovirus B19 infection successfully treated by steroid pulse therapy with a review of the literature

The patient was a 47-year-old man diagnosed as having autoimmune hemolytic anemia (AIHA) in April 2011. He also had a congenital chromosomal abnormality, a balanced translocation. Treatment with prednisolone (PSL) 60 mg/day resulted in resolution of the AIHA, and the treatment was completed in Novem...

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Detalhes bibliográficos
Main Authors: Sekiguchi, Yasunobu, Shimada, Asami, Imai, Hidenori, Wakabayashi, Mutsumi, Sugimoto, Keiji, Nakamura, Noriko, Sawada, Tomohiro, Komatsu, Norio, Noguchi, Masaaki
Formato: Artigo
Idioma:Inglês
Publicado em: e-Century Publishing Corporation 2014
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4069955/
https://ncbi.nlm.nih.gov/pubmed/24966977
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