Evans syndrome after Allogenic Peripheral Hematopoietic Stem Cell transplantation in a child with Severe Acquired Aplastic Anemia: case report and literature review
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Author:
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GHOLAMREZA BAHOUSH, FATEMEH AFRASHTEH
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Abstract:
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Here we report our experience with a 13-year-old boy diagnosed with sever acquired aplastic anemia underwent full matched sibling donor Allogenic peripheral blood stem cell transplantation (PBSCT). After hematopoietic stem cell transplantation stem cell (HSCT), following acute graft versus host disease (aGVHD), autoimmune hemolytic anemia (AIHA) with together idiopathic thrombocytopenia (Evans syndrome) happened. Epstein-Barr virus (EBV) and Cytomegalovirus (CMV) infection was also detected. After treatment with prednisolone, IVIG and rituximab the patient was discharged in good general condition.
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Keyword:
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Evans syndrome, Allogenic Peripheral Hematopoietic Stem Cell transplantation, Severe Acquired Aplastic Anemia.
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EOI:
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-
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DOI:
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https://doi.org/10.31838/ijpr/2021.13.01.423
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