The treatment of immune-mediated hemolytic anemia (IHA) complicating hem atopoietic stem cell transplantation (HSCT) is often unsatisfactory. We report a case of IHA which occurred after T-and B-cell depleted unrelated donor HSCT carried out for mucopolysaccharidosis type I-H (Hurler syndrome) which was successfully treated with anti-CD20+ monoclonal antibody.

Corti, P., Bonanomi, S., Vallinoto, C., Balduzzi, A., Uderzo, C., Cazzaniga, G., et al. (2003). Rituximab for immune hemolytic anemia following T- and b-cell-depleted hematopoietic stem cell transplantation. ACTA HAEMATOLOGICA, 109(1), 43-45 [10.1159/000067271].

Rituximab for immune hemolytic anemia following T- and b-cell-depleted hematopoietic stem cell transplantation

Balduzzi A;Cazzaniga G;
2003

Abstract

The treatment of immune-mediated hemolytic anemia (IHA) complicating hem atopoietic stem cell transplantation (HSCT) is often unsatisfactory. We report a case of IHA which occurred after T-and B-cell depleted unrelated donor HSCT carried out for mucopolysaccharidosis type I-H (Hurler syndrome) which was successfully treated with anti-CD20+ monoclonal antibody.
Articolo in rivista - Articolo scientifico
Hematopoietic stem cell transplantation; Hurler syndrome; Immune hemolytic anemia; Storage diseases;
English
2003
109
1
43
45
none
Corti, P., Bonanomi, S., Vallinoto, C., Balduzzi, A., Uderzo, C., Cazzaniga, G., et al. (2003). Rituximab for immune hemolytic anemia following T- and b-cell-depleted hematopoietic stem cell transplantation. ACTA HAEMATOLOGICA, 109(1), 43-45 [10.1159/000067271].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/395700
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