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Hemorrhagic cystitis (HC) is a complication of hematopoietic stem cell transplantation (SCT), occurring in 10% to 70% of transplant recipients [1]. Intensive preparative regimens, especially those including busulfan, high-dose cyclophosphamide or ifosfamide, allogeneic SCT, transplantation from unrelated donors, and graft-versus-host disease (GVHD) are all factors that may contribute to the development of HC [2-4].
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Rao et al. (2009) studied this question.
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