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Unrelated stem cell transplant for infantile idiopathic myelofibrosis
Authors:Jennifer Domm MD  Cassie Calder PNP  Becky Manes RN  MSN  Christine Crossno PharmD  Hernan Correa MD  Haydar Frangoul MD
Affiliation:1. Pediatric Hematology/Oncology, Vanderbilt University, Nashville, Tennessee;2. Pharmacy, Vanderbilt University, Nashville, Tennessee;3. Pathology, Vanderbilt University, Nashville, Tennessee
Abstract:Idiopathic myelofibrosis (IMF) is a rare disease in children that can present during infancy and have a protracted course. The only known curative approach for this disease in adult patients is allogeneic stem cell transplant. We present two cases of IMF during infancy that did not resolve with supportive care measures. Both patients underwent unrelated stem cell transplant with complete resolution of their hematologic manifestations and resolution of the bone marrow fibrosis. Pediatr Blood Cancer 2009;52:893–895. © 2009 Wiley‐Liss, Inc.
Keywords:idiopathic myelofibrosis  infant  unrelated donor stem cell transplant
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