Anemia and hepatosplenomegaly as presenting features in a child with rickets and secondary myelofibrosis |
| |
Authors: | Gruner Barbara A DeNapoli Thomas S Elshihabi Said Britton Howard A Langevin Anne-Marie Thomas Paul J Weitman Steven D |
| |
Affiliation: | Department of Pediatrics, University of Texas Health Science Center, San Antonio, Texas, USA. |
| |
Abstract: | Anemia and hepatosplenomegaly are common reasons for referring a child to a pediatric hematologist or oncologist. Among the many causes for these findings is severe rickets, which has been shown to be associated with secondary myelofibrosis and myeloid metaplasia. The authors present the case of an infant with severe rickets and secondary myelofibrosis and review the differential diagnosis of hepatosplenomegaly from the viewpoint of the pediatric hematologist/oncologist. |
| |
Keywords: | |
本文献已被 PubMed 等数据库收录! |
|