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Acute myelogenous leukemia associated with Ollier disease
Author(s) -
White Matthew S.,
Martin Paul L.,
McLean Thomas W.
Publication year - 2008
Publication title -
pediatric blood and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.116
H-Index - 105
eISSN - 1545-5017
pISSN - 1545-5009
DOI - 10.1002/pbc.21050
Subject(s) - medicine , blood cancer , disease , leukemia , pathogenesis , cancer , pathology , oncology
Ollier disease is a rare disorder characterized by the presence of multiple enchondromas and a propensity to develop malignancies. We report the case of a 7‐year‐old Caucasian male with Ollier disease who developed acute myelogenous leukemia (AML). This report describes a patient with Ollier disease and AML and may offer a clue into the genetic pathogenesis of these disorders. Pediatr Blood Cancer 2008;50:645–646. © 2006 Wiley‐Liss, Inc.
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