期刊
PEDIATRIC BLOOD & CANCER
卷 50, 期 3, 页码 645-646出版社
WILEY-LISS
DOI: 10.1002/pbc.21050
关键词
AML; child; leukemia; Ollier disease
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.
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