Acute myelogenous leukemia associated with Ollier disease

被引：16

作者：

White, Matthew S. ^{[1
]}

Martin, Paul L. ^{[2
]}

McLean, Thomas W. ^{[1
]}

机构：

[1] Wake Forest Univ, Sch Med, Dept Pediat, Winston Salem, NC 27157 USA

[2] Duke Univ, Sch Med, Dept Pediat, Durham, NC USA

来源：

PEDIATRIC BLOOD & CANCER | 2008年 / 50卷 / 03期

关键词：

AML; child; leukemia; Ollier disease;

D O I：

10.1002/pbc.21050

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

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.

引用

页码：645 / 646

页数：2

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