Infantile myofibromatosis: A case report and review of the literature

被引：0
|
作者：
Ang, P
Tay, YK
Walford, NQ
机构：
[1] Natl Skin Ctr, Singapore 1130, Singapore
[2] Singapore Gen Hosp, Dept Pathol, Singapore, Singapore
来源：
CUTIS | 2004年 / 73卷 / 04期
关键词：
D O I：
暂无
中图分类号：
R75 [皮肤病学与性病学];
学科分类号：
100206 ;
摘要：
Infantile myofibromatosis is a rare mesenchymal disorder of infancy and childhood characterized by the formation of tumors in the soft tissues, muscle, bone, and viscera. Disease limited to the soft tissues, muscle, and bone has a good prognosis, and excision is curative; however, visceral involvement may be fatal. We present a case of infantile myofibromatosis in a 1-year-old boy and review the literature.
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页码：229 / 231
页数：3
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