An unusual presentation of pediatric osteoblastoma in a patient with Klippel-Trenaunay-Weber syndrome: case report

被引：2

作者：

Wallace, Scott A. ^{[1
]}

Ignacio, Romeo C. ^{[4
]}

Klugh, Arnett ^{[2
]}

Gates, Gregory ^{[3
]}

Henry, Marion C. W. ^{[4
]}

机构：

[1] Walter Reed Natl Mil Med Ctr, Dept Neurosurg, Bethesda, MD USA

[2] Naval Med Ctr San Diego, Dept Neurosurg, San Diego, CA 92134 USA

[3] Naval Med Ctr San Diego, Dept Pathol, San Diego, CA 92134 USA

[4] Naval Med Ctr San Diego, Dept Surg, San Diego, CA 92134 USA

来源：

JOURNAL OF NEUROSURGERY-PEDIATRICS | 2015年 / 15卷 / 06期

关键词：

osteoblastoma; pediatric; Klippel-Trenaunay-Weber syndrome; rib; spine; oncology; OSTEOID OSTEOMA; SPINE; PEG3; BONE;

D O I：

10.3171/2014.11.PEDS13478

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

Osteoblastoma is an uncommon primary bone tumor that usually presents as a painful lesion in a long bone or in the spine. Osteoblastoma has been reported only twice in the literature in conjunction with systemic fibromatosis. The authors report the case of an 8-year-old girl with suspected Klippel-Trenaunay-Weber syndrome, a rare syndrome of systemic fibromatosis, who presented with a painless thoracic rib lesion that was found to be an osteoblastoma.

引用

页码：638 / 640

页数：3

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