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一名患有克-特-韦综合征患者的小儿骨母细胞瘤罕见表现:病例报告

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

作者信息

Wallace Scott A, Ignacio Romeo C, Klugh Arnett, Gates Gregory, Henry Marion C W

机构信息

1Department of Neurosurgery, Walter Reed National Military Medical Center, Bethesda, Maryland; and.

4Surgery, Naval Medical Center San Diego, California.

出版信息

J Neurosurg Pediatr. 2015 Jun;15(6):638-40. doi: 10.3171/2014.11.PEDS13478. Epub 2015 Mar 13.

Abstract

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.

摘要

骨母细胞瘤是一种罕见的原发性骨肿瘤,通常表现为长骨或脊柱的疼痛性病变。文献中仅两次报道骨母细胞瘤与系统性纤维瘤病相关。作者报告了一例8岁疑似患有Klippel-Trenaunay-Weber综合征(一种罕见的系统性纤维瘤病综合征)的女孩病例,该女孩表现为无痛性胸肋病变,经检查发现是骨母细胞瘤。

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