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

Author:

Wallace Scott A.1,Ignacio Romeo C.2,Klugh Arnett3,Gates Gregory4,Henry Marion C. W.2

Affiliation:

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

2. Surgery, Naval Medical Center San Diego, California

3. Departments of Neurosurgery,

4. Pathology, and

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.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

General Medicine

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. A rare case of klippel-trenaunay syndrome presenting with chronic myeloid leukemia;The Turkish Journal of Pediatrics;2023

2. Cancer Risk in Klippel–Trenaunay Syndrome;Lymphatic Research and Biology;2019-12-01

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