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

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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.

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Wallace, S. A., Ignacio, R. C., Klugh, A., Gates, G., & Henry, M. C. W. (2015). An unusual presentation of pediatric osteoblastoma in a patient with Klippel-Trenaunay-Weber syndrome: Case report. Journal of Neurosurgery: Pediatrics, 15(6), 638–640. https://doi.org/10.3171/2014.11.PEDS13478

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