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.
Original language | English (US) |
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Pages (from-to) | 638-640 |
Number of pages | 3 |
Journal | Journal of Neurosurgery: Pediatrics |
Volume | 15 |
Issue number | 6 |
DOIs | |
State | Published - Jun 2015 |
Externally published | Yes |
Keywords
- Klippel-Trenaunay-Weber syndrome
- Oncology
- Osteoblastoma
- Pediatric
- Rib
- Spine
ASJC Scopus subject areas
- Surgery
- Pediatrics, Perinatology, and Child Health
- Clinical Neurology