A rare tumor of craniofacial bones in children: A pediatric chondroblasticosteosarcoma case with diagnostic and therapeutic problems

Citation
Km. Uysal et al., A rare tumor of craniofacial bones in children: A pediatric chondroblasticosteosarcoma case with diagnostic and therapeutic problems, PED HEM ONC, 18(2), 2001, pp. 147-152
Citations number
9
Categorie Soggetti
Pediatrics
Journal title
PEDIATRIC HEMATOLOGY AND ONCOLOGY
ISSN journal
08880018 → ACNP
Volume
18
Issue
2
Year of publication
2001
Pages
147 - 152
Database
ISI
SICI code
0888-0018(200103)18:2<147:ARTOCB>2.0.ZU;2-A
Abstract
Osteosarcoma of the cranial facial region is uncommon and only rarely invol ves the ethmoid or sphenoid bones. The authors report on an unusual case of a 17-year-old male presenting with chondroblastic osteosarcoma of the maxi llary, ethmoid, and sphenoid sinuses who remains well and disease-free at 4 6 months. He was treated with anterior craniofacial resection followed by p ostoperative radiotherapy to the sight of the primary tumor. He did not rec eive chemotherapy because of emerging hepatitis-B infection and vasculitis. The literature on extragnathic craniofacial osteosarcomas is reviewed with particular emphasis on treatment options of this rare tumor.