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Three-Dimensional Bone Extracellular Matrix Model for Osteosarcoma
Published on: April 12, 2019
Advanced osteosarcoma of the maxilla: a case report
Márcio Bruno Amaral1, Icaro Buchholz, Belini Freire-Maia
1Oral and Maxillofacial Surgery, Baleia Hospital, School of Dentistry, Pontifícia Universidade Católica de Minas Gerais, Belo Horizonte, MG, Brazil.
Medicina Oral, Patologia Oral Y Cirugia Bucal
|August 1, 2008
Summary
This case report details an advanced osteosarcoma of the maxilla, a rare jaw tumor. Despite initial misdiagnosis as fibrous dysplasia, the aggressive cancer led to rapid progression and patient death.
Area of Science:
- Oncology
- Pathology
- Oral and Maxillofacial Surgery
Background:
- Osteosarcomas are malignant bone tumors characterized by osteoid production by mesenchymal cells.
- While common in long bones, osteosarcoma of the jaw (JOS) is rare, typically presenting with lower metastasis rates and better prognosis.
- Delayed diagnosis in JOS can lead to advanced tumors and poorer outcomes.
Observation:
- A 38-year-old woman with a history of recurrent fibrous dysplasia presented with facial swelling, lip ulceration, and palate swelling.
- Computed tomography revealed a large mass in the right maxilla extending to the orbit and maxillary sinus.
- Microscopic examination of an incisional biopsy confirmed osteosarcoma with osteoid and chondroid formation.
Findings:
- The patient was diagnosed with advanced osteosarcoma of the maxilla.
- Despite oncologic treatment recommendations, the tumor exhibited uncontrollable local spread.
- The patient succumbed to the disease six months post-diagnosis.
Implications:
- This case highlights the critical importance of early and accurate diagnosis of jaw tumors to prevent advanced disease.
- It underscores the aggressive potential of osteosarcoma of the jaw, even with a generally better prognosis.
- Accurate histopathological evaluation is crucial for differentiating rare jaw malignancies from benign conditions like fibrous dysplasia.