Literature DB >> 17577490

Osteogenic sarcoma of the jaw: a 10-year experience.

Rui Fernandes1, Nikolaos G Nikitakis, Alexander Pazoki, Robert A Ord.   

Abstract

BACKGROUND: Osteosarcomas (OS) of all sites account for approximately 40% to 60% of primary malignant bone tumors. About 10% of OS occur in the head and neck; most are located in the mandible or maxilla. Jaw lesions are diagnosed on average 2 decades later than their long bone counterparts, which have a peak incidence between the ages of 10 and 14 years. Head and neck OS are associated with a lower metastatic rate than long bone OS, and they have a better 5-year survival rate, ranging between 27% and 84%. PATIENTS AND METHODS: We present our experience at the Department of Oral and Maxillofacial Surgery, University of Maryland, Baltimore, MD, with 16 patients with OS of the jaw during a period from 1993 to 2003.
RESULTS: In a retrospective chart review, 16 cases of OS of the jaw were identified. Patients ranged in age from 14 to 51 years (mean age, 41 years). The gender distribution consisted of 10 females and 6 males, at a ratio of 1.6:1. Evaluation of site distribution revealed a more frequent occurrence in the mandible than in the maxilla (9 and 7 cases, respectively). The main histologic subtype was chondroblastic (8 cases), followed by osteoblastic (4 cases). According to histologic grading, 8 tumors were high grade, 1 intermediate, 5 low grade, and 2 unknown. Overall, the primary treatment modality consisted of surgery in all 14 patients treated at the University of Maryland; 2 patients opted for treatment at other institutions. Chemotherapy, consisting primarily of cisplatin and Adriamycin (doxorubicin hydrochloride; Pharmacia, Kalamazoo, MI), was used as adjuvant treatment in 4 cases of high-grade OS. Follow-up ranges from 14 months to 108 months (mean, 46 months). To date, of the 14 patients treated at our institution, 12 (86%) had no evidence of disease at last appointment, and 2 patients died of the disease.
CONCLUSION: In light of the rarity of this disease, this series represents a large single-center experience with OS of the jaw. Our data show an older patient population, different gender distribution, and higher survival rate compared with overall published reports.

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Year:  2007        PMID: 17577490     DOI: 10.1016/j.joms.2006.10.030

Source DB:  PubMed          Journal:  J Oral Maxillofac Surg        ISSN: 0278-2391            Impact factor:   1.895


  27 in total

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2.  Collision tumor of maxilla: a diagnostic dilemma.

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3.  The Utility of MDM2 and CDK4 Immunohistochemistry and MDM2 FISH in Craniofacial Osteosarcoma.

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4.  Multimodal treatment of craniofacial osteosarcoma with high-grade histology. A single-center experience over 35 years.

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6.  Prognostic factors for teenage and adult patients with high-grade osteosarcoma: an analysis of 240 patients.

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7.  Multimodality treatment of osteosarcoma of the jaw: a single institution experience.

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Review 8.  Unusual presentation of extranodal diffuse large B-cell lymphoma in the head and neck: description of a case with emphasis on radiographic features and review of the literature.

Authors:  A Buchanan; S Kalathingal; J Capes; Z Kurago
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9.  Gnathic osteosarcomas, experience of four institutions from Turkey.

Authors:  Fetin R Yildiz; Arzu Avci; Omür Dereci; Behcet Erol; Bulent Celasun; Omer Gunhan
Journal:  Int J Clin Exp Pathol       Date:  2014-05-15

10.  Massive recurrent chondroblastic osteosarcoma of maxilla: a rare case report.

Authors:  Dwarkadas Adwani; Anirudh Bhattacharya; Nitin Adwani; Rinku Adwani; Vijay W Sharma
Journal:  J Clin Diagn Res       Date:  2014-01-12
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