Chaudhary Mayur, Chaudhary Shweta Dixit
Department of Oral and Maxillofacial Pathology and Microbiology, S.M.B.T. Dental College and Hospital, Ghulewadi, Amrutnagar, Post Sangamner, Distt. Ahmednagar, India.
J Oral Maxillofac Pathol. 2012 May;16(2):233-8. doi: 10.4103/0973-029X.99075.
Tumors of jaw bones are among the most uncommon of all types of neoplasms. Osteosarcoma of jaw bones represents a distinct group of lesions from the conventional type commonly occurring in long bones. Nonetheless, our present knowledge of the tumor allows us to affirm that its clinical behavior and pathologic features differ markedly from those of its homolog in the long bones. The maxillary tumors show predilection for posterior portion of the alveolar process and the antrum, whereas the body is most commonly involved in the mandible followed, by angle, symphysis, and ascending ramus. We have reviewed around 300 cases of osteosarcoma of varied racial origin from PubMed indexed journals spanning from 1967 to 2010 and present their etiology, pathogenesis, features and treatment modalities.
颌骨肿瘤是所有肿瘤类型中最罕见的。颌骨骨肉瘤是一组与常见于长骨的传统类型不同的病变。尽管如此,我们目前对该肿瘤的了解使我们能够确定,其临床行为和病理特征与长骨中的同源肿瘤明显不同。上颌肿瘤好发于牙槽突后部和上颌窦,而下颌骨体最常受累,其次是下颌角、下颌联合和下颌升支。我们回顾了1967年至2010年PubMed索引期刊上约300例不同种族来源的骨肉瘤病例,并介绍了它们的病因、发病机制、特征和治疗方式。