成釉性牙肉瘤1例报告。

Acta stomatologica Belgica Pub Date : 1993-09-01
O Corominas-Villafañe, R Cuestas-Carnero, O Corominas, H Gendelman
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引用次数: 0

摘要

成釉性牙肉瘤是一种极为罕见的牙源性恶性肿瘤。迄今为止,文献中仅报告了8例。病例12岁的西班牙裔美国男孩与成釉性牙肉瘤的下颌骨提出。患者以前诊断为良性成釉纤维瘤,后来转变为成釉性牙肉瘤。患者手术切除肿瘤后随访19年。影像学和临床检查证实无复发迹象。继续定期检查肿瘤是否复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ameloblastic odontosarcoma: report of a case.

Ameloblastic odontosarcoma is an extremely rare malignant odontogenic tumor. To date only 8 cases have been reported in the literature. The case of a 12-year-old Hispanic-American boy with ameloblastic odontosarcoma of the mandible is presented. The patient had a tumor diagnosed previously as benign ameloblastic fibroma that underwent transformation to ameloblastic odontosarcoma. The patient has been followed for 19 years since the surgical removal of the tumor. Radiographic and clinical examination confirm that there is no evidence of recurrence. Periodic examination for the reappearance of the tumor will be continued.

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