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上颌骨和下颌骨的异时性成釉细胞瘤:病例报告

Metachronous ameloblastomas in the maxilla and mandible: report of a case.

作者信息

Abu El-Naaj Imad, Emodi Omri, Peled Micha

机构信息

Department of Oral and Maxillofacial Surgery, Rambam Medical Centre, Bruce Rappoport Faculty of Medicine, Technion Institute of Technology, Haifa, Israel.

出版信息

J Craniomaxillofac Surg. 2005 Oct;33(5):349-51. doi: 10.1016/j.jcms.2005.04.009.

Abstract

Ameloblastoma is a locally aggressive tumour of odontogenic origin, with an unknown aetiology. Metachronous ameloblastoma in the maxilla and the mandible is rare. In this report, a case of a 63 year-old man is described with a solid ameloblastoma in the posterior part of the upper jaw. After surgical treatment, the patient returned 8 years later with a similar lesion in the anterior lower jaw. Both ameloblastomas were of the solid type but differed in their histological patterns. No evidence of recurrence was found in either of the surgical sites for the last 4 years.

摘要

成釉细胞瘤是一种起源于牙源性的局部侵袭性肿瘤,病因不明。上颌骨和下颌骨发生异时性成釉细胞瘤较为罕见。在本报告中,描述了一例63岁男性患者,其在上颌后部患有实性成釉细胞瘤。手术治疗后,患者8年后下颌前部出现类似病变。两个成釉细胞瘤均为实性类型,但组织学模式不同。在过去4年中,两个手术部位均未发现复发迹象。

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