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[单囊性成釉细胞瘤伴发德莱曼综合征]

[Unicystic ameloblastoma presenting in Delleman's syndrome].

作者信息

Gilon Y, Thonnart F

机构信息

Service de Chirurgie Maxillo-faciale, CHU de Liège, site Sart Tilman, Liège, Belgique.

Service de Chirurgie Orale et Maxillo-faciale, CHU de Liège, site Sart Tilman, Liège, Belgique.

出版信息

Rev Med Liege. 2017 Jul;72(7-8):344-348.

Abstract

Ameloblastoma is an odontogenic tumour that represents 1 % of oral tumours but 10 % of odontogenic tumours. Ameloblastoma is characterized by low and noiseless growth, that explains a lot of advanced forms. The tumour is known as benign with local malignity due to its locally invasive behaviour and its recurrence. The treatment choice remains complicated because of recurring nature and large resection in vital anatomical areas. The therapeutic approach will be based on size, anatomical localisation, histologic variants and anatomical complications. The treatment options should be discussed with the patient because of possible important morphological and functional sequelae.

摘要

成釉细胞瘤是一种牙源性肿瘤,占口腔肿瘤的1%,但占牙源性肿瘤的10%。成釉细胞瘤的特点是生长缓慢且无声,这解释了许多晚期病例的情况。由于其局部侵袭行为和复发,该肿瘤虽为良性但具有局部恶性特征。由于其复发性以及在重要解剖区域需要进行大范围切除,治疗方案的选择仍然很复杂。治疗方法将基于肿瘤大小、解剖位置、组织学变异和解剖学并发症。由于可能会出现重要的形态和功能后遗症,治疗方案应与患者进行讨论。

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