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成釉细胞纤维牙瘤

Ameloblastic fibro-odontoma.

作者信息

Surej Kumar L K, Manuel Suvy, Khalam Sherin A, Venugopal Kannan, Sivakumar T T, Issac Jyothi

机构信息

Department of Oral and Maxillofacial Surgery, PMS College of Dental Science and Research, Trivandrum, Kerala, India.

Department of Oral and Maxillofacial Pathology, PMS College of Dental Science and Research, Trivandrum, Kerala, India.

出版信息

Int J Surg Case Rep. 2014;5(12):1142-4. doi: 10.1016/j.ijscr.2014.11.025. Epub 2014 Nov 13.

Abstract

INTRODUCTION

Ameloblastic fibro-odontoma (AFO) is a quite rare, mixed odontogenic tumour generally seen in the early stages of life. Frequent signs of this tumour are asymptomatic swelling, delayed tooth eruption and mixed radiological appearance within well-defined borders. Management of the lesion includes enucleation of the tumour and long-term follow-up.

PRESENTATION OF CASE

A 10-year-old girl was referred to our oral and maxillofacial surgery clinic with an incidental radiological finding of radiopaque mass in the posterior region of maxilla. OPG showed unerupted tooth bud of upper right second molar and was being prevented from eruption by the odontome. Under general anaesthesia, the lesion was enucleated and the permanent right upper second molar tooth bud removed.

DISCUSSION

Mixed odontogenic tumours are a group of rare and interesting lesions which can mislead the clinician to variety of differential diagnosis. Adequate clinical and radiological investigations, proper surgical excison, accurate histopathological diagnosis, and long term follow up will ensure the right treatment plan for the patient.

CONCLUSION

The possibility of a mixed rare tumour should be kept in mind by the clinician where they deal with the swellings of posterior maxilla in children. Histological assessment revealed a final diagnosis of ameloblastic fibro-odontoma.

摘要

引言

成釉细胞纤维牙瘤(AFO)是一种非常罕见的混合性牙源性肿瘤,通常在生命早期出现。该肿瘤常见症状有无症状肿胀、牙齿萌出延迟以及在边界清晰的区域内呈现混合性放射学表现。病变的处理包括肿瘤摘除及长期随访。

病例介绍

一名10岁女孩因上颌后部区域偶然发现不透光肿物的放射学检查结果转诊至我们的口腔颌面外科诊所。全景片显示右上颌第二磨牙牙胚未萌出,且被牙瘤阻挡无法萌出。在全身麻醉下,摘除病变并移除右上颌第二恒磨牙牙胚。

讨论

混合性牙源性肿瘤是一组罕见且有趣的病变,可能会使临床医生进行多种鉴别诊断。充分的临床和放射学检查、恰当的手术切除、准确的组织病理学诊断以及长期随访将确保为患者制定正确的治疗方案。

结论

临床医生在处理儿童上颌后部肿胀时应考虑到混合性罕见肿瘤的可能性。组织学评估最终诊断为成釉细胞纤维牙瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdc3/4276268/340980fbd8dd/gr1.jpg

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