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成釉细胞癌:尼日利亚一家教学医院病例的临床病理分析及文献综述

Ameloblastic carcinoma: a clinicopathologic analysis of cases seen in a Nigerian Teaching Hospital and review of literature.

作者信息

Soyele Olujide Oladele, Adebiyi Kehinde Emmanuel, Adesina Olufunlola Motunrayo, Ladeji Adeola Mofolouwake, Aborisade Adetayo, Olatunji Abiodun, Adeola Henry Ademola

机构信息

Department of Oral Maxillo-facial Surgery and Oral Pathology, Obafemi Awolowo University, Ile-Ife, Nigeria.

Department of Oral Pathology and Oral Medicine, Faculty of Dentistry, Lagos State University College of Medicine, Ikeja, Lagos, Nigeria.

出版信息

Pan Afr Med J. 2018 Nov 27;31:208. doi: 10.11604/pamj.2018.31.208.14660. eCollection 2018.

Abstract

INTRODUCTION

Ameloblastic carcinoma is a rare malignant odontogenic neoplasm that exhibits histological features of ameloblastoma in combination with cytological atypia. It may arise de novo or secondarily through malignant de-differentiation of pre-existing ameloblastoma or odontogenic cyst. Secondary ameloblastic carcinomas often results from repeated surgical intervention, which is a mainstay of odontogenic tumor management in resource limited settings. To date, relatively few cases of ameloblastic carcinomas have been reported and many cases have been misdiagnosed as ameloblastoma. This is due to its wide range of clinicopathological feature which range from indolent to aggressive. It may present as an aggressive ulcerated mass or as a simple cystic lesion; hence, it often challenging to delineate from its benign counterpart, ameloblastoma.

METHODS

this study reviewed the clinicopathological data on 157 cases of odontogenic tumors diagnosed over a 10 years period from the pathology archive of the Oral Pathology Unit of Obafemi Awolowo University Teaching Hospital Complex (OAUTHC), Ile-Ife, Nigeria.

RESULTS

of all these cases, we identified that 64.9% were Ameloblastomas, while 8.3% were ameloblastic carcinomas. Primary subtypes of ameloblastic carcinoma constituted 23.08%, while 69.23% of the cases were of the secondary subtype. We also found that the secondary subtype of ameloblastic carcinomas showed a higher mean duration value of 7.7 years. Most lesions were found in posterior mandible and presented with ulceration, perforation and ill-defined borders radiographically.

CONCLUSION

this study is among the few that have documented higher frequency of secondary ameloblastic carcinoma in the scientific literature.

摘要

引言

成釉细胞癌是一种罕见的恶性牙源性肿瘤,具有成釉细胞瘤的组织学特征并伴有细胞异型性。它可原发出现,也可由先前存在的成釉细胞瘤或牙源性囊肿经恶性去分化继发产生。继发性成釉细胞癌常因反复手术干预所致,而在资源有限的地区,手术是牙源性肿瘤治疗的主要手段。迄今为止,成釉细胞癌的报道病例相对较少,许多病例被误诊为成釉细胞瘤。这是由于其广泛的临床病理特征,从惰性到侵袭性不等。它可能表现为侵袭性溃疡肿块或单纯囊性病变;因此,将其与良性对应物成釉细胞瘤区分开来往往具有挑战性。

方法

本研究回顾了尼日利亚伊费奥巴费米·阿沃洛沃大学教学医院综合院区口腔病理科10年间诊断的157例牙源性肿瘤的临床病理资料。

结果

在所有这些病例中,我们发现64.9%为成釉细胞瘤,而8.3%为成釉细胞癌。成釉细胞癌的原发性亚型占23.08%,而69.23%的病例为继发性亚型。我们还发现,继发性成釉细胞癌亚型的平均病程值更高,为7.7年。大多数病变位于下颌骨后部,影像学表现为溃疡、穿孔和边界不清。

结论

本研究是科学文献中少数记录继发性成釉细胞癌较高发生率的研究之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06a2/6718272/970b240270df/PAMJ-31-208-g001.jpg

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