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采用自体顶骨重建下颌骨成釉细胞纤维瘤:1例报告及文献复习

Ameloblastic Fibroma of the Mandible Reconstructed with Autogenous Parietal Bone: Report of a Case and Literature Review.

作者信息

Carroll Conor, Gill Mishaal, Bowden Eleanor, O'Connell John Ed, Shukla Rajeev, Sweet Chris

机构信息

Department of Oral and Maxillofacial Surgery, Alder Hey Children's NHS Foundation Trust, East Prescot Road, Liverpool L14 5AB, UK.

Department of Pathology, Alder Hey Children's NHS Foundation Trust, East Prescot Road, Liverpool L14 5AB, UK.

出版信息

Case Rep Dent. 2019 Jun 18;2019:5149219. doi: 10.1155/2019/5149219. eCollection 2019.

Abstract

Ameloblastic fibroma (AF) is a rare, slow-growing benign neoplasm, comprised of tissues of odontogenic origin. It constitutes 2% of odontogenic tumours, occurring at any age, but has a predilection to present in the first two decades of life. AF principally affects the posterior mandible. It is characterized by epithelial islands and cords immersed in ectomesenchyme that mimics the dental papilla and enamel organ but without actual hard tissue formation. Herein, we describe the case of a 6-year-old Caucasian male who presented to the Oral and Maxillofacial Department at Alder Hey Children's Hospital, Liverpool, UK, with a painless expansile mass in the left mandible which was diagnosed as a benign ameloblastic fibroma and subsequently enucleated and reconstructed with a parietal calvarial bone graft. A brief literature review and the issues surrounding diagnosis are discussed.

摘要

成釉细胞纤维瘤(AF)是一种罕见的、生长缓慢的良性肿瘤,由牙源性组织构成。它占牙源性肿瘤的2%,可发生于任何年龄,但好发于生命的前二十年。AF主要累及下颌骨后部。其特征是上皮岛和上皮条索浸润于外间充质中,类似牙乳头和牙釉质器官,但无实际硬组织形成。在此,我们描述一例6岁白种男性病例,该患者因左下颌无痛性膨胀性肿物就诊于英国利物浦奥尔德希儿童医院口腔颌面科,被诊断为良性成釉细胞纤维瘤,随后行肿物摘除术并用颅骨顶骨移植进行重建。本文还讨论了简要的文献综述及诊断相关问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5376/6604494/e4891c7e5dc0/CRID2019-5149219.001.jpg

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