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成釉细胞纤维瘤:一例罕见表现的病例报告,展示了诊断挑战。

Ameloblastic Fibroma: A Case Report of a Rare Presentation Illustrating a Diagnostic Challenge.

作者信息

Estrela Carlos, Furlan Tatiana, Carvalhosa Artur A, Cirilo Nicole T, Marcon Neumara, Bueno Mike, Vêncio Eneida F, Silva Brunno Santos De Freitas

机构信息

Department of Stomatologic Sciences, School of Dentistry, Federal University of Goiás, Goiânia, GO, Brazil.

Private Practice, Primavera Do Leste, MT, Brazil.

出版信息

Contemp Clin Dent. 2025 Apr-Jun;16(2):136-139. doi: 10.4103/ccd.ccd_291_24. Epub 2025 Jul 14.

DOI:10.4103/ccd.ccd_291_24
PMID:40799233
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12338470/
Abstract

This case report emphasizes the diagnostic role of cone-beam computed tomography (CBCT) in identifying a rare pediatric case of ameloblastic fibroma (AF), comprising approximately 2% of odontogenic tumors. The 10-year-old patient initially presented with painless left mandibular posterior gingival swelling, resembling radicular or dentigerous cysts in clinical and conventional radiographic assessments. However, CBCT revealed a distinct periapical radiolucency linked to deciduous molar roots and an unerupted premolar, exposing mandibular lingual plate thinning and buccal plate disruption. The lesion extended beyond the unerupted premolar's enamel-cementum junction, suggesting an odontogenic tumor. Subsequent biopsy and histopathological examination confirmed AF. CBCT played a pivotal role in evaluating the lesion's interaction with surrounding bone structures, guiding treatment decisions, and contributing to an accurate diagnosis. Successful lesion excision, deciduous tooth extraction, and a disease-free year-long follow-up underscore the significance of enhancing diagnostic precision and managing uncommon odontogenic pathologies like AF.

摘要

本病例报告强调了锥形束计算机断层扫描(CBCT)在诊断罕见的儿童成釉细胞纤维瘤(AF)病例中的作用,AF约占牙源性肿瘤的2%。该10岁患者最初表现为左下颌后牙龈无痛性肿胀,在临床和传统影像学评估中类似于根囊肿或含牙囊肿。然而,CBCT显示根尖周有明显的透射区,与乳牙牙根和一颗未萌出的前磨牙有关,显示下颌舌侧板变薄和颊侧板破坏。病变超出未萌出前磨牙的釉质-牙骨质界,提示为牙源性肿瘤。随后的活检和组织病理学检查证实为AF。CBCT在评估病变与周围骨结构的相互作用、指导治疗决策以及有助于准确诊断方面发挥了关键作用。病变成功切除、乳牙拔除以及长达一年的无病随访强调了提高诊断准确性和管理AF等罕见牙源性病变的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1207/12338470/8a2ede0d333a/CCD-16-136-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1207/12338470/8ecb5282b55a/CCD-16-136-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1207/12338470/308587e66e99/CCD-16-136-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1207/12338470/8a2ede0d333a/CCD-16-136-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1207/12338470/8ecb5282b55a/CCD-16-136-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1207/12338470/308587e66e99/CCD-16-136-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1207/12338470/8a2ede0d333a/CCD-16-136-g003.jpg

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本文引用的文献

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Pediatric Odontogenic and Maxillofacial Bone Pathology: A Global Analysis.儿科牙源性和颌骨骨病理学:全球分析。
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Ameloblastic fibroma: an uncommon entity.成釉细胞纤维瘤:一种罕见的病变。
BMJ Case Rep. 2013 Jul 9;2013:bcr2013010279. doi: 10.1136/bcr-2013-010279.
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