12岁儿童单囊性成釉细胞瘤与牙源性角化囊肿的组织病理学交叉1例并文献复习。

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S R Nagar, S Ali, M Katarni, S S Talkar
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引用次数: 0

摘要

目的:由于临床和影像学特征重叠,儿科颌骨病变经常呈现诊断挑战。背景:其中,单囊性成釉细胞瘤(UA)和牙源性角化囊肿(OKC)是两种不同的牙源性实体,具有不同的生物学行为和复发风险。然而,少数病例可能表现出两者的组织病理学特征,使最终诊断和治疗复杂化。病例描述:本文报告一名12岁男孩,根据临床和影像学分析,其下颌病变临床提示为含牙囊肿。然而,去核囊性病变的组织病理学检查显示为腔内单囊性成釉细胞瘤,部分区域表现为牙源性角化囊肿的特征。讨论:这种不寻常的组合引起了重要的诊断和治疗考虑,特别是在儿童中,长期预后和复发风险必须仔细权衡。结论:该病例强调了组织病理学评估和临床病理相关性在儿科人群中这类模糊病变的关键作用,因为它有助于拓宽目前对牙源性囊性病变的理解,以获得适当的治疗和结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Histopathological crossover between unicystic ameloblastoma and odontogenic keratocyst in 12-year-old: a case report with literature review.

Aim: Pediatric jaw lesions often present diagnostic challenges due to overlapping clinical and radiographic features.

Background: Among these, unicystic ameloblastoma (UA) and odontogenic keratocyst (OKC) are two distinct odontogenic entities with differing biological behaviors and recurrence risk. However, a few cases may exhibit histopathological features of both, complicating definitive diagnosis and management.

Case description: This paper presents a case of a 12-year-old boy with a mandibular lesion clinically suggestive of a dentigerous cyst based on clinical and radiographical analysis. However, histopathological evaluation of the enucleated cystic lesion revealed intraluminal unicystic ameloblastoma, with some areas showing features of odontogenic keratocyst.

Discussion: This unusual combination raises important diagnostic and therapeutic considerations, particularly in children where long-term outcomes and recurrence risk must be weighed carefully.

Conclusion: The case emphasizes the critical role of histopathological evaluation and clinicopathological correlation of such ambiguous lesions in the pediatric population as it helps to broaden the current understanding of odontogenic cystic lesions for appropriate treatment and outcome.

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