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12岁患者单囊性成釉细胞瘤与牙源性角化囊肿的组织病理学交叉:一例报告并文献复习

Histopathological crossover between unicystic ameloblastoma and odontogenic keratocyst in 12-year-old: a case report with literature review.

作者信息

Nagar S R, Ali S, Katarni M, Talkar S S

机构信息

Tata Memorial Centre, Mumbai, India.

出版信息

Eur Arch Paediatr Dent. 2025 Sep 16. doi: 10.1007/s40368-025-01112-8.

Abstract

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.

摘要

目的

由于临床和影像学特征重叠,小儿颌骨病变常常带来诊断挑战。

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病变,具有不同的生物学行为和复发风险。然而,少数病例可能同时表现出两者的组织病理学特征,使明确诊断和治疗复杂化。

病例描述

本文报告一例12岁男孩下颌病变病例,根据临床和影像学分析,临床上提示为含牙囊肿。然而,对摘除的囊性病变进行组织病理学评估发现,囊腔内为单囊性成釉细胞瘤,部分区域表现出牙源性角化囊肿的特征。

讨论

这种不寻常的组合引发了重要的诊断和治疗考量,尤其是在儿童中,必须仔细权衡长期预后和复发风险。

结论

该病例强调了组织病理学评估以及小儿人群中此类模糊病变的临床病理相关性的关键作用,因为它有助于拓宽目前对牙源性囊性病变的认识,以进行适当的治疗和获得良好预后。

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