舌软骨绒毛瘤1例报告并复习

Q3 Dentistry
Oral Surgery Pub Date : 2023-09-10 DOI:10.1111/ors.12847
Rani Iani Costa Gonçalo, Hianne Cristinne de Morais Medeiros, Janaina Lessa de Moraes dos Santos, Julliany Taverny Sousa, Carolina Maria Campos, Lélia Maria Guedes Queiroz
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引用次数: 0

摘要

脉络瘤是指正常细胞或组织在异常位置的增生。口腔脉络瘤被认为是非常罕见的。目的报告1例舌背表面软骨组织瘤的临床及病理特点。病例报告一名72岁的妇女以舌头持续性病变主诉到牙科诊所就诊。患者报告病灶生长缓慢约3个月,该区域无外伤史。口腔内检查发现舌背表面结节状病变,黏膜颜色正常,硬度一致,无根植入,直径约1.5 cm。根据临床检查,考虑颗粒细胞瘤的诊断假设,并行切除活检证实。显微检查结果证实为软骨性脉络瘤。患者随访12个月,无复发迹象。结论本病例强调临床和组织病理学检查对正确诊断和治疗口腔脉络膜瘤的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A report of an unusual case of cartilaginous choristoma of the tongue and review
Abstract Background Choristomas consist of the proliferation of normal cells or tissue in an abnormal location. Oral choristomas are considered very rare. Aims The present study aims to report a case of dorsal tongue surface cartilaginous choristoma, with emphasis on its clinical and histopathological features. Case Report A 72‐year‐old woman attended a dental office with a chief complaint of a persistent tongue lesion. The patient reported that the lesion grew slowly for about 3 months, with no trauma history in the region. An intraoral examination revealed a nodular lesion on the dorsal tongue surface, normal mucosa coloration, firm consistency and sessile implantation, measuring approximately 1.5 cm in diameter. Based on the clinical examination, a diagnosis hypothesis of a granular cell tumour was considered, and an excisional biopsy was performed for confirmation. Given the microscopic findings, the histopathological diagnosis confirmed a cartilaginous choristoma. The patient has been under follow‐up for 12 months, with no signs of relapse. Conclusion This case highlights the importance of clinical and histopathological findings for the correct diagnosis and treatment of oral choristoma.
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来源期刊
Oral Surgery
Oral Surgery Medicine-Surgery
CiteScore
0.90
自引率
0.00%
发文量
80
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