Cartilaginous Choristoma of the Oral Cavity: A Rare Presentation in the Nasopharynx.

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Case Reports in Medicine Pub Date : 2024-12-17 eCollection Date: 2024-01-01 DOI:10.1155/carm/4506082
Maryam Al-Ali, Anastasios Hantzakos
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Abstract

Objective: This case report describes a rare presentation of a cartilaginous choristoma of the oral cavity within the tonsillar fossa, emphasizing the importance of recognizing and differentiating this uncommon entity from more frequently encountered oral lesions. Methods: A comprehensive clinical and histopathological examination was conducted on a 30-year-old male patient who presented with a painless mass in the nasopharynx. An excisional biopsy was carried out, and a histopathological analysis was conducted to establish a definitive diagnosis. Results: Histopathological examination demonstrated a cartilaginous choristoma, characterized by the presence of mature hyaline cartilage surrounded by the connective tissue. The patient underwent surgical excision of the lesion, and follow-up assessments indicated a favorable postoperative outcome without recurrence. Conclusion: Cartilaginous choristomas in the oral cavity are exceedingly rare. Awareness of this entity is crucial for accurate diagnosis and appropriate management, as it can mimic other more common oral lesions. This case report contributes to the limited literature on oral cartilaginous choristomas and underscores the significance of considering this entity in the differential diagnosis of oral mucosal masses.

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口腔软骨脉络瘤:鼻咽部罕见的表现。
目的:本病例报告描述了一个罕见的扁桃体窝内的口腔软骨绒毛瘤,强调了识别和区分这种不常见的实体与更常见的口腔病变的重要性。方法:对一位30岁男性患者进行了全面的临床和组织病理学检查,他表现为鼻咽部无痛性肿块。进行了切除活检,并进行了组织病理学分析,以建立明确的诊断。结果:组织病理学检查显示为软骨性脉络瘤,其特征是结缔组织包围着成熟的透明软骨。患者接受手术切除病变,随访评估显示良好的术后结果,无复发。结论:口腔软骨脉络膜瘤极为罕见。意识到这个实体是至关重要的准确诊断和适当的管理,因为它可以模仿其他更常见的口腔病变。本病例报告补充了关于口腔软骨脉络瘤的有限文献,并强调了在口腔粘膜肿块鉴别诊断中考虑这一实体的重要性。
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来源期刊
Case Reports in Medicine
Case Reports in Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
1.70
自引率
0.00%
发文量
53
审稿时长
13 weeks
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