一名患有克鲁宗综合征并伴有黑棘皮病的 13 岁男孩患骨水泥化纤维瘤的罕见病例

IF 0.4 Q4 DENTISTRY, ORAL SURGERY & MEDICINE
Yumi Kawaoka , Kazuya Yoshida , Yukitada Hyo , Naoko Yano , Takeshi Yoshida , Koki Moriyoshi
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引用次数: 0

摘要

骨化性纤维瘤(COF)是颌骨的一种纤维骨性病变。根据世界卫生组织(WHO)2017年组织学分类,它被定义为良性间充质牙源性肿瘤。COF是一种相对罕见的肿瘤,一般发生在成年女性的下颌磨牙区。在此,我们报告了一例对称发生在儿童双侧下颌前区的 COF。患者是一名患有克鲁宗综合征的 13 岁男孩。由于在全景X光片上发现双侧下颌骨前部有放射状病变,他被转诊至我院。计算机断层扫描显示双侧下颌骨前区有病变。病灶被完全切除,并进行了组织病理学检查,结果证实双侧病灶均为 COF。术后两年随访时没有发现复发迹象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rare case of cemento-ossifying fibroma in a 13-year-old boy with Crouzon syndrome with acanthosis nigricans

Cemento-ossifying fibroma (COF) is a fibro-osseous lesion of the jaw. It was defined as a benign mesenchymal odontogenic tumor according to the World Health Organization (WHO) histological classification of 2017. COF is a relatively rare tumor that generally occurs in the mandibular molar region of adult women. Herein, we report a case of COF that occurred symmetrically in the bilateral anterior mandibular regions of a child. The patient was a 13-year-old boy who had Crouzon syndrome. He was referred to our clinic because radiolucent lesions were detected in the bilateral anterior mandibular regions on panoramic radiography. Computed tomography revealed lesions in the bilateral mandibular anterior regions. The lesions were completely removed, and histopathological examinations were performed, which confirmed COF in bilateral lesions. There was no evidence of recurrence at the 2-year postoperative follow-up.

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CiteScore
0.80
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审稿时长
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