下颌骨中央巨细胞肉芽肿的不寻常影像学表现

B. Admani, F. Siddiqui, Huda Ahmed, Marya Hameed
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摘要

中央巨细胞肉芽肿(CGCG)是一种罕见的颌骨良性骨性病变。我们提出的情况下,侵略性CGCG在一个16岁的男孩与5个月的历史面部肿胀和鼻塞。他被转介到放射科会诊,因为右半边脸有多个扩大的肿胀。据报道,肿胀发作隐匿,进展缓慢,与感觉异常、鼻溢液或全身症状无关联。口腔外检查显示右侧面部弥漫性肿胀,使鼻唇沟消失,造成面部不对称。面部及颈部计算机断层扫描(CT)显示右侧下颌支扩张性多室溶解性病变,累及髁突及硬腭。在颅底也发现了类似的病变。扫描显示内部有细微的分隔和内部磨砂玻璃雾。它还显示了几个牙根和周围软组织的受累。术前病变口内活检显示多核巨细胞,包括梭形和圆形细胞。鉴别诊断帮助确定病变为CGCG。本病例有助于证明CGCG在临床、放射学和组织病理学特征上的广泛差异,以及彻底检查对及时诊断的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An unusual radiological manifestation of a mandibular central giant cell granuloma
Central giant cell granuloma (CGCG) is an uncommon benign osseous lesion of the jaw. We present the case of an aggressive CGCG in a 16-year-old boy with a 5-month history of facial swelling and nasal obstruction. He was referred for a radiology consult for multiple expanding swellings on the right hemi-face. The swellings were reported to have an insidious onset, slow progression and no association with paresthesia, nasal discharge, or systemic symptoms. Extra oral examination revealed a diffuse swelling on the right side of the face which obliterated the nasolabial fold causing facial asymmetry. A face and neck computed tomography (CT) showed expansile multi loculated lytic lesions of the right mandibular ramus which involved the condyle and hard palate. Similar lesions were also found in the skull base. Scans showed fine internal septations and internal ground glass haze. It also revealed involvement of several teeth roots and surrounding soft tissues. A pre-operative intra-oral biopsy of the lesion revealed multinucleated giant cells, comprising of both spindle-shaped and round cells. Differential diagnosis helped determine the lesions as CGCG. This case helps to demonstrate the wide variation in the clinical, radiological, and histopathological features of CGCG and the importance of thorough investigation for timely diagnosis.
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