Fibrous dysplasia associated with peripheral giant cell granoluma in maxilla in a young patient, a case report of rare hybrid lesion.

IF 0.9 Q4 ONCOLOGY
Abbas Karimi, Samira Derakhshan, Mahboube Hasheminasab, Sheida Kordi
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Abstract

Benign fibro-osseous lesions are a diverse range of entities that have distinct clinical and radiographic features. They can occur as solitary lesions or concomitant with other pathologies as hybrid lesions. Fibrous dysplasia (FD) accompanied by central giant cell granuloma (CGCG), peripheral giant cell granuloma (PGCG) or peripheral ossifying fibroma (POF) as hybrid lesions, is reported very rarely in the literature. Although we were unable to find any reports of FD with PGCG as a hybrid lesion. Fibro-osseous lesions have certain histopathological features in common with PGCG including multinucleated giant cells. Here we report a 28 year old female with a painless, slow growing and pedunculated swelling of the maxilla for 18 months. Differential diagnosis consisted of FD, cemento-ossifying fibroma (COF), chondrosarcoma and probable PGCG considering radiographic and clinical investigations. Histopathologic findings revealed PGCG and FD as a hybrid lesion. The combination of PGCG and FD has not been reported in the literature so far.

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年轻患者上颌骨纤维发育不良伴外周巨细胞肉芽肿1例,为罕见的混合型病变。
良性纤维骨性病变是多种多样的实体,具有不同的临床和影像学特征。它们可以作为单独的病变发生,也可以作为混合病变与其他病理同时发生。纤维结构不良(FD)合并中央巨细胞肉芽肿(CGCG)、外周巨细胞肉芽肿(PGCG)或外周骨化纤维瘤(POF)为混合型病变,文献报道甚少。虽然我们没有发现任何FD与PGCG作为混合性病变的报道。纤维骨性病变与PGCG有一定的组织病理学特征,包括多核巨细胞。我们在此报告一位28岁的女性患者,她的上颌骨出现无痛、生长缓慢和带蒂的肿胀,持续了18个月。鉴别诊断包括FD,骨质骨化纤维瘤(COF),软骨肉瘤和可能的PGCG结合影像学和临床检查。组织病理学结果显示PGCG和FD为混合型病变。迄今为止,PGCG与FD合用尚未见文献报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
15 weeks
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