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伴有囊性变的颅面骨纤维发育不良——一项诊断挑战。

Craniofacial fibrous dysplasia with cystic degeneration - A diagnostic challenge.

作者信息

Alves Fábio-Abreu, Matos Bruno-Henrique-Figueiredo, de Almeida Oslei-Paes, Carvalho Giovanna-Lopes

机构信息

DDS, PhD - Department of Stomatology, A.C.Camargo Cancer Center, São Paulo, Brazil.

DDS, PhD student - Department of Stomatology, School of Dentistry, University of São Paulo, São Paulo, Brazil.

出版信息

J Clin Exp Dent. 2023 Sep 1;15(9):e781-e786. doi: 10.4317/jced.60736. eCollection 2023 Sep.

DOI:10.4317/jced.60736
PMID:37799754
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10550077/
Abstract

Benign fibro-osseous lesions with cystic degenerations have been scarcely reported in craniofacial bones and its unusual characteristics pose a diagnostic challenge. Here, we report a case of craniofacial fibrous dysplasia presenting a large cystic degeneration. A 55-year-old woman had a history of pain, slight asymmetry on the zygomatic region and ocular pressure. Computed tomography revealed on the right side, multiple craniofacial bones showing a ground glass aspect, associated with an extensive hypodense, unilocular, well circumscribed lesion in the maxilla, and smaller lesions in the sphenoid bone. After a surgical procedure performed in another service, there was a complete improvement in symptoms, and after 1 year, the patient remains stable, with no changes. In the literature review, thirty-three reported cases of the same association in the craniofacial region were found. The main symptoms were sudden increase in the lesion and pain, and the indication of intervention in cystic lesions was only indicated in symptomatic cases or functional deficit. The knowledge of the possibility of the association of benign fibro-osseous lesions and cystic degenerations in craniofacial bones is essential to perform a correct diagnosis and treatment for these patients, consequently avoiding unnecessary procedures. Craniofacial fibrous dysplasia, Fibrous dysplasia, Benign fibro-osseous lesions, Cystic degeneration.

摘要

伴有囊性退变的良性纤维-骨病变在颅面骨中鲜有报道,其不寻常的特征带来了诊断挑战。在此,我们报告一例呈现巨大囊性退变的颅面骨纤维结构不良病例。一名55岁女性有疼痛病史,颧区轻度不对称及眼压异常。计算机断层扫描显示右侧多块颅面骨呈磨玻璃样外观,伴有上颌骨广泛的低密度、单房、边界清晰的病变,以及蝶骨的较小病变。在另一科室进行手术后,症状完全改善,1年后患者情况稳定,无变化。在文献回顾中,发现了33例颅面区相同关联的报道病例。主要症状为病变突然增大和疼痛,囊性病变的干预指征仅适用于有症状的病例或功能缺损。了解颅面骨中良性纤维-骨病变与囊性退变相关的可能性对于正确诊断和治疗这些患者至关重要,从而避免不必要的手术。颅面骨纤维结构不良、纤维结构不良、良性纤维-骨病变、囊性退变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5e8/10550077/738a959a8ba6/jced-15-e781-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5e8/10550077/00e604cbbba6/jced-15-e781-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5e8/10550077/7c68bb41e5de/jced-15-e781-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5e8/10550077/738a959a8ba6/jced-15-e781-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5e8/10550077/00e604cbbba6/jced-15-e781-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5e8/10550077/7c68bb41e5de/jced-15-e781-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5e8/10550077/738a959a8ba6/jced-15-e781-g003.jpg

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