G. Longobardi, I. Pagano, U. Sisalli, Maurizio Foresti, V. Poddi
{"title":"Extraosseous Cemento-Ossifying Fibroma of the Cheek","authors":"G. Longobardi, I. Pagano, U. Sisalli, Maurizio Foresti, V. Poddi","doi":"10.3814/2009/493190","DOIUrl":null,"url":null,"abstract":"Background. Cemento-ossifying fibroma (COF) is a relatively rare tumor of the maxillary bones, classified among the fibro-osseous lesions Feller et al. (2004). The lesion that develops appears within the bone, although in some cases, it involves the soft tissues Kaufmann et al. (1999), Jung et al. (1999). In literature there is not report of COF in the thickness of the cheek. Methods. A 24-year-old Caucasian woman presented a hard mass of 1.5 cm in the thickness of the right cheek; no signs of damaged tissues were present. Radiographically all the mass appeared radiopaque as bone, and well demarcated with an evident capsule, without invasing the adjacent structures. The lesion was resected en bloc. Result. Pathological examination of the excised mass revealed an encapsulated cemento-ossifying fibroma that did not invade the adjacent tissues. The case was resolved with no complicance and with restitutio ad integrum. Conclusion. Typically, the unusual characterisitcs of a pathology get difficult as for its diagnosis and therapy. This is a case report of a rare cemento-ossifying fibroma of the cheek. Clinical and instrumental examinations exclude a malignant pathology and lead to an appropriate conservative surgical therapy. Only the histological examination confirmed the clinical diagnosis of extraosseous COF.","PeriodicalId":169134,"journal":{"name":"Scholarly Research Exchange","volume":"40 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2009-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Scholarly Research Exchange","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3814/2009/493190","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3
Abstract
Background. Cemento-ossifying fibroma (COF) is a relatively rare tumor of the maxillary bones, classified among the fibro-osseous lesions Feller et al. (2004). The lesion that develops appears within the bone, although in some cases, it involves the soft tissues Kaufmann et al. (1999), Jung et al. (1999). In literature there is not report of COF in the thickness of the cheek. Methods. A 24-year-old Caucasian woman presented a hard mass of 1.5 cm in the thickness of the right cheek; no signs of damaged tissues were present. Radiographically all the mass appeared radiopaque as bone, and well demarcated with an evident capsule, without invasing the adjacent structures. The lesion was resected en bloc. Result. Pathological examination of the excised mass revealed an encapsulated cemento-ossifying fibroma that did not invade the adjacent tissues. The case was resolved with no complicance and with restitutio ad integrum. Conclusion. Typically, the unusual characterisitcs of a pathology get difficult as for its diagnosis and therapy. This is a case report of a rare cemento-ossifying fibroma of the cheek. Clinical and instrumental examinations exclude a malignant pathology and lead to an appropriate conservative surgical therapy. Only the histological examination confirmed the clinical diagnosis of extraosseous COF.
背景。骨水泥骨化纤维瘤(cemento - ossification纤维瘤,COF)是一种较为罕见的上颌骨肿瘤,Feller et al.(2004)将其归类为纤维骨性病变。病变出现在骨内,尽管在某些情况下,它涉及软组织Kaufmann et al. (1999), Jung et al.(1999)。在文献中没有报道COF在脸颊的厚度。方法。24岁白人女性,右脸颊硬肿块,厚度1.5 cm;没有组织受损的迹象。x线片显示所有肿块像骨一样不透光,边界清晰,有明显的包膜,未侵犯邻近结构。病灶整体切除。结果。病理检查发现包被骨水泥骨化纤维瘤,未侵犯邻近组织。该案件在没有合规性的情况下得到了解决,并得到了赔偿和赔偿。结论。通常情况下,病理的不寻常特征使其诊断和治疗变得困难。这是一例罕见的骨水泥骨化纤维瘤的脸颊报告。临床和仪器检查排除恶性病理,导致适当的保守手术治疗。只有组织学检查证实了骨外COF的临床诊断。