Khonsari R H, Corre P, Charpentier P, Huet P
Service de chirurgie maxillo-faciale et stomatologie, CHU, 1, place Alexis-Ricordeau, 44000 Nantes, France.
Rev Stomatol Chir Maxillofac. 2011 Apr;112(2):107-9. doi: 10.1016/j.stomax.2009.07.014. Epub 2011 Feb 18.
Maxillary sinus osteomas are rare benign tumours with a poorly documented clinical evolution. Their craniofacial localization may be part of a syndrome. We report a case of maxillary sinus osteoma associated to a mucocele and a cyst probably of dental origin, with no sign of associated Gardner syndrome.
A 52-year-old woman consulted for chronic maxillary sinusitis and an oral vestibular fistula. The CT-scan suggested a mucocele with reactive bone formation. Macroscopically, a pediculated bone tumour was found next to a mucocele, and to a cyst probably of dental origin. The anatomopathological examination led to a diagnosis of cancellous osteoma.
Several hypotheses have been made on the etiology of sinus osteomas. When identified, screening for Gardner's syndrome should be implemented because of the associated risk for colic malignancy.
上颌窦骨瘤是罕见的良性肿瘤,其临床演变记录较少。它们在颅面部的定位可能是一种综合征的一部分。我们报告一例与黏液囊肿和可能起源于牙齿的囊肿相关的上颌窦骨瘤病例,未发现加德纳综合征的迹象。
一名52岁女性因慢性上颌窦炎和口腔前庭瘘前来就诊。CT扫描提示有黏液囊肿伴反应性骨形成。肉眼可见,在黏液囊肿旁发现一个带蒂骨肿瘤,以及一个可能起源于牙齿的囊肿。解剖病理学检查诊断为松质骨瘤。
关于鼻窦骨瘤的病因有多种假说。一旦确诊,应进行加德纳综合征筛查,因为存在结肠恶性肿瘤的相关风险。