Jacomacci Willian Pecin, Veloso Perdigão João Paulo, Veltrini Vanessa Cristina, Farah Gustavo Jacobucci, Tolentino Elen Souza, Vessoni Iwaki Lilian Cristina, Iwaki Filho Liogi
Gen Dent. 2017 Jan-Feb;65(1):28-32.
The purpose of this case report is to describe a previously unpublished association between focal cemento-osseous dysplasia (FCOD) and an aneurysmal bone cyst (ABC) and review the literature with regard to associated benign fibro-osseous lesions and cysts. A 41-year-old woman without a history of trauma presented with asymptomatic swelling in the right side of the mandible. Radiographs of the region revealed a unilocular radiolucent area with radiopaque foci. After aspiration of the lesion was positive for serosanguineous fluid, complete excision of the lesion was performed. Microscopic examination revealed a hybrid ABC and FCOD. The 12-month follow-up showed significant bone repair and no signs of recurrence. A review of the English-language literature from 1980 to 2012 revealed 1 retrospective study, 4 case series, and 18 single-case reports on the topic of cemento-osseous dysplasias, fibro-osseous lesions, and aneurysmal bone cysts. Of 59 cases, none reported an association between an ABC and FCOD. Although fibro-osseous lesions do not require intervention, surgical excision is recommended when they are associated with cysts. This case, in which an ABC and FCOD were associated, reinforces the need for a careful diagnostic process in radiographically mixed lesions that respond positively to aspiration biopsy.
本病例报告的目的是描述一种此前未发表的局灶性骨化纤维发育异常(FCOD)与动脉瘤样骨囊肿(ABC)之间的关联,并回顾有关相关良性纤维骨性病变和囊肿的文献。一名无创伤史的41岁女性,下颌右侧出现无症状肿胀。该区域的X线片显示一个单房性透光区伴有不透光灶。病变抽吸物为血性浆液后,对病变进行了完整切除。显微镜检查显示为ABC与FCOD的混合型。12个月的随访显示有明显的骨修复,且无复发迹象。对1980年至2012年的英文文献进行回顾,发现有1项回顾性研究、4个病例系列以及18篇关于骨化纤维发育异常、纤维骨性病变和动脉瘤样骨囊肿主题的单病例报告。在59例病例中,无一例报告ABC与FCOD之间存在关联。虽然纤维骨性病变无需干预,但当它们与囊肿相关时,建议手术切除。本病例中ABC与FCOD相关,这强化了对于影像学表现为混合型且对穿刺活检呈阳性反应的病变进行仔细诊断的必要性。