口腔巨大化脓性肉芽肿伴面部皮肤血管瘤(Sturge-Weber综合征)。

T Ilgenli, T Canda, S Canda, T Unal, H Baylas
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引用次数: 0

摘要

这是一个病例报告的两名患者,年龄分别为26岁和22岁,谁遭受先天性血管瘤在他们的脸和明显的牙龈过度生长平行于口外病变。在手术前,通过专业的预防治疗和口腔卫生指导,卫生条件得到了改善。两个病例的组织学检查显示高度血管化的化脓性肉芽肿。其中一个病例与怀孕有关。这些患者可归类为斯特奇-韦伯综合征。术后治疗包括有效的菌斑控制和每3个月适当的口腔预防。随访2年、4年未见大面积牙龈增生复发。
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Oral giant pyogenic granulomas associated with facial skin hemangiomas (Sturge-Weber syndrome).

This is a case report of two patients, aged 26 and 22, who suffered from congenital hemangioma on their faces and pronounced gingival overgrowth localized parallel to extraoral lesions. Prior to surgical intervention the hygienic conditions were improved in several sessions by means of professional preventive treatment and oral hygiene instructions. Histologic examination of both cases revealed a highly vascularized pattern of pyogenic granuloma. One of the cases was associated with a pregnancy. These patients can be classified as Sturge-Weber syndrome. Postsurgical treatment consisted of efficient plaque control and adequate oral prophylaxis sessions every 3 months. The large gingival overgrowth was not observed to recur in 2 and 4 years, respectively, of follow-up.

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Regeneration of an osseous peri-implantitis lesion. Effect of a collagen membrane enriched with fibronectin on guided tissue regeneration in dogs. Evaluation of cellular response to collagen membranes enriched with fibronectin light and transmission electron microscope study. Central odontogenic fibroma--report of a case and review of the literature. Oral giant pyogenic granulomas associated with facial skin hemangiomas (Sturge-Weber syndrome).
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