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首页> 外文期刊>European review for medical and pharmacological sciences. >Diagnosis and treatment of a rare case of adenomatoid odontogenic tumor in a young patient affected by attenuated familial adenomatosis polyposis (aFAP): case report and 5 year follow-up
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Diagnosis and treatment of a rare case of adenomatoid odontogenic tumor in a young patient affected by attenuated familial adenomatosis polyposis (aFAP): case report and 5 year follow-up

机译:一名年轻的家族性减毒性家族性腺瘤病息肉病(aFAP)患者的罕见腺瘤样牙源性肿瘤的诊断和治疗:病例报告和5年随访

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摘要

BACKGROUND: The adenomatoid odontogenic tumor (AOT) is a quite rare odontogenic tumor, with an incidence rate of approximately 12 cases/year worldwide. Attenuated familial adenomatous polyposis (aFAP) is a syndrome characterized by a significant risk to develop colon cancer. The aim of the paper is to describe a case never reported before in the literature: an AOT developed in a patient with aFAP; moreover, we want to show how it appears 5 years after surgery and after the regeneration of the eroded bone tissue, using the Platelet-Rich Fibrin (PRF) as filling material.
机译:背景:腺瘤样牙源性肿瘤(AOT)是一种非常罕见的牙源性肿瘤,全世界的发病率约为12例/年。家族性腺瘤性息肉病(aFAP)减弱是一种以发展为结肠癌的重大风险为特征的综合征。本文的目的是描述一种文献中从未报道过的病例:aFAP患者发生AOT;此外,我们想用富含血小板的纤维蛋白(PRF)作为填充材料来显示手术后5年以及受侵蚀的骨组织再生后的情况。

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