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口腔息肉作为一名儿童贝克威思-维德曼综合征的首发特征。

Oral polyp as the presenting feature of Beckwith-Wiedemann syndrome in a child.

作者信息

Kujan Omar, Raheel Syed Ahmed, King David, Iqbal Fareed

机构信息

Department of Oral and Maxillofacial Sciences, Al-Farabi Colleges, Riyadh, Saudi Arabia.

Al-Farabi Colleges, Riyadh, Saudi Arabia.

出版信息

BMJ Case Rep. 2015 Aug 30;2015:bcr2015210758. doi: 10.1136/bcr-2015-210758.

Abstract

Beckwith-Wiedemann syndrome (BWS) is a congenital growth disorder characterised by abdominal wall defects, macroglossia and somatic gigantism. A number of associated features, including gastrointestinal and urinary tract polyps, have been described, but there are no previous reports of oral polyps occurring in this syndrome. We describe the first case of BWS presenting with an oral polyp. Clinicians should be alert to the possibility of BWS if other features of the syndrome are present, in children with oral polyps.

摘要

贝克威思-维德曼综合征(BWS)是一种先天性生长障碍,其特征为腹壁缺损、巨舌症和躯体巨大症。已描述了许多相关特征,包括胃肠道和泌尿道息肉,但此前并无该综合征出现口腔息肉的报道。我们报告了首例伴有口腔息肉的BWS病例。对于患有口腔息肉的儿童,如果存在该综合征的其他特征,临床医生应警惕BWS的可能性。

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本文引用的文献

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Beckwith-Wiedemann syndrome.贝克威思-威德曼综合征。
Eur J Hum Genet. 2010 Jan;18(1):8-14. doi: 10.1038/ejhg.2009.106.
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Lipoma of the oral and maxillofacial region: Site and subclassification of 125 cases.口腔颌面部脂肪瘤:125例的发病部位及亚分类
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2004 Oct;98(4):441-50. doi: 10.1016/j.tripleo.2004.02.071.
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Colon polyps in Beckwith-Wiedmann syndrome: role of imprinted genes.
Gastroenterology. 2000 Mar;118(3):637. doi: 10.1016/s0016-5085(00)70277-0.

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