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腭裂软腭脂肪瘤:一例罕见先天性异常的病例报告

Lipoma of the cleft soft palate: a case report of a rare congenital anomaly.

作者信息

Mahabir R C, Mohammad J A, Courtemanche D J

机构信息

University of British Columbia, Vancouver, Canada.

出版信息

Cleft Palate Craniofac J. 2000 Sep;37(5):503-5. doi: 10.1597/1545-1569_2000_037_0503_lotcsp_2.0.co_2.

DOI:10.1597/1545-1569_2000_037_0503_lotcsp_2.0.co_2
PMID:11034034
Abstract

Congenital tumors of the oral cavity are extremely uncommon. The teratoid tumors (epiganthi, dermoid, and hairy polyps) account for almost all of the reported cases and are not infrequently associated with cleft of the soft palate. Of the remaining tumors in the pediatric cleft palate population, infantile lipoma of the oral cavity is exceedingly rare. A case of a congenital lipoma associated with a cleft of the soft palate is presented. The review of the literature, the description of the lesion, the diagnosis, and the management of this finding are outlined.

摘要

口腔先天性肿瘤极为罕见。畸胎样肿瘤(先天性皮样囊肿、皮样囊肿和毛发息肉)几乎占所有报告病例,且常与软腭裂相关。在小儿腭裂人群中的其余肿瘤中,口腔婴儿脂肪瘤极为罕见。本文报告一例与软腭裂相关的先天性脂肪瘤病例。概述了文献回顾、病变描述、诊断及该病例的处理。

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引用本文的文献

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Intraoral Lipoma: A Case Report.口腔内脂肪瘤:一例报告。
J Pharm Bioallied Sci. 2023 Jul;15(Suppl 2):S1338-S1340. doi: 10.4103/jpbs.jpbs_143_23. Epub 2023 Apr 28.
2
Congenital hairy polyp associated with cleft palate-a rare entity.先天性毛发状息肉伴腭裂——一种罕见的病症。
Int J Clin Pediatr Dent. 2009 Jan;2(1):46-8. doi: 10.5005/jp-journals-10005-1042. Epub 2009 Apr 26.