先天性腭瘘病例报告及文献复习

Sneha Gulati, A. Yadav, R. Sharma
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引用次数: 0

摘要

先天性腭瘘(CPF)是腭裂最罕见的表型变异,通常与黏膜下腭裂(SCP)相关。孤立性腭瘘无SCP的报道很少。我们在此报告一例4岁儿童,患有10mm × 5mm CPF,表现为鼻反流和语言异常。患者有单侧腭肌错位,无典型的SCP特征。修复使用翻转皮瓣和Bardach的两长瓣腭成形术和行内瓣成形术。愈合无任何并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Congenital palatal fistula: Case report and review of literature
Congenital palatal fistula (CPF) is the rarest phenotypic variation of cleft palate, commonly associated with submucous cleft palate (SCP). Isolated palatal fistula without SCP has been reported only rarely. We report here the case of a 4-year-old child, with a 10 mm × 5 mm CPF, presenting with nasal regurgitation and speech abnormalities. The patient had unilateral palatal muscular malposition without classical features of SCP. The repair was performed using turnover flaps and Bardach's two-long flap palatoplasty and intravelar veloplasty. Healing occurred without any complications.
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