鼻窝畸形与旁脉面裂:新观点。

E N Garabedian, V Ducroz, G Roger, F Denoyelle, M Catala
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引用次数: 0

摘要

后肛门闭锁可能与其他颅面畸形有关,包括不同程度的鼻窝畸形,并且可能是旁位面裂的一部分(如Tessier等人[1977]所描述的)。我们发现了5例与Tessier氏旁膈面裂相对应的综合临床因素,包括眼睑缺损、轻度至重度后鼻窝和鼻窝异常、筛发育不全和前颅底畸形,有时伴有侧鼻和半鼻发育不全。这些观察促使我们,首先,阐述一个概念,解释可能涉及的胚胎学机制;第二,提出一种基于解剖学和病原胚胎学考虑的新分类;最后,建议使用经鼻入路来恢复后肛门的渗透性,因为在这种情况下鼻内激光治疗是特别危险的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nasal fossa malformations and paramedian facial cleft: new perspectives.

Choanal atresia may be associated with other cranio-facial malformations, including various degrees of nasal fossa malformation, and may be a part of paramedian facial clefts (as described by Tessier et al. [1977]). We identified five such cases with combined clinical elements corresponding to Tessier's paramedian facial cleft, including eyelid coloboma, mild to severe choanal and nasal fossa anomalies, ethmoidal hypoplasia and anterior skull base malformation, sometimes with proboscis lateralis and half-nose hypoplasia. These observations incited us, first, to elaborate a conception which accounts for the likely embryological mechanisms involved; second, to propose a new classification based on anatomical and pathogenic embryological considerations; and last, to propose the use of transpalatal approach to restore choanal permeability, since endonasal laser therapy is particularly dangerous in such cases.

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