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下唇和下颌正中裂:病例报告、新的胚胎学假说及分类

Median cleft of the lower lip and mandible: case reports, a new embryologic hypothesis, and subdivision.

作者信息

Oostrom C A, Vermeij-Keers C, Gilbert P M, van der Meulen J C

机构信息

Department of Plastic and Reconstructive Surgery, University Hospital, Sophia/Dijkzigt, Rotterdam, The Netherlands.

出版信息

Plast Reconstr Surg. 1996 Feb;97(2):313-20. doi: 10.1097/00006534-199602000-00006.

Abstract

Median clefts of the lower lip and mandible are rare. In the literature so far, about 62 cases have been described. In addition, three more patients are presented here. These cases show a broad variation in the severity of this deformity, ranging from a simple notch in the vermillion to a complete cleft of the lip involving the tongue, the chin, the mandible, the supporting structures of the median of the neck, and the manubrium sterni. Several hypotheses concerning the pathogenesis of median clefts of the lip and mandible have been proposed. Most authors consider it to be a failure of fusion of the first pair of branchial arches or failure of mesodermal penetration into the midline. From our embryologic point of view, however, instead of paired branchial arches, only one first branchial arch develops during the early embryonic period (< or = 17 mm crown-rump length). Within this first branchial arch, two mandibular processes grow out, separated by a groove in the median. These mandibular processes do not fuse but merge during the late embryonic period (> or = 17 mm to < or = 60 mm crown-rump length). In the same developmental period, there is formation of the lip and the alveolar process and the anlage and outgrowth of one membrane bone center in each mandibular process, resulting in the formation of the mandible with its symphysis. As a consequence of the preceding, we propose the following subdivision of the median clefts of the lip and/or mandible: Hypoplasia of the mandibular processes during the early embryonic period will lead to the severest cleft of the mandible extending into the neck. During the late embryonic period, the less severe median clefts will develop. Disturbances of the outgrowth of bone centers of the mandible, resulting in nonformation of its symphysis, cause clefting of the mandible with involvement of all related soft tissues. Defects in the merging process produce just a notch of the vermilion or a higher cleft of the lower lip with or without involvement of the alveolar process of the mandible. In conclusion, the variety of the clefts in the median of the lower lip and/or mandible as well as the low rate of incidence can be explained by the embryologic hypothesis proposed here.

摘要

下唇和下颌正中裂较为罕见。在目前的文献中,已描述了约62例。此外,本文还报告了另外3例患者。这些病例显示出这种畸形严重程度的广泛差异,从唇红部的简单切迹到累及舌、颏部、下颌骨、颈部正中支持结构和胸骨柄的完全唇裂。关于唇和下颌正中裂的发病机制,已经提出了几种假说。大多数作者认为这是第一对鳃弓融合失败或中胚层向中线穿透失败所致。然而,从我们的胚胎学观点来看,在胚胎早期(头臀长≤17mm),只发育一个第一鳃弓,而不是成对的鳃弓。在这个第一鳃弓内,两个下颌突长出,中间由一条中线沟隔开。这些下颌突在胚胎后期(头臀长>17mm至≤60mm)并不融合而是合并。在同一发育时期,形成了唇和牙槽突,每个下颌突中有一个膜性骨中心的原基和生长,导致下颌骨及其联合的形成。基于上述情况,我们提出唇和/或下颌正中裂的如下分类:胚胎早期下颌突发育不全将导致最严重的下颌裂并延伸至颈部。在胚胎后期,将出现较轻的正中裂。下颌骨骨中心生长紊乱,导致联合未形成,引起下颌裂并累及所有相关软组织。合并过程中的缺陷仅产生唇红切迹或下唇较高的裂,可伴有或不伴有下颌牙槽突受累。总之,下唇和/或下颌正中裂的多样性以及低发病率可以用本文提出的胚胎学假说解释。

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