Constantinides C G, Cywes S
S Afr Med J. 1983 Aug 20;64(8):293-4.
A rare case of complete median mandibular cleft without associated anomalies of the adjacent soft-tissue structures is presented. Aplasia of the epiglottis was also present, a combination not previously reported. The anomaly seems to be the result of arrested development of the lower half of the first branchial arch, and in particular of the mesenchymal elements. It may assume varying degrees of severity, ranging from an incomplete cleft of the lower lip or mandible (or both) to a complete midline cleft of the lower lip, mandible and tongue, sometimes with associated deformities of soft-tissue structures derived from the lower branchial arches in the neck. Although there is no consensus on the timing of corrective procedures, the strategy favoured by most seems to be early repair of the soft-tissue abnormalities and deferment of the mandibular repair until after puberty. Persistent aspiration due to the absence of the epiglottis necessitated performance of a tracheostomy and feeding gastrostomy in our patient. The patient sustained an anoxic episode as a result of tracheostomy obstruction and died a few weeks later.
本文报告一例罕见的下颌正中完全性腭裂,且相邻软组织结构无相关异常。同时还存在会厌发育不全,此前未见这种组合情况的报道。该异常似乎是第一鳃弓下半部,尤其是间充质成分发育停滞的结果。其严重程度可能不同,从下唇或下颌骨(或两者)的不完全腭裂到下唇、下颌骨和舌的完全中线腭裂,有时还伴有颈部下鳃弓衍生的软组织结构的相关畸形。尽管对于矫正手术的时机尚无共识,但大多数人倾向的策略似乎是早期修复软组织异常,将下颌修复推迟到青春期后。由于会厌缺失导致持续误吸,我们的患者需要进行气管切开术和胃造口术喂养。患者因气管切开术阻塞发生缺氧事件,几周后死亡。