Cerrati Eric W, Ahmed Omar H, Rickert Scott M
Department of Otolaryngology-Head and Neck Surgery, New York University School of Medicine, New York, NY, USA.
Department of Otolaryngology-Head and Neck Surgery, New York University School of Medicine, New York, NY, USA.
Am J Otolaryngol. 2015 Sep-Oct;36(5):707-9. doi: 10.1016/j.amjoto.2015.04.008. Epub 2015 Apr 16.
Congenital maxillomandibular syngnathia, or fusion of the jaws, is a rare condition that has a broad spectrum of presentations. The restricted mouth opening can lead to issues with feeding, swallowing, and respiration resulting in failure to thrive and temporomandibular joint ankylosis. Early recognition and treatment is necessary for proper growth and development.
We report a 1-day-old male with isolated bilateral soft tissue alveolar fibrous bands. He presented with difficulty feeding secondary to trismus. No bony or muscular involvement in the synechiae was noted and the remainder of the physical exam was unremarkable. The bilateral alveolar synechiae were divided under local anesthesia using surgical scissors. The patient immediately showed improvement in mouth opening and had resolution of his feeding problems. He is now gaining weight and developing appropriately.
The accompanying review of the literature demonstrates only 11 cases worldwide of isolated maxillomandibular fusion. Depending upon the composition of the synechiae, simple surgical division under local anesthesia can be curative.
先天性上颌下颌融合,即颌骨融合,是一种罕见的病症,临床表现多样。张口受限会导致喂养、吞咽和呼吸问题,进而导致发育不良和颞下颌关节强直。早期识别和治疗对于正常生长发育至关重要。
我们报告一例1日龄男性患儿,患有孤立性双侧软组织牙槽纤维带。他因牙关紧闭出现喂养困难。未发现粘连中有骨或肌肉受累,其余体格检查无异常。在局部麻醉下用手术剪分离双侧牙槽粘连。患儿张口立即改善,喂养问题得到解决。他现在体重增加,发育正常。
文献回顾显示,全球仅有11例孤立性上颌下颌融合病例。根据粘连的构成,局部麻醉下简单的手术分离即可治愈。