Ahmed Mamdouh, Ali Sherif
Oral and Maxillofacial Surgery Department, Faculty of Dentistry, Cairo University, Cairo, Egypt; Cranio-maxillofacial surgery Department, Nasser institute for research and treatment, Cairo, Egypt.
Oral and Maxillofacial Surgery Department, Faculty of Dentistry, Cairo University, Cairo, Egypt.
Int J Surg Case Rep. 2019;57:52-56. doi: 10.1016/j.ijscr.2019.03.005. Epub 2019 Mar 16.
INTRODUCTION, Hemifacial microsomia is the second most common craniofacial congenital anomaly. It corresponds to a group of malformations ranging from minimal facial asymmetry to sever form affecting mandible, soft tissues, orbit, ear, and cranial nerves. PRESENTATION OF CASE, We present a case of 6 years old patient with Kaban class III hemifacial microsomia with anotia. Temporomandibular joint was reconstructed by costochondral graft using computer guided surgery (simulation and rapid prototyping). A computer guided soft tissue guide, mandibular, and maxillomandibular/zygomatic models were constructed using rapid prototyping technology. The customized computer guided soft tissue guide was used to localize the proper position of skin incision, the mandibular model was used for preoperative reconstruction plate bending, and the maxillomandibular/zygomatic model was used to estimate the rib graft length and position. Postoperative assessment showed proper positioning of the graft, with no complications or facial nerve affection. DISCUSSION, In this report, we introduce a new computer guided technique to estimate and identify the proper position of the temporomandibular joint graft based on patient CT. This technique eliminated the need of extended incisions with excessive dissection and provided a more accessible field for rib graft fixation, facilitating the surgical procedures. CONCLUSION, The use of computer guided surgery (simulation and rapid prototyping) for temporomandibular joint reconstruction in Kaban III hemifacial microsomia with anotia facilitates the surgical procedure, minimizes procedure time, increases precision, and reduces possible complications.
引言,半侧颜面短小畸形是第二常见的颅面先天性异常。它对应于一组从轻微面部不对称到严重畸形的情况,严重畸形会影响下颌骨、软组织、眼眶、耳朵和颅神经。病例介绍,我们报告一例6岁患有卡班III级半侧颜面短小畸形并伴有无耳畸形的患者。采用计算机辅助手术(模拟和快速成型)通过肋软骨移植重建颞下颌关节。利用快速成型技术构建了计算机辅助软组织导板、下颌骨模型以及上颌下颌/颧骨模型。定制的计算机辅助软组织导板用于确定皮肤切口的正确位置,下颌骨模型用于术前重建钢板的弯曲,上颌下颌/颧骨模型用于估计肋骨移植的长度和位置。术后评估显示移植部位定位正确,无并发症且未累及面神经。讨论,在本报告中,我们介绍了一种基于患者CT来估计和确定颞下颌关节移植正确位置的新型计算机辅助技术。该技术无需进行广泛的切口和过度的解剖,为肋骨移植固定提供了更易操作的视野,简化了手术过程。结论,对于患有无耳畸形的卡班III级半侧颜面短小畸形患者,使用计算机辅助手术(模拟和快速成型)进行颞下颌关节重建可简化手术过程,缩短手术时间,提高精度,并减少可能的并发症。