Ramly Elie P, Yu Jason W, Eisemann Bradley S, Yue Olivia, Alfonso Allyson R, Kantar Rami S, Staffenberg David A, Shetye Pradip R, Flores Roberto L
Hansjörg Wyss Department of Plastic Surgery, NYU Langone Health, New York, NY.
J Craniofac Surg. 2020 Jul-Aug;31(5):1343-1347. doi: 10.1097/SCS.0000000000006328.
The authors present an institutional experience treating congenital and acquired temporomandibular joint (TMJ) ankylosis, detailing outcomes and potential risk factors of recurrence.
Retrospective chart review identified patients with TMJ ankylosis (1976-2019). Clinical records, operative reports, and imaging studies were reviewed for demographics, surgical operations, and ankylosis including maximal interincisal opening (MIO) and re-ankylosis.
Forty-four TMJs with bony ankylosis were identified in 28 patients (mean age at any initial mandibular surgery: 3.7; range:0-14 years). Follow-up was 13.7 ± 5.9 years. Sixteen (57.1%) patients had bilateral ankylosis; 27(96.4%) had syndromes. Nine patients had congenital ankylosis, 16 had iatrogenic ankylosis (4.5 ± 3.7 years from initial distraction osteogenesis or autologous mandibular reconstruction) referred from outside institutions in 6 instances, and 3 had post-infectious ankylosis. Patients having their first mandibular operation at a younger age had more frequent reoperations for recurrent TMJ ankylosis, although this did not reach statistical significance. Mean improvement in MIO was 21.4 ± 7.3 mm. Ankylosis recurred in 21 (75%) patients. Five patients with congenital TMJ ankylosis required gastrostomy and remained at least partially dependent. Five patients had tracheostomy at the time of TMJ ankylosis surgery: 2 were eventually decannulated and 3 required repeat tracheostomy after ankylosis recurrence and remained tracheostomy-dependent.
The clinical course of TMJ ankylosis in children affected by craniofacial differences is complex and typically involves a high rate of recurrence and multiple reoperations despite initial improvement in postoperative MIO. Younger age at initial mandibular surgery and number of operations require further investigation as potential predictors of recurrent TMJ ankylosis as well as tracheostomy and gastrostomy dependence.
作者介绍了治疗先天性和后天性颞下颌关节(TMJ)强直的机构经验,详细阐述了治疗结果及复发的潜在危险因素。
通过回顾性病历审查确定患有TMJ强直的患者(1976 - 2019年)。对临床记录、手术报告和影像学研究进行审查,以获取人口统计学信息、手术操作以及强直情况,包括最大切牙间开口度(MIO)和再强直情况。
在28例患者中确定了44个患有骨性强直的TMJ(初次下颌手术时的平均年龄:3.7岁;范围:0 - 14岁)。随访时间为13.7 ± 5.9年。16例(57.1%)患者为双侧强直;27例(96.4%)患有综合征。9例患者为先天性强直,16例为医源性强直(距初次牵张成骨或自体下颌骨重建4.5 ± 3.7年),其中6例由外部机构转诊,3例为感染后强直。初次下颌手术时年龄较小的患者因复发性TMJ强直进行再次手术的频率更高,尽管这未达到统计学意义。MIO的平均改善为21.4 ± 7.3毫米。21例(75%)患者出现强直复发。5例先天性TMJ强直患者需要胃造口术,且至少部分依赖他人照顾。5例患者在TMJ强直手术时进行了气管切开术:2例最终拔管,3例在强直复发后需要再次气管切开术,且一直依赖气管切开。
受颅面差异影响的儿童TMJ强直的临床病程复杂,尽管术后MIO最初有所改善,但通常复发率高且需要多次再次手术。初次下颌手术时年龄较小以及手术次数作为复发性TMJ强直以及气管切开术和胃造口术依赖的潜在预测因素需要进一步研究。