Doucet Jean-Charles, Morrison Archie D
Oral and Maxillofacial Surgery, Dalhousie University, Halifax, Nova Scotia, Canada.
Craniomaxillofac Trauma Reconstr. 2011 Mar;4(1):11-8. doi: 10.1055/s-0031-1272904.
Systemic sclerosis (SSc) is a multisystem connective tissue disease of unknown etiology. The hallmark of SSc is scleroderma, referring to the presence of thickened, hardened skin. Oral and maxillofacial manifestations of the disease are numerous including masklike appearance, trismus, muscular atrophy, thin atrophied lips, secondary microstomia, xerostomia, rigidity of tongue and lips, widening of the periodontal ligament space, trigeminal neuralgia, and resorption of the mandible. A 35-year-old woman with limited cutaneous SSc presented with bilateral mandibular condylysis, severe class II mandibular deficiency, and large anterior open bite and limited range of mandibular opening at 27 mm. Surgical correction consisted of bilateral total temporomandibular joint reconstruction with stock prostheses combined with Le Fort I maxillary impaction and functional advancement genioplasty. This resulted in a functional occlusion with elimination of her open bite and a more esthetic profile. Her occlusion has remained stable at 7 months. The incidence of mandibular resorption in SSc has been found to be 20% to 33%. The mandibular angles are most commonly involved (37.6%), followed by the condyle (20.8%), coronoid process (20.0%), and the posterior border of the ascending ramus (14.4%). Bilateral condylysis is present in 13.7% of the cases. Very few cases of surgical correction of malocclusion induced by SSc-related condylysis have been reported in the literature. To the best of our knowledge, this is the first case report of bilateral condylysis from SSc where surgical replacement of the resorbed condyles was attempted. Bilateral total temporomandibular joint replacement can give these patients a functional occlusion, improved facial balance, and improved quality of life.
系统性硬化症(SSc)是一种病因不明的多系统结缔组织疾病。SSc的标志是硬皮病,指皮肤增厚、变硬。该疾病的口腔颌面部表现众多,包括面具样面容、牙关紧闭、肌肉萎缩、嘴唇变薄萎缩、继发性小口畸形、口干、舌和嘴唇僵硬、牙周膜间隙增宽、三叉神经痛以及下颌骨吸收。一名35岁的局限性皮肤型SSc女性患者出现双侧下颌髁突溶解、严重的II类下颌骨发育不全、严重的前牙开合以及下颌开口度受限,仅为27毫米。手术矫正包括使用库存假体进行双侧全颞下颌关节重建,联合Le Fort I型上颌骨截骨术和功能性前移颏成形术。这实现了功能性咬合,消除了她的前牙开合,面部轮廓更美观。术后7个月,她的咬合一直保持稳定。SSc患者下颌骨吸收的发生率为20%至33%。下颌角最常受累(37.6%),其次是髁突(20.8%)、冠突(20.0%)和升支后缘(14.4%)。13.7%的病例存在双侧髁突溶解。文献中报道的由SSc相关髁突溶解引起的错牙合畸形手术矫正病例极少。据我们所知,这是首例尝试对SSc导致的双侧髁突溶解进行手术置换吸收髁突的病例报告。双侧全颞下颌关节置换可为这些患者提供功能性咬合、改善面部平衡并提高生活质量。