Kado Isamu, Ogashira Shintaro, Ono Shigehiro, Koizumi Koichi, Nakagawa Takayuki, Yoshimi Yuki, Kunimatsu Ryo, Ito Shota, Koizumi Yuma, Ogasawara Tomohiro, Aikawa Tomonao, Tanimoto Kotaro
Department of Orthodontics and Craniofacial Developmental Biology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, JPN.
Department of Oral and Maxillofacial Surgery, Hiromashi University Hospital, Hiroshima, JPN.
Cureus. 2024 May 9;16(5):e59964. doi: 10.7759/cureus.59964. eCollection 2024 May.
Sturge-Weber syndrome (SWS) is characterized by hemangiomas, glaucoma, and central nervous system disorders. Here, we report the case of a 15-year-old boy with SWS and upper-lip hypertrophy who underwent surgical orthodontic treatment for correction of a large overjet and deep overbite. In addition to the a large overjet and deep overbite, interdental spacing was observed in both the arches. The mandible was retrognathic and deviated to the right side. No maxillary occlusal canting or temporomandibular joint symptoms were observed. The patient was diagnosed with skeletal maxillary protrusion with spaced dentition and mandibular deviation to the right due to SWS. After presurgical orthodontic treatment using a multibracket appliance, we performed a sagittal split ramus osteotomy (SSRO) alone due to the presence of a hemangioma around the maxilla. No abnormal bleeding or cerebral hemorrhage due to increased blood pressure was observed during the SSRO. Postoperatively, the maxillary and mandibular arches were well-aligned, the deep overbite and excessive overjet improved, and bilateral angle class I molar and canine relationships were established. Furthermore, mandibular deviation improved, and the midlines of both arches approximately coincided with the facial midline. In conclusion, orthognathic surgery is feasible in patients with SWS after carefully evaluating the sites and sizes of the hemangiomas.
斯特奇-韦伯综合征(SWS)的特征为血管瘤、青光眼和中枢神经系统疾病。在此,我们报告一例15岁患有SWS且上唇肥大的男孩,其接受了外科正畸治疗以矫正严重的覆盖和深覆合。除严重覆盖和深覆合外,在上下牙弓均观察到牙间隙。下颌后缩且向右侧偏斜。未观察到上颌咬合倾斜或颞下颌关节症状。该患者被诊断为因SWS导致的骨骼性上颌前突伴牙列间隙及下颌向右侧偏斜。在使用多托槽矫治器进行术前正畸治疗后,由于上颌周围存在血管瘤,我们仅进行了矢状劈开下颌升支截骨术(SSRO)。在SSRO过程中未观察到因血压升高导致的异常出血或脑出血。术后,上颌和下颌牙弓排列良好,深覆合和严重覆盖得到改善,双侧安氏I类磨牙和尖牙关系得以建立。此外,下颌偏斜得到改善,上下牙弓中线大致与面部中线重合。总之,在仔细评估血管瘤的部位和大小后,正颌手术对于SWS患者是可行的。