Bolan Michele, Ferreira Meire Coelho, Almeida Izabel Cristina Santos, D'Agostini Derech Carla, Ribeiro Gerson Luiz Ulema
Federal University of Santa Catarina, Florianópolis, Brazil.
Am J Orthod Dentofacial Orthop. 2005 Sep;128(3):385-7. doi: 10.1016/j.ajodo.2005.02.002.
A girl (aged 8.5 years) with Klippel-Trénaunay-Weber syndrome received orthodontic treatment that included rapid palatal expansion. The patient had early and complete intraoral dental eruption with a posterior crossbite and an expressive transverse atresic maxilla. No carious lesions were found, but hemangioma-like changes of the mucosa were observed. A Haas palatal expander was activated for 15 days and remained in the oral cavity for splinting purposes for 6 months; it was then replaced by a removable acrylic plate with a Hawley arch. Klippel-Trénaunay-Weber syndrome did not impede rapid maxillary expansion, and the treatment was successful.
一名患有克-特-韦综合征（Klippel-Trénaunay-Weber syndrome）的8.5岁女孩接受了正畸治疗，其中包括快速腭扩展。该患者牙齿早期完全萌出于口腔内，存在后牙反合以及上颌骨横向发育不全。未发现龋损，但观察到黏膜有血管瘤样改变。使用哈斯腭扩展器激活15天，并在口腔内保留6个月用于夹板固定；之后被带有霍利弓的可摘丙烯酸板取代。克-特-韦综合征并未妨碍上颌快速扩展，治疗取得成功。
