Boutros Sean, Shetye Pradip R, Ghali Shadi, Carter Christina R, McCarthy Joseph G, Grayson Barry H
Hermann Hospital and Hermann Children's Hospital Houston, Houston, Texas, USA.
J Craniofac Surg. 2007 Jan;18(1):146-50. doi: 10.1097/01.scs.0000248655.53405.a7.
The purpose of this study was to examine mandibular morphology and growth in patients with Crouzon, Pfeiffer, and Apert syndromes using posteroanterior cephalograms. Fifteen patients with Apert (n = 2), Crouzon (n = 11), and Pfeiffer (n = 2) (11 female, 4 male) syndrome were included in this study. All patients had serial posteroanterior cephalograms at 5, 10, and 15 years of age. The bicondylar width, bigonial width, bicondylar/bigonial ratio, and ramus to intercondylar plane angle for each patient were measured on the cephalograms and compared with age-match controls. An analysis of variance analysis was carried out to detect differences between patients and controls and sex differences between patients. In both male and female patients, there was a statistically significant reduction in bicondylar width compared with age-matched controls. Male patients also had a statistically significant increase in bigonial width compared with controls and female patients at 10 and 15 years. The resulting bicondylar/bigonial ratios were significantly reduced, and the ramus to intercondylar plane angles were significantly increased in both male and female patients compared with controls. Unlike previous reports of patients with syndromic synostosis, this study demonstrates that the mandible has significant morphologic and growth abnormalities, including constriction of bicondylar width with near normal bigonial width in female patients. These findings suggest a narrowing at the cranial base with resulting restriction of normal transverse mandibular growth at the condyle. The secondary nature of the mandibular finding is suggested by the near normal or increased transverse growth at the gonion in females and males, respectively. Consequently, the ramus appears torqued inward, forming a greater angle with the cranial base.
本研究的目的是使用后前位头影测量片检查患有克鲁宗综合征、菲佛综合征和阿佩尔综合征患者的下颌骨形态和生长情况。本研究纳入了15例患有阿佩尔综合征(n = 2)、克鲁宗综合征(n = 11)和菲佛综合征(n = 2)的患者(11名女性,4名男性)。所有患者在5岁、10岁和15岁时均拍摄了系列后前位头影测量片。在头影测量片上测量每位患者的双侧髁突宽度、下颌角间宽度、双侧髁突/下颌角间宽度比值以及升支与髁间平面夹角,并与年龄匹配的对照组进行比较。进行方差分析以检测患者与对照组之间的差异以及患者之间的性别差异。在男性和女性患者中,与年龄匹配的对照组相比,双侧髁突宽度均有统计学意义的减小。男性患者在10岁和15岁时,与对照组和女性患者相比,下颌角间宽度也有统计学意义的增加。与对照组相比,男性和女性患者的双侧髁突/下颌角间宽度比值均显著降低,升支与髁间平面夹角均显著增加。与先前关于综合征性颅缝早闭患者的报道不同,本研究表明下颌骨存在显著的形态和生长异常,包括女性患者双侧髁突宽度变窄而下颌角间宽度接近正常。这些发现提示颅底变窄,导致髁突处下颌骨正常横向生长受限。下颌骨 findings 的继发性性质分别由女性和男性下颌角处接近正常或增加的横向生长所提示。因此,升支似乎向内扭转,与颅底形成更大的角度。