Ysunza Antonio, Carmen Pamplona Maria, Santiago Morales M A
Cleft Palate Clinic, Hospital Gea Gonzalez, Mexico City, Mexico.
Int J Pediatr Otorhinolaryngol. 2011 Oct;75(10):1255-9. doi: 10.1016/j.ijporl.2011.07.001. Epub 2011 Aug 4.
Velocardiofacial syndrome (VCFS) is the most common genetic syndrome associated with cleft palate. There are reports describing several anomalies associated with the palatal cleft in patients with VCFS, which can affect the characteristics of the velopharyngeal insufficiency (VPI) in these cases.
The purpose of this study is to assess velopharyngeal sphincter function during speech, using videonasopharyngoscopy (VNP) and videofluoroscopy (VF), in patients with VCFS, as compared with patients with non-syndromic palatal clefts (NSCP).
Twenty patients with VCFS corroborated by a FISH test were studied. All patients showed a palatal cleft. All patients had received previous management including speech therapy and palatal repair. These patients underwent a thorough clinical speech evaluation, including VNP and VF. Twenty patients with NSCP matched by sex, type of cleft and within the age range of the patients with VCFS were studied as controls.
From the patients with VCFS, seventeen patients showed a submucous cleft palate. Three patients showed sub-total cleft of the secondary palate. Fourteen patients (70%) showed a coronal velopharyngeal closure pattern. Six patients (30%) showed a circular pattern. In contrast, 10 patients (50%) from the NSCP group showed a circular pattern, two of them showed a Passavant's ridge. Seven patients (35%) showed a coronal pattern and 3 patients (15%) showed a saggital pattern. Mean velum (V) and lateral pharyngeal wall (LPW) motion were significantly decreased in patients with VCFS (V=46% vs 71%; LPW=14% vs 30%; P<0.001). Size of the defect during speech was significantly increased in patients with VCFS (34.57% vs 67.37%; P<0.001).
Velopharyngeal valving during speech is significantly different in patients with VCFS as compared with patients with NSCP. Several anomalies associated with the palatal cleft in patients with VCFS can explain these differences. Thus, the surgical approach for repairing a palatal cleft should consider these differences. Moreover, surgical planning should be performed according to the specific findings of the velopharyngeal sphincter in order to improve speech outcome.
腭心面综合征(VCFS)是与腭裂相关的最常见的遗传综合征。有报道描述了VCFS患者中与腭裂相关的几种异常情况,这些异常情况可能会影响这些病例中的腭咽闭合不全(VPI)特征。
本研究的目的是使用鼻咽喉镜检查(VNP)和荧光透视检查(VF)评估VCFS患者与非综合征性腭裂(NSCP)患者在言语过程中的腭咽括约肌功能。
对20例经荧光原位杂交(FISH)检测证实患有VCFS的患者进行了研究。所有患者均表现为腭裂。所有患者之前都接受过包括言语治疗和腭裂修复在内的治疗。这些患者接受了全面的临床言语评估,包括VNP和VF。选取20例年龄与VCFS患者匹配、性别和腭裂类型相同的NSCP患者作为对照进行研究。
在VCFS患者中,17例表现为黏膜下腭裂。3例表现为继发腭次全裂。14例(70%)表现为冠状腭咽闭合模式。6例(30%)表现为环状模式。相比之下,NSCP组中有10例(50%)表现为环状模式,其中2例有咽后壁隆起。7例(35%)表现为冠状模式,3例(15%)表现为矢状模式。VCFS患者的软腭(V)和咽侧壁(LPW)平均运动明显减少(V = 46%对71%;LPW = 14%对30%;P < 0.001)。VCFS患者在言语过程中缺损大小明显增加(34.57%对67.37%;P < 0.001)。
与NSCP患者相比,VCFS患者在言语过程中的腭咽瓣功能有显著差异。VCFS患者中与腭裂相关的几种异常情况可以解释这些差异。因此,腭裂修复的手术方法应考虑这些差异。此外,手术规划应根据腭咽括约肌的具体检查结果进行,以改善言语效果。