Guimaraes Carolina V A, Donnelly Lane F, Shott Sally R, Amin Raouf S, Kalra Maninder
Department of Radiology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Ave., MLC 5031, Cincinnati, OH 45229-3039, USA.
Pediatr Radiol. 2008 Oct;38(10):1062-7. doi: 10.1007/s00247-008-0941-7. Epub 2008 Aug 7.
Children with Down syndrome are described as having macroglossia as well as midface hypoplasia. We reviewed anatomic parameters on MRI to determine whether adolescents with Down syndrome have true macroglossia or relatively large tongues compared to the small size of their oral cavity. This has implications for the treatment of obstructive sleep apnea, which occurs at a relatively high rate among patients with Down syndrome.
To determine whether adolescents with Down syndrome have relative rather than true macroglossia.
On sagittal and axial MR images, parameters for tongue size (area in sagittal midline), the bony craniofacial confines of the retroglossal pharynx (distance between the mandibular rami and distance between the posterior aspect of the mental mandible and the anterior aspect of the spine), and the size of the tongue relative to the craniofacial bony parameters [tongue area/(transverse diameter x anterior-to-posterior diameter)] were compared between 16 patients with Down syndrome and 16 age- and gender-matched controls.
The tongue area was significantly smaller in patients with Down syndrome (2,432 mm2) than in the control patients (2,767 mm2; P=0.02). The craniofacial bony parameters were also smaller in patients with Down syndrome than in the controls (left-right 69.8 vs. 80.1 mm, P<0.001; anterior-posterior 64.2 vs. 74.9 mm, P<0.001). However, the size of the tongue relative to the craniofacial parameters was larger in the patients with Down syndrome (0.54) than in the controls (0.46; P<0.001).
Children with Down syndrome do not have true macroglossia but have relatively large tongues compared to the bony confines of the oral cavity.
唐氏综合征患儿被描述为有巨舌症以及面中部发育不全。我们回顾了MRI上的解剖学参数,以确定唐氏综合征青少年是真正的巨舌症,还是相较于其口腔较小的尺寸而言舌头相对较大。这对阻塞性睡眠呼吸暂停的治疗有影响,阻塞性睡眠呼吸暂停在唐氏综合征患者中发生率相对较高。
确定唐氏综合征青少年是否有相对而非真正的巨舌症。
在矢状面和轴位MR图像上,比较了16例唐氏综合征患者和16例年龄及性别匹配的对照组患者的舌大小参数(矢状中线面积)、舌后咽的颅骨面部边界(下颌支之间的距离以及颏下颌骨后缘与脊柱前缘之间的距离),以及舌头大小相对于颅面骨参数的大小[舌面积/(横径×前后径)]。
唐氏综合征患者的舌面积(2432平方毫米)显著小于对照组患者(2767平方毫米;P = 0.02)。唐氏综合征患者的颅面骨参数也小于对照组(左右径69.8对80.1毫米,P < 0.001;前后径64.2对74.9毫米,P < 0.001)。然而,唐氏综合征患者舌头大小相对于颅面参数的值(0.54)大于对照组(0.46;P < 0.001)。
唐氏综合征患儿没有真正的巨舌症,但相较于口腔的骨边界而言,他们的舌头相对较大。