Resnick Cory M, Estroff Judy A, Kooiman Tessa D, Calabrese Carly E, Koudstaal Maarten J, Padwa Bonnie L
Assistant Professor of Oral and Maxillofacial Surgery, Harvard School of Dental Medicine and Harvard Medical School, Boston; Oral and Maxillofacial Surgeon, Department of Plastic and Oral Surgery, Boston Children's Hospital, Boston, MA.
Associate Professor of Radiology, Harvard Medical School, Boston; Radiologist, Division Chief, Fetal-Neonatal Imaging, Department of Radiology, Advanced Fetal Care Center, Boston Children's Hospital, Boston, MA.
J Oral Maxillofac Surg. 2018 May;76(5):1058-1064. doi: 10.1016/j.joms.2017.10.006. Epub 2017 Oct 16.
The etiology of the palatal cleft in Robin sequence (RS) is unknown. The purpose of this study was to assess the position of the fetal tongue at prenatal magnetic resonance imaging (MRI) and to suggest a potential relation between tongue position and development of the cleft palate seen in most patients with RS.
This is a retrospective case-and-control study including fetuses with prenatal MRIs performed in the authors' center from 2002 to 2017. Inclusion criteria were 1) prenatal MRI of adequate quality, 2) liveborn infant, and 3) postnatal diagnosis of RS (Robin group) or cleft lip and palate (CLP group). Patients with postnatal RS without a palatal cleft were excluded. A control group with normal facial morphology was matched by gestational age. The outcome variable was tongue position at fetal MRI, described as within the cleft, along the floor of the mouth (normal), other, or indeterminate.
One hundred twenty-two patients with mean gestational age at MRI of 25.8 ± 4.9 weeks were included (Robin, n = 21 [17%]; CLP, n = 47 [39%]; control, n = 54 [44%]). The tongue was visualized within the palatal cleft in 76.2% of the Robin group and 4.3% of the CLP group. The tongue was found along the floor of the mouth (normal) in the remainder of the Robin and CLP groups and in 100% of the control group.
These findings suggest a relation between in utero tongue position and the development of cleft palate in RS.
罗宾序列征(RS)中腭裂的病因尚不清楚。本研究的目的是评估胎儿在产前磁共振成像(MRI)时舌头的位置,并提示舌头位置与大多数RS患者中所见腭裂发育之间的潜在关系。
这是一项回顾性病例对照研究,纳入了2002年至2017年在作者所在中心进行产前MRI检查的胎儿。纳入标准为:1)质量合格的产前MRI;2)活产婴儿;3)产后诊断为RS(罗宾组)或唇腭裂(CLP组)。排除产后有RS但无腭裂的患者。根据孕周匹配面部形态正常的对照组。观察变量为胎儿MRI时的舌头位置,分为在腭裂内、沿口腔底部(正常)、其他或不确定。
共纳入122例患者,MRI时的平均孕周为25.8±4.9周(罗宾组,n = 21 [17%];CLP组,n = 47 [39%];对照组,n = 54 [44%])。罗宾组76.2%的患者舌头位于腭裂内,CLP组为4.3%。罗宾组和CLP组其余患者以及100%的对照组患者舌头沿口腔底部(正常)。
这些发现提示宫内舌头位置与RS中腭裂的发育之间存在关联。