Resnick Cory M, Kooiman Tessa D, Calabrese Carly E, Didier Ryne, Padwa Bonnie L, Estroff Judy A, Koudstaal Maarten J
1 Harvard School of Dental Medicine, Harvard Medical School, Boston, MA, USA.
2 Department of Plastic and Oral Surgery, Boston Children's Hospital, Boston, MA, USA.
Cleft Palate Craniofac J. 2018 Apr;55(4):562-567. doi: 10.1177/1055665617746795. Epub 2017 Dec 19.
Glossoptosis causes airway obstruction in patients with Robin sequence (RS), but little is known about the in-utero tongue. The purpose of this study was to assess shape and position of the fetal tongue on prenatal magnetic resonance imaging (MRI) to determine if this is predictive of postnatal RS.
Retrospective case-control study including fetuses with prenatal MRIs performed from 2002 to 2017. Inclusion criteria were (1) prenatal MRI of adequate quality, (2) live born and evaluated postnatally for craniofacial findings. Subjects were divided into groups based on postnatal findings: (1) RS, (2) micrognathia without RS, and (3) a gestational-age-matched control group with normal craniofacial morphology. Outcome variables were based on the prenatal MRI and included fetal tongue height, length, and width, tongue shape index (TSI, ratio of height to length), and observation of tongue touching the posterior pharyngeal wall.
A total of 116 subjects with mean gestational age at MRI of 25.6 ± 5.1 weeks were included: RS, n = 27 (23%); micrognathia, n = 35 (30%); control, n = 54 (47%). Tongue length was significantly shorter ( P = .009) and TSI was significantly larger in the RS group ( P < .0001). The tongue touched the posterior pharyngeal wall in 5 (19%) of the RS group and in no subjects in the other groups ( P < .0001).
In utero tongue shape and position were significantly different in fetuses with postnatal RS compared to those with isolated micrognathia and controls. Prenatal MRI tongue characteristics may be predictors for postnatal RS.
小颌畸形导致罗宾序列征(RS)患者气道阻塞,但对于子宫内舌的情况知之甚少。本研究的目的是在产前磁共振成像(MRI)上评估胎儿舌的形状和位置,以确定这是否可预测出生后的RS。
回顾性病例对照研究,纳入2002年至2017年进行产前MRI检查的胎儿。纳入标准为:(1)质量合格的产前MRI;(2)活产且出生后接受颅面检查评估。根据出生后检查结果将受试者分为几组:(1)RS组;(2)无RS的小颌畸形组;(3)颅面形态正常的孕周匹配对照组。观察指标基于产前MRI,包括胎儿舌的高度、长度和宽度、舌形指数(TSI,高度与长度之比)以及观察舌是否接触后咽壁。
共纳入116名受试者,MRI时平均孕周为25.6±5.1周:RS组27例(23%);小颌畸形组35例(30%);对照组54例(47%)。RS组的舌长度显著较短(P = 0.009),TSI显著较大(P < 0.0001)。RS组中有5例(19%)舌接触后咽壁,其他组无此情况(P < 0.0001)。
与孤立性小颌畸形胎儿和对照组相比,出生后患有RS的胎儿在子宫内的舌形状和位置有显著差异。产前MRI舌特征可能是出生后RS的预测指标。