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因非腭裂指征进行产前磁共振成像检查时隐匿性腭裂的发生率。

Incidence of occult cleft palate on prenatal magnetic resonance images obtained for non-cleft indications.

作者信息

Resnick C M, Paige A, Jindal S, Gordon A M, Estroff J A

机构信息

Harvard School of Dental Medicine and Harvard Medical School, Boston, MA, USA; Department of Plastic and Oral Surgery, Boston Children's Hospital, Boston, MA, USA.

Harvard School of Dental Medicine and Harvard Medical School, Boston, MA, USA.

出版信息

Int J Oral Maxillofac Surg. 2023 May;52(5):560-563. doi: 10.1016/j.ijom.2022.09.006. Epub 2022 Sep 21.

Abstract

Prenatal diagnosis of craniofacial anomalies has improved family education and preparedness. Isolated cleft palate, however, remains difficult to identify sonographically. The aim of this study was to investigate the rate of incidental cleft palate identified on fetal magnetic resonance imaging (MRI) following the ultrasound detection of non-cleft abnormalities. This was a retrospective study of pregnant women who had fetal MRI performed between 2003 and 2017. To be included, the woman had to have been referred for fetal imaging for a non-cleft indication, with subsequent identification of an isolated cleft palate on MRI. Fetuses with a postnatal diagnosis of Robin sequence were excluded. The study sample included 30 women. Mean gestational age at MRI was 24 weeks 4 days± 38 days. Most referrals (76.7%) were for non-cleft craniofacial anomalies, of which micrognathia was the most common (63.3%). The annual incidence of occult cleft palate diagnosis was 0.4%, and a genetic syndrome was suspected based on imaging findings in 76.7%. Although rare, isolated cleft palate found incidentally on fetal imaging led to concern for a genetic syndrome in a high percentage of cases. This suggests that early referral for fetal MRI may provide critical information when sonographic fetal anomalies have been identified.

摘要

颅面畸形的产前诊断改善了家庭教育和准备工作。然而,孤立性腭裂在超声检查中仍难以识别。本研究的目的是调查在超声检测到非腭裂异常后,胎儿磁共振成像(MRI)偶然发现的腭裂发生率。这是一项对2003年至2017年间接受胎儿MRI检查的孕妇进行的回顾性研究。纳入标准为,孕妇因非腭裂指征接受胎儿影像学检查,随后MRI发现孤立性腭裂。出生后诊断为罗宾序列征的胎儿被排除。研究样本包括30名女性。MRI检查时的平均孕周为24周4天±38天。大多数转诊(76.7%)是因为非腭裂颅面畸形,其中小颌畸形最为常见(63.3%)。隐匿性腭裂诊断的年发生率为0.4%,76.7%的病例根据影像学表现怀疑有遗传综合征。尽管罕见,但胎儿影像学偶然发现的孤立性腭裂在很大比例的病例中引发了对遗传综合征的担忧。这表明,当超声发现胎儿异常时,早期转诊进行胎儿MRI检查可能会提供关键信息。

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