Département d'Imagerie Pédiatrique et Foetale, Hôpital Femme Mère Enfant, Lyon Bron, France.
Ultrasound Obstet Gynecol. 2014 Mar;43(3):346-52. doi: 10.1002/uog.12498. Epub 2014 Jan 2.
In order to illustrate the significance of a new anatomical finding, distortion of the interhemispheric fissure (DIHF) associated with impacted medial borders of the frontal lobes, we report a retrospective observational study of 13 fetuses in which DIHF was identified on prenatal imaging. In 10 cases there were associated anatomical anomalies, including mainly midline anomalies (syntelencephaly (n=2), lobar holoprosencephaly (n=1), Aicardi syndrome (n=2)), but also schizencephaly (n=1), cortical dysplasia (n=1) and more complex cerebral malformations (n=3), including neural tube defect in two cases. Chromosomal anomaly was identified in two cases, including 6p deletion in a case without associated central nervous system anomalies and a complex mosaicism in one of the cases with syntelencephaly. In two cases, the finding was apparently isolated on both pre- and postnatal imaging, and the children were doing well at follow-up, aged 4 and 5 years. The presence of DIHF on prenatal imaging may help in the diagnosis of cerebral anomalies, especially those involving the midline. If DIHF is apparently isolated on prenatal ultrasound, magnetic resonance imaging is recommended for careful analysis of gyration and midline, especially optic and olfactory structures. Karyotyping is also recommended.
为了说明与额叶内侧缘嵌入相关的半球间裂扭曲(DIHF)这一解剖学新发现的意义,我们报告了一项回顾性观察研究,纳入了 13 例产前影像学检查中发现 DIHF 的胎儿。其中 10 例存在相关的解剖学异常,主要包括中线异常(并脑(n=2)、叶型全前脑(n=1)、Aicardi 综合征(n=2)),也包括脑裂畸形(n=1)、皮质发育不良(n=1)和更复杂的脑畸形(n=3),包括 2 例神经管缺陷。2 例存在染色体异常,包括 1 例无伴发中枢神经系统异常的 6p 缺失和 1 例伴并脑的复杂镶嵌性。2 例患儿的发现显然在产前和产后影像学上均为孤立性表现,随访时年龄分别为 4 岁和 5 岁,目前情况良好。产前影像学上出现 DIHF 可能有助于诊断脑畸形,尤其是中线相关的脑畸形。如果产前超声检查中 DIHF 表现为孤立性,建议行磁共振成像检查以仔细分析脑回和中线,尤其是视路和嗅路结构。建议行核型分析。