ultrasound Department, Guangdong Women and Children Hospital, Guangzhou, China.
Guangzhou Medical University, Guangzhou, China.
Prenat Diagn. 2023 Jun;43(6):763-772. doi: 10.1002/pd.6316. Epub 2023 Jan 29.
To describe the prenatal ultrasound (US) findings, genetic results, and clinical outcomes of fetuses with suspected agenesis of the septum pellucidum (ASP) in the Chinese population.
This retrospective, single-center study included a cohort of fetuses with ASP diagnosed by prenatal imaging over a 10-year period. We evaluated US findings, associated anomalies, genetic results, and clinical outcomes. Prenatal and postnatal imaging findings were compared as well as the clinical outcome of delivery.
Ninety patients were included, with a median follow-up time of 36 months (1-96 months). Thirty-six fetuses (40%) with isolated ASP were diagnosed by prenatal US or magnetic resonance imaging (MRI); 39 cases (43.3%) had ASP with central nervous system malformations and 15 cases (16.6%) had ASP with non-CNS abnormalities. Additional imaging findings were supplemented with prenatal MRI in 13 cases. Genetic tests were performed on 32 patients, of whom six had abnormalities. Prenatal US results of 40 patients (40/70) diagnosed by referral hospitals did not correspond to our findings. Of the 38 patients with postnatal records, 11 had abnormal neurological development.
CONCLUSION(S): The outcome of an isolated ASP is usually favorable; however, neurological developmental delay is commonly observed if it is combined with other malformations.
描述中国人群中疑诊无脑叶性透明隔发育不全(ASP)胎儿的产前超声(US)表现、遗传学结果和临床转归。
本回顾性单中心研究纳入了 10 年间经产前影像学诊断为 ASP 的胎儿队列。我们评估了 US 表现、相关畸形、遗传学结果和临床转归。比较了产前和产后影像学表现以及分娩的临床结局。
共纳入 90 例患者,中位随访时间为 36 个月(1-96 个月)。36 例(40%)胎儿经产前 US 或磁共振成像(MRI)诊断为单纯 ASP;39 例(43.3%)伴有中枢神经系统畸形,15 例(16.6%)伴有非 CNS 异常。13 例额外的影像学发现通过产前 MRI 补充。对 32 例患者进行了基因检测,其中 6 例存在异常。38 例有产后记录的患者中,11 例有神经发育异常。
单纯 ASP 的结局通常较好;然而,如果与其他畸形合并存在,则常见神经发育迟缓。