Posterior Fossa Anomalies: A Detailed Review of Prenatal Findings and Management from a Tertiary Care Center.

IF 1.7 3区 医学 Q3 OBSTETRICS & GYNECOLOGY
Tanisha Gupta, K Aparna Sharma, Vatsla Dadhwal, Anubhuti Rana, Neerja Gupta, Madhulika Kabra, Rashmi Shukla, Saloni Kamboj, Smita Manchanda
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Abstract

Introduction: Posterior fossa anomalies (PFAs) encompass a spectrum of central nervous system malformations affecting the cerebellum, brainstem, and surrounding cerebrospinal fluid spaces. This study evaluates the prenatal diagnosis, genetic findings, and pregnancy outcomes of PFAs in a tertiary care setting in India.

Methods: A retrospective analysis was conducted on 35 cases of PFAs diagnosed via prenatal ultrasound and fetal MRI between January 2023 and May 2024. Anomalies were classified based on standard criteria, and genetic testing (karyotype, chromosomal microarray analysis, and whole-exome sequencing) was offered. Pregnancy outcomes, including termination, live birth, and neonatal survival, were documented, with short-term neurodevelopmental follow-up conducted via telephonic inquiries.

Results: The most common PFAs identified were vermian agenesis/hypoplasia (VH) and cerebellar hypoplasia, each accounting for 25.71% of cases, followed by Dandy-Walker malformation (20%). Isolated PFAs were observed in 37.14% of cases, while 62.85% had additional anomalies. Genetic testing was performed in 74.2% of cases, revealing variants in 5.71%. Karyotyping was performed in all tested cases and yielded normal results, while additional molecular testing with chromosomal microarray analysis (5 cases) and whole-exome sequencing (3 cases) detected clinically relevant variants in selected fetuses with PFAs. Among the 35 pregnancies, 65.71% opted for termination, facilitated by the Medical Termination of Pregnancy (MTP) Act, particularly for cases diagnosed beyond 24 weeks of gestation. Of the 9 live births, 2 neonates with VH (5.71%) died within 1 month, while 6 (17.14%) had normal developmental milestones at 6 months including 6 babies with mega cisterna magna and one with an arachnoid cyst. One infant exhibited delayed milestones.

Conclusion: PFAs are present with diverse prognostic implications, necessitating detailed imaging, genetic evaluation, and individualized counseling. The MTP Amendment Act played a crucial role in providing extended access to termination in pregnancies with severe PFAs and poor prognoses.

后窝畸形:详细审查产前发现和管理从三级保健中心。
目的:后窝异常(PFAs)包括一系列影响小脑、脑干和周围脑脊液间隙的中枢神经系统畸形。本研究评估产前诊断,遗传发现和妊娠结局的PFAs在印度三级保健设置。方法:回顾性分析2023年1月至2024年5月期间通过产前超声和胎儿MRI诊断的35例PFAs。根据标准标准对异常进行分类,并提供基因检测(核型,染色体微阵列分析和全外显子组测序)。记录妊娠结局,包括终止妊娠、活产和新生儿存活率,并通过电话询问进行短期神经发育随访。结果:最常见的PFAs为蠕虫发育/发育不全(VA/VH)和小脑发育不全(CH),各占25.71%,其次为Dandy-Walker畸形(20%)。37.14%的病例有孤立性PFAs, 62.85%的病例有附加异常。74.2%的病例进行了基因检测,5.71%的病例发现变异。对所有检测病例进行核型分析,结果均正常,而对选择的后窝异常胎儿进行染色体微阵列分析(5例)和全外显子组测序(3例)的分子检测,发现了临床相关的变异。在35例怀孕中,65.71%的人选择终止妊娠,这是在《医疗终止妊娠法》的推动下进行的,特别是在怀孕24周以上确诊的情况下。9例活产婴儿中,蠕虫发育不全2例(5.71%)在1个月内死亡,6例(17.14%)在6个月时发育正常,其中6例为大池,1例为蛛网膜囊肿。一名婴儿表现出发育里程碑延迟。结论:PFAs具有多种预后影响,需要详细的影像学检查、遗传评估和个体化咨询。MTP修正案在为严重PFAs和预后不良的妊娠提供更广泛的终止妊娠途径方面发挥了关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Fetal Diagnosis and Therapy
Fetal Diagnosis and Therapy 医学-妇产科学
CiteScore
4.70
自引率
9.10%
发文量
48
审稿时长
6-12 weeks
期刊介绍: The first journal to focus on the fetus as a patient, ''Fetal Diagnosis and Therapy'' provides a wide range of biomedical specialists with a single source of reports encompassing the common discipline of fetal medicine.
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