Agenesis of the septum pellucidum: Prenatal diagnosis and outcome. (31st March 2020)

• Record Type: Journal Article
• Authors: Borkowski‐Tillman, Tamar; Garcia‐Rodriguez, Raquel; Viñals, Fernando; Branco, Miguel; Kradjen‐Haratz, Karina; Ben‐Sira, Liat; Lerman‐Sagie, Tally; Malinger, Gustavo
• Is Part Of: Prenatal diagnosis. Volume 40:Number 6(2020)
• Page Start: 674
• Page End: 680
• Publication Date: 2020-03-31
• Subjects: Prenatal diagnosis -- Periodicals; Fetus -- Diseases -- Diagnosis -- Periodicals; Electronic journals; 618.32075
• DOI: 10.1002/pd.5663
• Languages: English
• ISSNs: 0197-3851

Abstract

Abstract: Objective: The purpose of this study is to describe the imaging findings in a group of fetuses with suspected agenesis of the septum pellucidum (ASP) and to evaluate their clinical outcome. Methods: This is a retrospective multicenter study on a cohort of fetuses diagnosed with suspected ASP, between 2008 and 2017. The records of each patient, including ultrasound (US) and magnetic resonance studies, were reviewed and compared with the postnatal findings. Results: Forty‐seven patients were included in the study at a mean gestational age of 26.6 weeks. In 17 patients, the ASP was considered isolated. Fourteen patients delivered live‐born, and all 14 are developing normally. Three were lost to follow‐up. Twenty‐four patients had associated malformations involving the central nervous system (CNS); 13 were delivered (normal development [5], abnormal [6] and no follow‐up [2]). Nine patients opted for termination, and two pregnancies were lost to follow‐up. Six patients had non‐CNS associated findings, two were delivered with normal neurological development and four had a termination. Conclusions: Isolated ASP is usually associated with a favorable outcome; but in the presence of associated malformations, there is at least a 50% risk of abnormal development. Current imaging techniques can provide an accurate prognosis in cases when ASP appears isolated.