TY - JOUR
T1 - Agenesis of the septum pellucidum
T2 - Prenatal diagnosis and outcome
AU - Borkowski-Tillman, Tamar
AU - Garcia-Rodriguez, Raquel
AU - Viñals, Fernando
AU - Branco, Miguel
AU - Kradjen-Haratz, Karina
AU - Ben-Sira, Liat
AU - Lerman-Sagie, Tally
AU - Malinger, Gustavo
N1 - Publisher Copyright:
© 2020 John Wiley & Sons, Ltd.
PY - 2020/5/1
Y1 - 2020/5/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85082604459&partnerID=8YFLogxK
U2 - 10.1002/pd.5663
DO - 10.1002/pd.5663
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C2 - 32037567
AN - SCOPUS:85082604459
SN - 0197-3851
VL - 40
SP - 674
EP - 680
JO - Prenatal Diagnosis
JF - Prenatal Diagnosis
IS - 6
ER -