Fetal Ultrasound and Magnetic Resonance Imaging Findings in Suspected Septo‐Optic Dysplasia: A Diagnostic Dilemma. (2nd March 2020)

• Record Type: Journal Article
• Authors: Maduram, Amy; Farid, Nikdokht; Rakow‐Penner, Rebecca; Ghassemi, Neda; Khanna, Paritosh C.; Robbins, Shira L.; Hull, Andrew; Gold, Jeffrey; Pretorius, Dolores H.
• Is Part Of: Journal of ultrasound in medicine. Volume 39:Number 8(2020)
• Page Start: 1601
• Page End: 1614
• Publication Date: 2020-03-02
• Subjects: cavum septi pellucidi -- fetal magnetic resonance imaging -- fetal ultrasound -- optic nerve hypoplasia -- prenatal diagnosis -- septo‐optic dysplasia; Ultrasonics in medicine -- Periodicals; Ultrasonics; Ultrasonography; Ultrasonics in medicine; Electronic journals; Periodicals; Periodicals; 616.07543
• DOI: 10.1002/jum.15252
• Languages: English
• ISSNs: 0278-4297

Abstract

Abstract : Objectives: To investigate prenatal imaging findings supporting a diagnosis of suspected septo‐optic dysplasia (SOD) by fetal ultrasound (US), magnetic resonance imaging (MRI), or both. Methods: A retrospective review identified 11 patients with SOD: 9 had a clinical diagnosis of SOD postnatally, and 2 were terminated on the basis of suspicious prenatal imaging. Prenatal and neonatal imaging of the cavum septi pellucidi (CSP), frontal horns (FHs), and lateral ventricles was evaluated. Results: The appearance of the CSP varied on US and MRI. Complete ("fused") FHs or partial absence of the CSP was reported in 6 of 11 patients by fetal US and 7 of 8 patients by fetal MRI. The diagnosis of SOD was prospectively suspected prenatally in 6 of 11 and in an additional 5 of 11 cases retrospectively. Fetal MRI incorrectly initially reported normal morphologic abnormalities for 2 cases with partial absence of the CSP, whereas US accurately identified the morphologic abnormalities in 1 of these cases before MRI. Imaging features were first suggested at anatomic US (4 patients) and follow‐up prenatal US (2 patients). Neonatal imaging was concordant in all 9 live births: 5 completely absent CSP, 3 partially absent CSP, and 1 completely present CSP. Clinical manifestations included optic nerve hypoplasia (9 of 9), panhypopituitarism (5 of 9), and neurodevelopmental delays. Conclusions: Primary imaging features of SOD are "continuous" FHs with complete or partial absence of the CSP. Septo‐optic dysplasia can be suspected in utero and can appear isolated but has substantial associated central nervous system anomalies identified on fetal MRI or after birth. Partial absence of the CSP can be a prenatal sign of suspected SOD, although fetal MRI lacked the spatial resolution to identify it accurately in all cases.