Your browser doesn't support javascript.
loading
The Significance of Fetal Brain Ventricular Asymmetry Without Dilation.
Meyer, Raanan; Bar-Yosef, Omer; Barzilay, Eran; Radinsky, Igal; Segal, Chen Key; Ziv-Baran, Tomer; Shani, Hagit; Levin, Gabriel; Katorza, Eldad.
Afiliación
  • Meyer R; Department of Obstetrics and Gynecology, Sheba Medical Center, Ramat-Gan, Israel.
  • Bar-Yosef O; Sackler School of Medicine, Tel Aviv University, Tel Aviv-Yafo, Israel.
  • Barzilay E; Sackler School of Medicine, Tel Aviv University, Tel Aviv-Yafo, Israel.
  • Radinsky I; Pediatric Neurology Unit, Sheba Medical Center, Ramat-Gan, Israel.
  • Segal CK; Department of Obstetrics and Gynecology, Samson Assuta Ashdod University Hospital, Ashdod, Israel.
  • Ziv-Baran T; Sackler School of Medicine, Tel Aviv University, Tel Aviv-Yafo, Israel.
  • Shani H; School of Medicine, Semmelweis University, Budapest, Hungary.
  • Levin G; Sackler School of Medicine, Tel Aviv University, Tel Aviv-Yafo, Israel.
  • Katorza E; Department of Obstetrics and Gynecology, Sheba Medical Center, Ramat-Gan, Israel.
J Ultrasound Med ; 40(11): 2413-2419, 2021 Nov.
Article en En | MEDLINE | ID: mdl-33427340
ABSTRACT

OBJECTIVES:

Fetal brain non-dilated ventricular asymmetry (NDVA) is a common finding on prenatal ultrasound exams. However, the optimal prenatal management in these cases remains unknown. We aimed to evaluate the benefit of prenatal genetic and magnetic resonance imaging (MRI) exams performed in cases of fetal NDVA detected on ultrasound.

METHODS:

A historical cohort study from a tertiary medical center. Singleton pregnancies with fetal brain NDVA diagnosed on ultrasound were included. We defined ventricular asymmetry as a difference of ≥2.0 mm between the lateral ventricles and ventricular dilation as ventricular width of >10.0 mm. Outcomes were evaluated with genetic exams (karyotype and chromosomal microarray analysis [CMA]) and fetal brain MRI.

RESULTS:

During the study period, there were 145 cases diagnosed with NDVA on ultrasound that comprised the cohort study. The rate of abnormal karyotype was 1.8% (1/56) and of abnormal CMA was 10% (3/30). The rate of minor additional CNS findings did not differ between ultrasound and MRI (3.4 versus 2.8%, respectively, p = .74). No major additional fetal brain findings were detected on MRI performed after ultrasound.

CONCLUSIONS:

In cases diagnosed with NDVA on ultrasound, no significant additional anomalies were detected on fetal brain MRI. The rate of abnormal genetic tests was relatively high and warrants further studies.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Diagnóstico Prenatal / Imagen por Resonancia Magnética Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Female / Humans / Pregnancy Idioma: En Revista: J Ultrasound Med Año: 2021 Tipo del documento: Article País de afiliación: Israel

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Diagnóstico Prenatal / Imagen por Resonancia Magnética Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Female / Humans / Pregnancy Idioma: En Revista: J Ultrasound Med Año: 2021 Tipo del documento: Article País de afiliación: Israel