EC Gynaecology

Research Article Volume 13 Issue 9 - 2024

Fetal Cerebral Lamination in Cytomegalovirus-Infected Fetuses

Bart De Keersmaecker1,2, Filip Claus3, Michael Aertsen4 and Luc De Catte1*

1Department of Obstetrics and Gynecology, Fetal Medicine Unit, University Hospital Leuven, Belgium

2Department of Obstetrics and Gynaecology, AZ Groeninge, Kortrijk, Belgium

3Department of Radiology, OLV Ziekenhuis, Aalst, Belgium

4Department of Radiology, University Hospital Leuven, Belgium

*Corresponding Author: Luc De Catte, Feto-Maternal Medicine, University Hospital Leuven, Belgium.
Received: August 23, 2024; Published: September 12, 2024



Objectives: This study aimed to assess qualitatively and quantitatively the laminar organization of the cerebral cortex by prenatal ultrasound and MRI in cytomegalovirus-infected fetuses.

Methods: A retrospective study was conducted in 18 fetuses with a positive CMV PCR-analysis of amniotic fluid. All cases underwent serial ultrasound scans and at least one MR study before 28 weeks of gestation. Eleven cases with prenatal ultrasound diagnosis of CMV infection leading to termination were compared with the 7 cases going to term.

MRI detected 2 patterns of abnormal cerebral lamination: focal disruption of lamination and abnormal intermediate zone. On ultrasound, the laminar structure was visible as the interface between the subplate zone and the intermediate zone, quantitatively evaluated by measuring the distances between the different layers.

Results: In the TOP group, MRI showed focal disruption of lamination and abnormal intermediate zone in 3/11 and 11/11 cases respectively. In the TERM group, none of them had a disruption of lamination on MRI, however 3 had an abnormal intermediate zone.

On ultrasound, the posterior horn of the lateral ventricle was significantly larger in the TOP group compared to the TERM group. Measurement of the thickness of the subplate zone relative to the intermediate zone did not significantly differ between both groups.

Conclusion: The lamination pattern of the fetal brain can be evaluated qualitatively on MRI and ultrasound before 28 weeks and may indicate abnormal brain development in CMV-infected fetuses. Quantitative differences in lamination were not demonstrated on ultrasound.

 Keywords: Cytomegalovirus; Lamination; Fetal MRI; Fetal Ultrasound; Brain

  1. Garel C., et al. “Fetal MRI: normal gestational landmarks for cerebral biometry, gyration, myelination”. Child's Nervous System 7-8 (2003): 422-425.
  2. Kostovic I., et al. “Laminar organization of human fetal cerebrum revealed by histochemical markers and magnetic resonance imaging”. Cerebral Cortex5 (2002): 536-544.
  3. Prayer D., et al. “MRI of normal fetal brain development”. European Journal of Radiology 2 (2006): 199-216.
  4. Pugash D., et al. “Sonographic assessment of normal and abnormal patterns of fetal cerebral lamination”. Ultrasound in Obstetrics and Gynecology 6 (2012): 642-651.
  5. Robinson A and Endenes M. “Fetal neuro-imaging: an update on technical advances and clinical findings”. Pediatric Radiology 4 (2018): 471-485.
  6. Cannon M and Pellet P. “Risk of congenital cytomegalovirus infection”. BMC Public Health 5 (2005): 70.
  7. Maniclal S., et al. “The silent global burden of congenital cytomegalovirus”. Clinical Microbiology Reviews 1 (2013): 86-102.
  8. Revello M and Gerna G. “Diagnosis and management of human cytomegalovirus infection in the mother, fetus and newborn infant”. Clinical Microbiology Reviews 4 (2002): 680-715.
  9. Fowler K., et al. “The outcome of congenital cytomegalovirus infection in relation to maternal antibody status”. New England Journal of Medicine 10 (1992): 663-667.
  10. Kenneson A and Cannon M. “Review and meta-analysis of the epidemiology of congenital cytomegalovirus (CMV) infection”. Reviews in Medical Virology 4 (2007): 253-276.
  11. Koyano S., et al. “Dried umbilical cords in the retrospective diagnosis of congenital cytomegalovirus infection as a cause of developmental delays”. Clinical Infectious Diseases 10 (2009): e93-e95.
  12. Lanari M., et al. “Neonatal cytomegalovirus blood load and risk of sequellae in symptomatic and asymptomatic infected newborns”. Pediatrics1 (2006): 76-83.
  13. Dollard S., et al. “New estimates of prevalence of neurological and sensory sequelae and mortality associated with congenital cytomegalovirus infection”. Reviews in Medical Virology 5 (2007): 355-363.
  14. Malinger G., et al. “Imaging of fetal cytomegalovirus infection”. Fetal Diagnosis and Therapy 2 (2011): 117-126.
  15. Marques Diaz M., et al. “Prenatal cytomegalovirus disease and cerebral microgyria: evidence for perfusion failure, not disturbance of histogenesis, as the major cause of fetal cytomegalovirus encephalopathy”. Neuropediatrics 1 (1984): 18-24.
  16. Perlman J and Argyle C. “Lethal cytomegalovirus infections in preterm infants: clinical, radiological and neuropathological findings”. Annals of Neurology 1 (1992): 64-68.
  17. Lanari M., et al. “Neuroimaging in CMV congenital infected neonates: how and when”. Early Human Development 2 (2012): S3-S5.
  18. Romero D., et al. “Genetics and mechanisms leading to human cortical malformations”. Seminars in Cell and Developmental Biology 76 (2018): 33-75.
  19. Neu N., et al. “TORCH infections”. Clinics in Perinatology 1 (2015): 77-103.

Luc De Catte., et al. "Fetal Cerebral Lamination in Cytomegalovirus-Infected Fetuses". EC Gynaecology 13.9 (2024): 01-07.