Expanding the spectrum of human ganglionic eminence region anomalies on fetal magnetic resonance imaging
Creators
- 1. Children's Hospital ''V. Buzzi'', Department of Radiology and Neuroradiology, Milan (Italy)
- 2. Ospedale Maggiore Policlinico, Medical Genetics Unit, Fondazione I.R.C.C.S. Ca' Granda, Milan (Italy)
- 3. University of Milan, Department of Health Sciences, Milan (Italy)
- 4. Fondazione I.R.C.C.S. Istituto Neurologico ''C. Besta'', Clinical Epileptology and Experimental Neurophysiology Unit, Milan (Italy)
- 5. San Paolo Hospital, Division of Human Pathology, Milan (Italy)
- 6. Children's Hospital ''V. Buzzi'', Department of Obstetrics and Gynaecology, Prenatal Diagnosis, Milan (Italy)
Description
Ganglionic eminence (GE) is a transient fetal brain structure that harvests a significant amount of precursors of cortical GABA-ergic interneurons. Prenatal magnetic resonance (MR) imaging features of GE anomalies (i.e., cavitations) have already been reported associated with severe micro-lissencephaly. The purpose of this report was to illustrate the MR imaging features of GE anomalies in conditions other than severe micro-lissencephalies. Among all the fetuses submitted to prenatal MR imaging at our center from 2005 to 2014, we collected eight cases with GE anomalies and only limited associated brain anomalies. The median gestational age at the time of MR imaging was 21 weeks ranging from 19 to 29 weeks. Two senior pediatric neuroradiologists categorized the anomalies of the GE region in two groups: group one showing cavitation in the GE region and group two showing enlarged GE region. For each fetal case, associated cranial anomalies were also reported. Five out of the eight cases were included in group one and three in group two. Besides the GE region abnormality, all eight cases had additional intracranial anomalies, such as mild partial callosal agenesis, vermian hypoplasia and rotation, cerebellar hypoplasia, ventriculomegaly, enlarged subarachnoid spaces, molar tooth malformation. Ultrasound generally detected most of the associated intracranial anomalies, prompting the MR investigation; on the contrary in none of the cases, GE anomalies had been detected by ultrasound. Our observation expands the spectrum of human GE anomalies, demonstrating that these may take place also without associated severe micro-lissencephalies. (orig.)
Availability note (English)
Available from: http://dx.doi.org/10.1007/s00234-015-1622-5Additional details
Identifiers
Publishing Information
- Journal Title
- Neuroradiology
- Journal Volume
- 58
- Journal Issue
- 3
- Journal Page Range
- p. 293-300
- ISSN
- 0028-3940
- CODEN
- NRDYAB
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 47065523
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- BRAIN; CAVITATION; DIAGNOSIS; DIFFUSION; FETUSES; GANGLIONS; IMAGE PROCESSING; MALFORMATIONS; NERVE CELLS; NEUROLOGY; NMR IMAGING; ORIGIN; PREGNANCY; RELAXATION TIME; WEIGHTING FUNCTIONS
- Descriptors DEC
- ANIMAL CELLS; BODY; CENTRAL NERVOUS SYSTEM; DIAGNOSTIC TECHNIQUES; FUNCTIONS; MEDICINE; NERVOUS SYSTEM; ORGANS; PATHOLOGICAL CHANGES; PROCESSING; SOMATIC CELLS