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Archives of Disease in Childhood - Fetal and Neonatal Edition 2003;88:F269-F274; doi:10.1136/fn.88.4.F269
Copyright © 2003 BMJ Publishing Group Ltd & Royal College of Paediatrics and Child Health.
Archives of Disease in Childhood Fetal and Neonatal Edition 2003;88:F269
© 2003 Archives of Disease in Childhood Fetal and Neonatal Edition

REVIEW

Magnetic resonance imaging of preterm brain injury

S J Counsell1, M A Rutherford1, F M Cowan2 and A D Edwards2

1 Robert Steiner Magnetic Resonance Unit, Imaging Sciences Department, MRC Clinical Sciences Centre
2 Department of Paediatrics, Faculty of Medicine, Imperial College, Hammersmith Campus, DuCane Road, London, UK

Correspondence to:
Correspondence to:
Professor A D Edwards, Department of Paediatrics, Faculty of Medicine, Imperial College, Hammersmith Campus, DuCane Road, London W12 OHS, UK;
david.edwards{at}ic.ac.uk

ABSTRACT

Magnetic resonance imaging (MRI) has proved to be a valuable tool for monitoring development and pathology in the preterm brain. This imaging modality is useful for assessing numerous pathologies including periventricular leukomalacia, intraventricular haemorrhage/germinal layer haemorrhage, and periventricular haemorrhagic infarction, and can help to predict outcome in these infants. MRI has also allowed the detection of posterior fossa lesions, which are not easily seen with ultrasound. Additionally, and perhaps most relevant, quantitative MR studies have shown differences between the normal appearing preterm brain at term equivalent age and term born infants, confirming that the brain develops differently in the ex utero environment. Further studies using quantifiable MR techniques will improve our understanding of the effects of the ex utero environment, including aspects of neonatal intensive care on the developing brain.

Keywords: magnetic resonance imaging; preterm brain injury

Abbreviations: ADC, apparent diffusion coefficient; CSE, conventional spin echo; DEHSI, diffuse excessive high signal intensity; DWI, diffusion weighted imaging; FSE, fast spin echo; GA, gestational age; GLH, germinal layer haemorrhage; IVH, intraventricular haemorrhage; MR, magnetic resonance; MRI, magnetic resonance imaging; PHI, periventricular haemorrhagic infarction; PVL, periventricular leukomalacia; 3D, three dimensional


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