Abstract
Objective: The aim of this study was to assess the additional value of diffusion-weighted magnetic
resonance imaging (DW-MRI) compared to conventional magnetic resonance imaging (MRI)
in new-born infants with arterial ischaemic stroke, with regard to the prediction
of neurodevelopmental outcome.
Methods: Neonatal DW-MRI data were available in 15 infants with a gestational age of ≥ 35
weeks and repeat MRI data were obtained in 12 of the 14 survivors. T1- and T2-weighted transverse images were obtained as well as 4-mm DWI slices. ADC maps were
calculated in manually selected regions on the basis of the DWI scans. All 14 survivors
were seen in the follow-up clinic and 12 were > 18 months when last seen.
Results: T2 hyperintensity was detected in the descending white matter tracts at the level of
the internal capsule in 7 infants and in only one of these also at the level of the
cerebral peduncles. Increased signal intensity (SI) was seen on DW-MRI in 8 infants
in the descending white matter tract ipsilateral to the territorial infarct at the
level of the internal capsule and in 5 of these also at the level of the cerebral
peduncles. ADC maps were available in 12 infants. ADC values were calculated at the
level of the cerebral peduncles, using the contralateral side as a reference value.
A significantly reduced value was found in 3 of the 5 infants who showed an increased
SI on DW-MRI. ADC maps were not available in the other two. Five of the seven infants
with abnormalities on DW-MRI/ADC of the corticospinal tracts developed a mild to moderate
hemiplegia, one showed an asymmetry of tone and one with only involvement of the anterior
part of the internal capsule was normal at follow-up. Wallerian degeneration, seen
at the level of the cerebral peduncles and/or the PLIC on the repeat MRI, was seen
in the 5 infants who had shown acute changes of the corticospinal tracts in the neonatal
period and who went on to develop motor sequelae.
Conclusions: Compared to MRI, DW-MRI and ADC maps provided additional, quantitative data of acute
corticospinal tract injury at an early time point after the insult, especially at
the level of the cerebral peduncles. The presence of increased SI on DW-MRI at the
level of the PLIC and the cerebral peduncles in new-born infants with arterial ischaemic
stroke is followed by Wallerian degeneration and subsequent development of hemiplegia.
Key words
Infarction - neonatal stroke - MRI - DW-MRI - Wallerian degeneration
References
- 1
Abdullah N D, Phillips M D, Matthews V P, Lowe M J.
Findings of descending motor fiber injury by diffusion weighted imaging in patients
with middle cerebral artery infarction.
AJR Am J Roentgenol.
1999;
172
66
- 2 Amiel-Tison C, Grenier A. Evaluation Neurologique du Nouveau-Né et du Nourisson. Paris;
Masson 1980
- 3
Battin M R, Dezoete A, Gunn T R, Gluckman P D, Gunn A J.
Neurodevelopmental outcome of infants treated with head cooling and mild hypothermia
after perinatal asphyxia.
Pediatrics.
2001;
107
480-484
- 4
Bouza H, Dubowitz L M, Rutherford M, Pennock J M.
Prediction of outcome in children with congenital hemiplegia: a magnetic resonance
study.
Neuropediatrics.
1994;
25
60-66
- 5
Castillo M, Mukherji S K.
Early abnormalities related to postinfarction Wallerian degeneration: evaluation with
MR diffusion-weighted imaging.
J Comput Assist Tomogr.
1999;
23
1004-1007
- 6
Claeys V, Deonna T, Chrzanowski R.
Congenital hemiparesis: the spectrum of lesions, a clinical and computerized tomographic
study.
Helv Paediatr Acta.
1983;
38
439-455
- 7
Cowan F M, Pennock J M, Hanrahan K P, Manji K P, Edwards D.
Early detection of cerebral infarction and hypoxic ischaemic encephalopathy in neonates
using diffusion weighted magnetic imaging.
Neuropediatrics.
1994;
25
172-175
- 8
De Vries L S, Groenendaal F, Eken P, van Haastert I C, Rademaker K J, Meiners L C.
Infarcts in the distribution of the middle cerebral artery in preterm and full-term
infants.
Neuropediatrics.
1997;
28
88-96
- 9
De Vries L S, Groenendaal F, Eken P, Rademaker K J, Meiners L C.
Asymmetrical myelination of the posterior limb of the internal capsule: an early predictor
of hemiplegia.
Neuropediatrics.
1999;
30
314-319
- 10 Dubowitz L MS, Dubowitz V. The Neurological Assessment of the Preterm and Full-Term
Infant. Clin Dev Med. No 79. London: SIMP/Heinemann, Philadelphia; Lippincott 1981
- 11
Estan J, Hope P.
Unilateral neonatal cerebral infarction in full-term infants.
Arch Dis Child Fetal Neonatal Edition.
1997;
76
F88-F93
- 12
Golomb M R, Dick P T, MacGregor D L, Armstrong D C, DeVeber G A.
Cranial ultrasonography has a low sensitivity for detecting arterial ischemic stroke
in term neonates.
J Child Neurol.
2003;
18
98-103
- 13
Govaert P, Matthys E, Zecic A. et al .
Perinatal cortical infarction within middle cerebral artery trunks.
Arch Dis Child Fetal Neonatal Edition.
2000;
82
F59-F63
- 14 Griffiths R. The abilities of babies: A Study in Mental Measurement. Amersham;
Association of Research in Infant and Child Development 1976
- 15
Inoue Y, Matsumara Y, Fukuda T, Nemoto Y, Shirahata N, Suzuki T. et al .
MR imaging of Wallerian degeneration in the brainstem: temporal relationships.
AJNR Am J Neuroradiol.
1990;
11
897-902
- 16
Kang D W, Chu K, Yoon B W, Song I C, Chang K H, Roh J K.
Diffusion-weighted imaging in Wallerian degeneration.
J Neurol Sci.
2000;
178
167-169
- 17
Krishnamoorthy K, Soman T, Takeoka M, Schaefer P.
Diffusion-weighted imaging in neonatal cerebral infarction: clinical utility and follow-up.
J Child Neurol.
2000;
15
592-602
- 18
Kuhn M J, Johnson K A, Davis K R.
Wallerian degeneration: evaluation with MR imaging.
Radiology.
1988;
168
199-202
- 19
Kuhn M J, Mikulis J, Ayoub D M, Kosofsky B E, Davis K R, Traveras J M.
Wallerian degeneration after cerebral infarction: evaluation with sequential MR imaging.
Radiology.
1989;
172
179-182
- 20
Kűker W, Mohrle S, Mader I, Schoning M, Nagele T.
MRI for the management of neonatal cerebral infarctions: importance of timing.
Childs Nerv System.
2004;
46
896-899
- 21
Ludwin S K, Bisby M A.
Delayed Wallerian degeneration in the central nervous system of Ola mice: an ultrastructural
study.
J Neurol Sci.
1992;
109
140-147
- 22
Lynch J K, Hirtz D G, DeVeber G, Nelson K B.
Report of the National Institute of Neurological Disorders and Stroke workshop on
perinatal and childhood stroke.
Pediatrics.
2002;
109
116-123
- 23
Mazumdar A, Mukherjee P, Miller J H, Malde H, McKinstry R C.
Diffusion-weighted imaging in acute corticospinal tract injury preceding Wallerian
degeneration in the maturing human brain.
AJNR Am J Neuroradiol.
2003;
24
1057-1066
- 24
McKinstry R C, Miller J H, Snyder A Z, Mathur A, Schefft G L, Almli C R. et al .
A prospective, longitudinal diffusion tensor imaging study of brain injury in newborns.
Neurology.
2002;
59
824-833
- 25
Mercuri E, Rutherford M, Cowan F, Pennock J, Counsell S, Papadimitriou M. et al .
Early prognostic indicators of outcome in infants with neonatal cerebral infarction:
a clinical, electroencephalographic and magnetic resonance imaging study.
Pediatrics.
1999;
103
39-46
- 26
Mercuri E, Cowan F, Gupte G, Manning R, Laffan M, Rutherford M. et al .
Prothrombotic disorders and abnormal neurodevelopmental outcome in infants with neonatal
cerebral infarction.
Pediatrics.
2001;
107
1400-1404
- 27
Mercuri E, Barnett A, Rutherford M, Guzzetta A, Haataja L, Cioni G. et al .
Neonatal cerebral infarction and neuromotor outcome at school age.
Pediatrics.
2004;
113
95-100
- 28
Merzbacher L.
Untersuchungen an winterschlafenden Fledermäusen: II. Mittheilung. Die Nervendegeneration
während des Winterschlafes. Die Beziehungen zwischen Temperatur and Winterschlaf [Investigations
on hibernating bats. 2nd communication. The relationship between temperature and hibernation].
Arch Ges Physiol Menschen Thiere.
1903;
100
568-585
- 29
Nelson K B, Lynch J K.
Stroke in new-born infants.
Lancet Neurology.
2004;
3
150-158
- 30
Pennock J M, Rutherford M A, Cowan M, Bydder G M.
MRI: early onset of changes in Wallerian degeneration.
Clin Radiol.
1993;
47
311-314
- 31
Ramaswamy V, Miller S P, Barkovich A J, Partridge J C, Ferriero D M.
Perinatal stroke in term infants with neonatal encephalopathy.
Neurology.
2004;
62
2088-2091
- 32
Roelants-van Rijn A M, Nikkels P GJ, Groenendaal F, van der Grond J, Barth P G, Snoeck I.
et al .
Neonatal diffusion-weighted MR imaging: relation with histopathology or follow-up
MR examination.
Neuropediatrics.
2001;
32
286-294
- 33
Rutherford M, Counsell S, Allsop J, Boardman J, Kapellou O, Larkman D. et al .
Diffusion-weighted magnetic resonance imaging in term perinatal brain injury: a comparison
with site of lesion and time from birth.
Pediatrics.
2004;
114
1004-1014
- 34 Touwen B LC. Examination of the Child with Minor Neurological Dysfunction. Clinics
in Developmental Medicine. No 71. London; SIMP/Heineman 1979
- 35
Uchino A, Imada H, Ohno M.
MR imaging of Wallerian degeneration in the human brain stem after ictus.
Neuroradiology.
1990;
32
191-195
- 36
Uchino A, Sawada A, Takase Y, Egashira R, Kudo S.
Transient detection of early Wallerian degeneration on diffusion-weighted MRI after
an acute cerebrovascular accident.
Neuroradiology.
2004;
46
183-188
- 37
Van der Toorn A, Dijkhuizen R M, Tulleken C A, Nicolay K.
Diffusion of metabolites in normal and ischemic rat brain measured by localized 1
H MRS.
Magn Reson Med.
1996;
35
914-922
- 38
Van Everdingen K J, van der Grond J, Kappelle L J, Ramos L MP, Mali W PTM.
Diffusion-weighted magnetic resonance imaging in acute stroke.
Stroke.
1998;
29
1783-1790
- 39
Waller A V.
Experiments on the section of the glosso-pharyngeal and hyoglossal nerves in the frog
and observations of the alterations produced thereby in the structure of their primitive
fibres.
Philosophical Transactions of the Royal Society London.
1850;
140
423-429
Prof. Dr. Linda S. de Vries
Department of Neonatology
Wilhelmina Children's Hospital
UMC Utrecht
KE 04.123.1
PO Box 85090
3508 AB Utrecht
The Netherlands
Email: l.devries@wkz.azu.nl