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PO263 Moyamoya disorder a north-west england experience

Authors :
TP Enevoldsen
AK Sinha
C Malluci
John Williamson
D Rajashekar
A Visca
Ranjith Menon
Manish Bhojak
Alakendu Sekhar
Hans Nahser
Source :
Journal of Neurology, Neurosurgery & Psychiatry. 88:A81.3-A81
Publication Year :
2017
Publisher :
BMJ, 2017.

Abstract

Background Moyamoya disorder is a progressive intracranial cerebrovascular disease of unknown aetiology. The Walton Centre is a tertiary neuroscience centre serving a population of 3.5 million, Alder Hey Children’s Hospital is a tertiary paediatric hospital. Aim To compare stroke type, radiological features and clinical outcome in paediatric and adult population with Moyamoya disorder. Methodology Retrospective case note review of patients diagnosed with Moyamoya disorder at both sites from January 2007 to December 2016. Results 27 adults and 9 paediatric patients were identified. 5 of the adult patients presented during childhood. Mean age of presentation was 39 in the adult cohort and 7 in the paediatric cohort. Female to male ratio was 2:1. A majority were Caucasian. The commonest presentation in both groups was ischaemic stroke. Unilateral radiological features were seen in a majority of adult patients compared to bilateral features in paediatric cohort. 11 of the patients were managed surgically with procedures including EC-IC bypass and encephaloduroarteriosynangiosis. Conclusion This study demonstrated that a majority adult cohort had ischaemic stroke with unilateral radiological features and majority paediatric population had bilateral moyamoya disease. We conclude that the primary pathogenesis is likely to be different in the adult and paediatric population.

Details

ISSN :
1468330X and 00223050
Volume :
88
Database :
OpenAIRE
Journal :
Journal of Neurology, Neurosurgery & Psychiatry
Accession number :
edsair.doi...........5c5d677838fbed708dcb1cb07bc256ab
Full Text :
https://doi.org/10.1136/jnnp-2017-abn.282