Moyamoya disease in a child with previous acute necrotizing encephalopathy.

Abstract:

:A previously healthy 24-day-old boy presented with a 2-day history of fever and had a convulsion on the day of admission. MRI showed abnormal signal in the thalami, caudate nuclei and central white matter. Acute necrotising encephalopathy was diagnosed, other causes having been excluded after biochemical and haematological analysis of blood, urine and CSF. He recovered, but with spastic quadriparesis. At the age of 28 months, he suffered sudden deterioration of consciousness and motor weakness of his right limbs. MRI was consistent with an acute cerebrovascular accident. Angiography showed bilateral middle cerebral artery stenosis or frank occlusion with numerous lenticulostriate collateral vessels consistent with moyamoya disease.

journal_name

Pediatr Radiol

journal_title

Pediatric radiology

authors

Kim TK,Eun BL,Cha SH,Chung KB,Kim JH,Kim BH,Chung HH

doi

10.1007/s00247-003-0955-0

keywords:

subject

Has Abstract

pub_date

2003-09-01 00:00:00

pages

644-7

issue

9

eissn

0301-0449

issn

1432-1998

journal_volume

33

pub_type

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