MR Angiography of Moyamoya Disease Before and After Encephaloduroarteriosynangiosis
Hye-Kyung Yoon1,
Hyung-Jin Shin2,
Munhyang Lee3,
Hong Sik Byun1,
Dong Gyu Na1 and
Bokyung Kim Han1
1
Department of Radiology, Samsung Medial Center, Sungkyunkwan University School
of Medicine, 50 Irwon-Dong, Kangnam-Gu, Seoul 135-230, Koreay.
2
Department of Neurosurgery, Samsung Medial Center, Sungkyunkwan University
School of Medicine, Seoul 135-230 Korea.
3
Department of Pediatrics, Samsung Medial Center, Sungkyunkwan University
School of Medicine, Seoul, 135-230, Korea.

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Fig. 1. 2-year-old boy with moyamoya disease.
A, Conventional angiogram shows mild stenosis (arrows) of
both supraclinoid internal carotid arteries (ICAs). Severe stenosis of middle
cerebral artery (MCA) and anterior cerebral artery (ACA) is noted. Posterior
cerebral artery was normal (not shown). Degree of moyamoya vessels (MMVs) is
mild bilaterally.
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Fig. 1. 2-year-old boy with moyamoya disease.
B, Axial projected three-dimensional time-of-flight MR angiogram
shows severe stenosis (arrows) of ICAs, MCAs, and ACAs. Degree of
MMVs is mild bilaterally and well correlated with A. Vascular supply in
MCA territory was interpreted as fair bilaterally.
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Fig. 1. 2-year-old boy with moyamoya disease.
C, Follow-up MR angiogram obtained 6 months after right
encephaloduroarteriosynangiosis (EDAS) and 10 months after left EDAS shows
good transdural collateral vessels (arrowheads) supplying MCA
territories, which was interpreted as good bilaterally. Postoperative
neurologic status was good for both hemispheres.
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Fig. 2. 10-year-old girl with unilateral moyamoya disease.
A, Axial projected three-dimensional time-of-flight MR angiogram
shows total occlusion of right distal internal carotid artery, anterior
cerebral artery, and middle cerebral artery (MCA). Right MCA vascular supply
is poor compared with uninvolved left side. Moyamoya vessels (MMVs) are
prominent (arrows).
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Fig. 2. 10-year-old girl with unilateral moyamoya disease.
B, Follow-up MR angiogram obtained 4 months after surgery shows
development of transdural collateral vessels (arrowheads) to right
MCA territory, which was interpreted as good. Right superficial temporal
artery (arrow) is prominent. Interval decrease in MMVs is noted.
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Fig. 3. 3-year-old boy with poor clinical outcome after
encephaloduroarteriosynangiosis (EDAS).
A, Axial projected three-dimensional time-of-flight MR angiogram
shows severe stenosis of right internal carotid artery (ICA) and near total
occlusion of left ICA, consistent with moyamoya disease. Posterior cerebral
artery is normal and moyamoya vessels (MMVs) are mild bilaterally. Right
middle cerebral artery (MCA) vascular supply is fair, whereas left MCA
vascular supply is poor.
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Fig. 3. 3-year-old boy with poor clinical outcome after
encephaloduroarteriosynangiosis (EDAS).
B, Follow-up MR angiogram obtained 3 months after left EDAS and 2
months after right EDAS shows poor vascular supply in right MCA territory. ICA
stenosis has progressed and MMVs are decreased, suggesting disease
progression. Postoperative evaluation for neurologic status revealed poor
outcome for both sides.
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Fig. 4. 7-year-old boy with prominent superficial temporal artery after
encephaloduroarteriosynangiosis (EDAS).
A, Anteroposterior MR angiogram shows both superficial temporal
arteries (STAs) are barely visible (arrows).
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Fig. 4. 7-year-old boy with prominent superficial temporal artery after
encephaloduroarteriosynangiosis (EDAS).
B, Follow-up MR angiogram obtained 11 months after right EDAS and 9
months after left EDAS shows markedly enlarged STAs bilaterally
(arrows).
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