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Research ArticlePediatricsF

Cervical and Intracranial Arterial Anomalies in 70 Patients with PHACE Syndrome

C.P. Hess, H.J. Fullerton, D.W. Metry, B.A. Drolet, D.H. Siegel, K.I. Auguste, N. Gupta, A.N. Haggstrom, C.F. Dowd, I.J. Frieden and A.J. Barkovich
American Journal of Neuroradiology November 2010, 31 (10) 1980-1986; DOI: https://doi.org/10.3174/ajnr.A2206
C.P. Hess
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H.J. Fullerton
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D.W. Metry
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B.A. Drolet
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D.H. Siegel
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K.I. Auguste
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N. Gupta
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A.N. Haggstrom
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C.F. Dowd
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I.J. Frieden
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A.J. Barkovich
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Abstract

BACKGROUND AND PURPOSE: Cerebral and cervical arterial abnormalities are the most common non-cutaneous anomaly in PHACE syndrome, but the location and type of arterial lesions that occur have not been systematically assessed in a large cohort. Our aim was to characterize the phenotypic spectrum of arteriopathy, assess the frequency with which different arteries are involved, and evaluate spatial relationships between arteriopathy, brain structural lesions, and hemangiomas in PHACE syndrome.

MATERIALS AND METHODS: Intracranial MRA and/or CTA images from 70 children and accompanying brain MR images in 59 patients with arteriopathy and PHACE syndrome were reviewed to identify the type and location of arterial lesions and brain abnormalities. Five categories of arteriopathy were identified and used for classification: dysgenesis, narrowing, nonvisualization, primitive embryonic carotid-vertebrobasilar connections, and anomalous arterial course or origin. Univariate logistic regression analyses were performed to test for associations between arteriopathy location, hemangiomas, and brain abnormalities.

RESULTS: By study design, all patients had arterial abnormalities, and 57% had >1 form of arteriopathy. Dysgenesis was the most common abnormality (56%), followed by anomalous course and/or origin (47%), narrowing (39%), and nonvisualization (20%). Primitive embryonic carotid-vertebrobasilar connections were present in 20% of children. Hemangiomas were ipsilateral to arteriopathy in all but 1 case. The frontotemporal and/or mandibular facial segments were involved in 97% of cases, but no other specific associations between arteriopathy location and hemangioma sites were detected. All cases with posterior fossa anomalies had either ICA anomalies or persistent embryonic carotid-basilar connections.

CONCLUSIONS: The arteriopathy of PHACE syndrome commonly involves the ICA and its embryonic branches, ipsilateral to the cutaneous hemangioma, with dysgenesis and abnormal arterial course the most commonly noted abnormalities. Brain abnormalities are also typically ipsilateral.

Abbreviations

ACA
anterior cerebral artery
AcomA
anterior communicating artery
AP
anteroposterior
BA
basilar artery
CTA
CT angiography
ICA
internal cerebral artery
MCA
middle cerebral artery
MRA
MR angiography
OMIM
Online Mendelian Inheritance in Man
PCA
posterior cerebral artery
PcomA
posterior communicating artery
PHA
persistent hypoglossal artery
PSA
persistent stapedial artery
PTA
persistent trigeminal artery
VA
vertebral artery
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American Journal of Neuroradiology: 31 (10)
American Journal of Neuroradiology
Vol. 31, Issue 10
1 Nov 2010
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Cite this article
C.P. Hess, H.J. Fullerton, D.W. Metry, B.A. Drolet, D.H. Siegel, K.I. Auguste, N. Gupta, A.N. Haggstrom, C.F. Dowd, I.J. Frieden, A.J. Barkovich
Cervical and Intracranial Arterial Anomalies in 70 Patients with PHACE Syndrome
American Journal of Neuroradiology Nov 2010, 31 (10) 1980-1986; DOI: 10.3174/ajnr.A2206

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Cervical and Intracranial Arterial Anomalies in 70 Patients with PHACE Syndrome
C.P. Hess, H.J. Fullerton, D.W. Metry, B.A. Drolet, D.H. Siegel, K.I. Auguste, N. Gupta, A.N. Haggstrom, C.F. Dowd, I.J. Frieden, A.J. Barkovich
American Journal of Neuroradiology Nov 2010, 31 (10) 1980-1986; DOI: 10.3174/ajnr.A2206
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