Pe. Burrows et al., CEREBRAL VASCULOPATHY AND NEUROLOGIC SEQUELAE IN INFANTS WITH CERVICOFACIAL HEMANGIOMA - REPORT OF 8 PATIENTS, Radiology, 207(3), 1998, pp. 601-607
PURPOSE: To determine the association of cerebral arterial anomalies a
nd progressive cerebral arterial occlusive disease in infants with fac
ial hemangiomas.MATERIALS AND METHODS: The cases of eight infants (sev
en girls and one boy) with the diagnosis of cervicofacial hemangioma a
nd intracranial arterial anomalies were reviewed retrospectively. Find
ings from clinical and imaging examination - including cranial compute
d tomography, magnetic resonance imaging and angiography, and catheter
angiography - were evaluated. Serial imaging findings were studied to
document progressive intracranial vascular changes. RESULTS: Five pat
ients had additional associated congenital anomalies. Seven were treat
ed with corticosteroid, interferon alfa-2a, or both. Progressive cereb
rovascular occlusive changes were documented in four of the seven pati
ents with serial imaging findings. Four other patients (all treated ph
armacologically) had MR imaging documentation of cerebral infarction,
and all had consistent, acquired neurologic symptoms. CONCLUSION: Intr
acranial arterial anomalies can coexist with cervicofacial hemangioma.
Aneurysmal and occlusive changes are potentially progressive and can
result in cerebral infarction. A causative association between occlusi
ve cerebrovascular disease and pharmacologic treatment has not been ex
cluded.