Pd. Griffiths et al., ABNORMAL OCULAR ENHANCEMENT IN STURGE-WEBER SYNDROME - CORRELATION OFOCULAR MR AND CT FINDINGS WITH CLINICAL AND INTRACRANIAL IMAGING FINDINGS, American journal of neuroradiology, 17(4), 1996, pp. 749-754
Citations number
14
Categorie Soggetti
Clinical Neurology","Radiology,Nuclear Medicine & Medical Imaging
PURPOSE: To estimate the prevalence of abnormal ocular enhancement in
children with Sturge-Weber syndrome as detected with MR imaging and CT
and to correlate this with the clinical, fundoscopic, and intracrania
l imaging findings. METHODS: Fifteen children, 4 years old or younger,
with Sturge-Weber syndrome were examined with enhanced CT and MR imag
ing. Eleven children had unilateral intracranial involvement and 4 had
bilateral involvement, for a total of 19 abnormal hemispheres and rel
ated orbits. The presence of ocular enhancement was compared with the
fundoscopic findings independently. Ocular enhancement was correlated
with the extent of leptomeningeal disease, the severity of the cutaneo
us lesion, and the presence of glaucoma by the calculation of likeliho
od ratios and 95% confidence limits. RESULTS: Seven of the 15 patients
had abnormal ocular enhancement, which was present in 10 (53%) of the
eyes associated with the 19 abnormal hemispheres. MR imaging showed c
horoidal hemangioma in 7 of 8 patients in whom hemangiomas were shown
at fundoscopy. The likelihood of ocular enhancement was increased with
the presence of bilateral disease, extensive facial nevi, and glaucom
a; there was no significant correlation with the extent of hemispheric
involvement. CONCLUSION: Both enhanced MR imaging and CT can show dif
fuse choroidal hemangioma in patients with Sturge-Weber syndrome. Howe
ver, MR imaging is more sensitive and is recommended to aid in the det
ection of abnormalities with preventable late complications.