Background: Vogt-Koyanagi-Harada Syndrome (VKHS) is a systemic disorde
r consisting of bilateral panuveitis with associated cutaneous and neu
rologic findings. In the absence of extraocular manifestations, diagno
sis of VKHS may be difficult. Methods: The results of magnetic resonan
ce imaging (MRI) in two patients with VKHS and of computed tomography
(CT) in a third patient with VKHS are described. Results: Bilateral, d
iffuse choroidal thickening with scleral sparing was the norm. Choroid
al thickening was demonstrable, despite the normal fundus appearance a
nd fluorescein angiogram, in one eye. Intense enhancement after admini
stration of gadopentetate was seen in the acute stages, but not after
corticosteroid treatment. High-intensity periventricular lesions were
seen in one patient. Conclusion: MRI superbly discriminates the fibrou
s sclera from the choroid and allows for the detection of subclinical
ocular and central nervous system disease. It is therefore a useful ad
junct in the diagnosis and follow-up of VKHS.