
VKHS is an inflammatory system disease with a subacute chronic course. It has a very variable, selective involvement of certain pigment cells of the eye, skin, inner ear, and meninges. Due in part to the fact that its symptoms are responsive to immunosuppressive therapy, pathogenesis as an autoimmune disease is considered. The clinical course of one of our patients is discussed. Early diagnosis of VKHS, although often very difficult, is mandatory for appropriate and timely treatment.
Adult, Male, Dose-Response Relationship, Drug, Magnetic Resonance Imaging, Drug Administration Schedule, Autoimmune Diseases, Cortisone, Diagnosis, Differential, Leukocyte Count, Azathioprine, Humans, Fluorescein Angiography, Visual Fields, Uveomeningoencephalitic Syndrome
Adult, Male, Dose-Response Relationship, Drug, Magnetic Resonance Imaging, Drug Administration Schedule, Autoimmune Diseases, Cortisone, Diagnosis, Differential, Leukocyte Count, Azathioprine, Humans, Fluorescein Angiography, Visual Fields, Uveomeningoencephalitic Syndrome
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