Case Report
Author Details :
Volume : 5, Issue : 2, Year : 2019
Article Page : 94-96
https://doi.org/10.18231/j.ijooo.2019.025
Abstract
Vogt Koyanagi Harada is a multisystem, granulomatous autoimmune disease with delayed onset of cutaneous manifestation. The case of an adolescent male with bilateral decreased vision is presented. The patient was diagnosed Vogt-Koyanagi-Harada (VKH) syndrome, with extraocular systemic manifestations in the form of sensory neural hearing loss (SNHL) and greying of scalp hairs at initial presentation which is very rare as cutaneous involvement usually occurs 2 to 3 months after the onset of disease. The syndrome may result in permanent visual loss but prompt treatment with corticosteroid therapy can restore vision. Therefore early ophthalmologic consultation must be sought.
Keywords: Vogt-Koyanagi-Harada, Sensory neural hearing loss, Greying hairs.
How to cite : Gupta V, Sharma K, Guleria P, Sharma R L, Bilateral Vogt-Koyanagi-Harada disease with poliosis (a rare initial presentation). IP Int J Ocul Oncol Oculoplasty 2019;5(2):94-96
This is an Open Access (OA) journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
Viewed: 1171
PDF Downloaded: 428