
PRESUMED UNILATERAL VOGT-KOYANAGI-HARADA DISEASE-CASE REPORT OF A RARE CLINICAL ENTITY.
Abstract
In this retrospective report, we present a case of unilateral Vogt-Koyanagi-Harada (VKH) disease. This patient was evaluated with clinical, ophthalmological and laboratory examinations. The response following corticosteroid administration was evaluated. She had the characteristic clinical features of VKH involving only one eye, including disc edema, multiple sub retinal yellow lesions and exudative retinal detachment. This case indicates that the clinical and angiographic features were typical of VKH disease despite the unilateral involvement. Reports of unilateral VKH are meagre and we here report one of this rarity.
Full Text:
PDFReferences
Middle East Afr J Ophthalmol. 2011 Jan-Mar; 18(1): 82–84.doi: 10.4103/0974-9233.75898 PMCID: PMC3085163.Unilateral Vogt-Koyanagi-Harada Disease: Report of Two Cases Alok Agrawal and Jyotirmay Biswas1
Graefes Arch Clin Exp Ophthalmol. 2009 Aug; 247(8):1127-32. doi: 10.1007/s00417-009-1068-8. Epub 2009 Mar 24.Presumed Vogt-Koyanagi-Harada disease with unilateral ocular involvement: report of three cases. Usui Y1, Goto H, Sakai J, Takeuchi M, Usui M, Rao NA. Case Rep Ophthalmol. 2015 Oct 30;6(3):361-365.
Unilateral Vogt-Koyanagi-Harada Disease: A Clinical Case Report. Neves A1, Cardoso A2, Almeida M1, Campos J1, Campos A1, Castro Sousa JP1
Rajendram R, Evans M, Rao NA. Vogt-Koyanagi-Harada disease. Int Ophthalmol Clin. 2005
Spring. 45(2):115-34.
Uveitis-Fundamentals and clinical Practice:By Robert B. Nussenblatt, MD and Scott M. Whitcup, MD.
Refbacks
- There are currently no refbacks.

This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License.
An Initiative of The Tamil Nadu Dr MGR Medical University