The clinical spectrum of Vogt-Koyanagi-Harada syndrome: A single-center experience from South India

Authors

  • Padmamalini Mahendradas Narayana Nethralaya, Super Speciality Eye Hospital and Postgraduate Institute of Ophthalmology, Bangalore
  • Ankush Kawali Narayana Nethralaya
  • Neha Bharti Narayana Nethralaya
  • Dhawal Haria Narayana Nethralaya
  • Naren Shetty Narayana Nethralaya
  • Rohit Shetty Narayana Nethralaya
  • Bhujang K Shetty Narayana Nethralaya

DOI:

https://doi.org/10.15305/ijrci/v1iS1/55

Keywords:

Vogt- Koyanagi- Harada disease, Exudative Retinal Detachment, Sunset glow fundus, Poliosis, Vitiligo, Tinnitus, systemic Steroids, Systemic immunosuppressive therapy

Abstract

Aim

To report the clinical features, investigations, management, and outcome in typical cases of Vogt-Koyanagi-Harada Syndrome (VKH) in a tertiary eye care center in South India.

 

Materials and methods

Retrospective interventional case series of VKH patients.

 

Results

Seventy-one eyes of 36 patients (age range 12-68 years) were included. Anatomical diagnoses were posterior uveitis (15 eyes) and pan uveitis (56 eyes). The classification of the cases with regard to VKH disease was as follows: six eyes were classified as complete, 41 eyes as incomplete, and 24 eyes as probable VKH disease. Commonest extraocular manifestation noted in 25 cases was headache. The more common ocular presentations were disc hyperemia (40 eyes) and exudative retinal detachment in the posterior pole (46 eyes) and in the retinal periphery (24 eyes). All patients were managed on systemic steroids. Systemic immunosuppressive therapy was given in 21 cases. Majority of the participants had good visual outcome.

Conclusion

Early recognition and aggressive treatment of VKH disease result in good visual outcome in typical VKH cases.

Author Biography

Padmamalini Mahendradas, Narayana Nethralaya, Super Speciality Eye Hospital and Postgraduate Institute of Ophthalmology, Bangalore

Department of uveitis and Ocular Immunology

References

Fang W, Yang P. Vogt-koyanagi-harada syndrome. Current Eye Research. 2008;33(7):517-517.

Wakabayashi T, Morimura Y, Miyamoto Y, Okada AA. Changing patterns of intraocular inflammatory disease in Japan.OculImmunolInflamm. 2003;11:277-286.

Nashtaei EM, Soheilian M, Herbort CP, Yaseri M. Patterns of Uveitis in the Middle East and Europe. J Ophthalmic Vis Res. 2011 Oct;6(4):233-40.

Martin TD, Rathinam SR, Cunningham ET Jr. Prevalence, clinical characteristics, and causes of vision loss in children with Vogt-Koyanagi-Harada disease in South India. Retina (Philadelphia, Pa). 2010 Aug;30(7):1113-21.

Read RW, Holland GN, Rao NA, Tabbara KF, Ohno S, Arellanes-Garcia L, et al. Revised diagnostic criteria for Vogt-Koyanagi-Harada disease: report of an international committee on nomenclature. Am J Ophthalmol. 2001 May;131(5):647-52.

Rao NA. Pathology of Vogt-Koyanagi-Harada disease. Int Ophthalmol. 2007 Jun;27(2-3):81-5.

Khairallah M, Zaouali S, Messaoud R, Chaabane S, Attia S, Ben Yahia S, et al. The spectrum of Vogt-Koyanagi-Harada disease in Tunisia, North Africa. Int Ophthalmol. 2007 Jun;27(2-3):125-30.

Murthy SI, Moreker MR, Sangwan VS, Khanna RC, Tejwani S. The spectrum of Vogt-Koyanagi-Harada disease in South India. Int Ophthalmol. 2007 Jun;27(2-3):131-6.

Moorthy RS, Inomata H, Rao NA. Vogt-Koyanagi-Harada syndrome. Surv Ophthalmol. 1995 Jan-Feb;39(4):265-92.

P E Rubsamen JDG. Vogt-Koyanagi-Harada syndrome. Clinical course, therapy, and long-term visual outcome. Archives of ophthalmology. 1991;109(5):682-7.

Chee S-P, Jap A, Bacsal K. Spectrum of Vogt-Koyanagi-Harada disease in Singapore. Int Ophthalmol. 2007 Jun;27(2-3):137-42.

Kiyomoto C, Imaizumi M, Kimoto K, Abe H, Nakano S, Nakatsuka K. Vogt-Koyanagi-Harada disease in elderly Japanese patients. Int Ophthalmol. 2007 Jun;27(2-3):149-53.

Tugal-Tutkun I, Ozyazgan Y, Akova YA, Sullu Y, Akyol N, Soylu M, et al. The spectrum of Vogt-Koyanagi-Harada disease in Turkey: VKH in Turkey. Int Ophthalmol. 2007 Jun;27(2-3):117-23.

Beniz J, Forster DJ, Lean JS, Smith RE, Rao NA. Variations in clinical features of the Vogt-Koyanagi-Harada syndrome. Retina (Philadelphia, Pa). 1991;11(3):275-80.

RajendramR,Evans M,RaoNA.Vogt-Koyanagi-Harada Disease. Int Ophthalmol Clin. 2005; 45:115–134.

Fardeau C, Tran THC, Gharbi B, Cassoux N, Bodaghi B, LeHoang P. Retinal fluorescein and indocyanine green angiography and optical coherence tomography in successive stages of Vogt-Koyanagi-Harada disease. Int Ophthalmol. 2007 Jun;27(2-3):163-72.

Herbort CP, Mantovani A, Bouchenaki N. Indocyanine green angiography in Vogt-Koyanagi-Harada disease: angiographic signs and utility in patient follow-up. Int Ophthalmol. 2007 Jun;27(2-3):173-82.

Mondkar SV, Biswas J, Ganesh SK. Analysis of 87 cases with Vogt-Koyanagi-Harada disease. Jpn J Ophthalmol. 2000 Jun;44(3):296-301.

Belfort Junior R, Nishi M, Hayashi S, Abreu MT, Petrilli AM, Plut RC. Vogt-Koyanagi-Harada’s disease in Brazil. Jpn J Ophthalmol. 1988;32(3):344-7.

Downloads

Published

26-12-2013