Literature DB >> 28260142

The spectrum of Vogt-Koyanagi-Harada disease in Iran.

Alireza Hedayatfar1,2, Seyedeh Maryam Hosseini3, Nasser Karimi4, Khalil Ghasemi Falavarjani4, Negin Badie5, Mahsa Zameni6, Masoud Soheilian6.   

Abstract

PURPOSE: To report the spectrum of Vogt-Koyanagi-Harada (VKH) disease in Persians.
MATERIALS AND METHODS: This is a retrospective chart review of patients diagnosed with VKH disease at four referral centers in Iran. Patients' demographics, ocular and extraocular manifestations, treatment modalities, complications, and visual outcomes were collected and analyzed.
RESULTS: Eighty-eight patients with a mean age of 32.1 ± 12.6 years (range 7-79 years) were studied. Fifty-nine patients (67.0%) were female. Sunset glow fundus was seen in 40.9%, and nummular peripheral chorioretinal scars in 55.7% of eyes. Integumentary findings were noticed in 14.8% of the patients. In patients with acute presentation, exudative retinal detachment was the most common ocular finding (87.8%) followed by optic disk swelling (71.4%). Anterior uveitis and vitritis each were found in about half of the studied eyes. Auditory symptoms were reported by 38.8% of the patients. Overall, immunomodulatory agents were used in 72.7% of the patients. Ocular complications occurred in 36.4% of eyes (mean follow-up 3.8 years, range 6-228 months). Final visual acuity was 20/40 or better in 73.3% of eyes. Four patients (4.5%) were classified as having 'complete' type of the disease, 36 (40.9%) 'incomplete' type, and 48 (54.5%) 'probable' type.
CONCLUSION: In our series, there are clinical features that differ from those reported in other studies. While auditory symptoms occurred in more than one-third of patients, integumentary findings were rather rare. Most patients exhibited the 'probable' type of VKH disease. The overall visual prognosis was favorable.

Entities:  

Keywords:  Iran; Uveitis; VKH; Vogt–Koyanagi–Harada disease

Mesh:

Substances:

Year:  2017        PMID: 28260142     DOI: 10.1007/s10792-017-0478-6

Source DB:  PubMed          Journal:  Int Ophthalmol        ISSN: 0165-5701            Impact factor:   2.031


  21 in total

Review 1.  Vogt-Koyanagi-Harada disease.

Authors:  Russell W Read
Journal:  Ophthalmol Clin North Am       Date:  2002-09

2.  Revised diagnostic criteria for Vogt-Koyanagi-Harada disease: report of an international committee on nomenclature.

Authors:  R W Read; G N Holland; N A Rao; K F Tabbara; S Ohno; L Arellanes-Garcia; P Pivetti-Pezzi; H H Tessler; M Usui
Journal:  Am J Ophthalmol       Date:  2001-05       Impact factor: 5.258

3.  Vogt-Koyanagi-Harada syndrome. Clinical course, therapy, and long-term visual outcome.

Authors:  P E Rubsamen; J D Gass
Journal:  Arch Ophthalmol       Date:  1991-05

4.  Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients.

Authors:  Peizeng Yang; Yalin Ren; Bing Li; Wang Fang; Qianli Meng; Aize Kijlstra
Journal:  Ophthalmology       Date:  2006-11-21       Impact factor: 12.079

5.  Patterns of uveitis in a tertiary eye care center in Iran.

Authors:  Masood Soheilian; Kumars Heidari; Shahin Yazdani; Mohsen Shahsavari; Hamid Ahmadieh; Mohammad Dehghan
Journal:  Ocul Immunol Inflamm       Date:  2004-12       Impact factor: 3.070

6.  Vogt-Koyanagi-Harada disease: clinical and demographic characteristics of patients in a specialized eye hospital in Turkey.

Authors:  Pinar Ozdal; Yasemin Ozdamar; Alper Yazici; Mehmet Y Teke; Faruk Ozturk
Journal:  Ocul Immunol Inflamm       Date:  2013-12-11       Impact factor: 3.070

7.  Vogt-Koyanagi-Harada syndrome in children compared to adults.

Authors:  K F Tabbara; P S Chavis; W R Freeman
Journal:  Acta Ophthalmol Scand       Date:  1998-12

Review 8.  Standardization of uveitis nomenclature for reporting clinical data. Results of the First International Workshop.

Authors:  Douglas A Jabs; Robert B Nussenblatt; James T Rosenbaum
Journal:  Am J Ophthalmol       Date:  2005-09       Impact factor: 5.258

9.  The spectrum of Vogt-Koyanagi-Harada disease in Tunisia, North Africa.

Authors:  Moncef Khairallah; Sonia Zaouali; Riadh Messaoud; Sami Chaabane; Sonia Attia; Salim Ben Yahia; Kamel Hmidi
Journal:  Int Ophthalmol       Date:  2007-01-04       Impact factor: 2.029

10.  Vogt-Koyanagi-Harada disease in Hispanic patients.

Authors:  Somsiri Sukavatcharin; Julie H Tsai; Narsing A Rao
Journal:  Int Ophthalmol       Date:  2007-03-23       Impact factor: 2.029

View more
  1 in total

1.  "Revised diagnostic criteria" for Vogt-Koyanagi-Harada disease fail to improve disease management.

Authors:  Alireza Hedayatfar; Sana Khochtali; Moncef Khairallah; Masaru Takeuchi; Ahmed Abu El Asrar; Carl P Herbort
Journal:  J Curr Ophthalmol       Date:  2018-12-13
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.