Literature DB >> 17437061

Vogt-Koyanagi-Harada disease in elderly Japanese patients.

Chihiro Kiyomoto1, Masamoto Imaizumi, Kenichi Kimoto, Hiromi Abe, Satoko Nakano, Kazuo Nakatsuka.   

Abstract

PURPOSE: The purpose of this study was to evaluate the characteristics of Vogt-Koyanagi-Harada (VKH) disease in elderly (age > or =65 years) Japanese patients.
METHODS: We reviewed the medical records of all patients diagnosed with VKH disease at the Department of Ophthalmology, Oita University Hospital between October 1982 and March 2005. Data extracted included age, gender, prodromal symptoms, visual acuity, ocular manifestations, extraocular findings, human leukocyte antigen (HLA), ocular complications, treatment, and smoldering inflammation.
RESULTS: Of the 68 patients with VKH disease, seven (10%) were classified as elderly at onset. The incidence of optic disk hyperemia, choroidal detachment, and cataract was significantly higher in the elderly patients than the non-elderly patients (<65 years). The total dose of corticosteroid used was higher in the elderly. The incidence of smoldering inflammation was more frequent in the elderly. Final visual acuity was preserved relatively well in the elderly.
CONCLUSION: The significantly higher incidence of optic disk hyperemia, choroidal detachment, and cataract, and the more frequent smoldering inflammation in elderly VKH patients indicate that special attention should be paid to these parameters in elderly patients.

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Year:  2007        PMID: 17437061     DOI: 10.1007/s10792-007-9067-4

Source DB:  PubMed          Journal:  Int Ophthalmol        ISSN: 0165-5701            Impact factor:   2.029


  13 in total

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  7 in total

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4.  Differences in the clinical features of two types of Vogt-Koyanagi-Harada disease: serous retinal detachment and optic disc swelling.

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5.  Neurosarcoidosis Occurring 6 Years after Onset of Vogt-Koyanagi-Harada Disease.

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Review 7.  Vogt-Koyanagi-Harada disease: review of a rare autoimmune disease targeting antigens of melanocytes.

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  7 in total

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