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Journals / Retina-Vitreus / 2007 / Cilt: 15 - Sayı: 2

Vogt Koyanagi Harada Syndrome: Report of Two Cases

Vogt Koyanagi Harada Sendromu: İki Olgunun Sunumu

M.Ertoğrul MİRZA
Ayşe ÖNER
Sarper KARAKÜÇÜK
Türkan PITIROĞLU
HATİCE ARDA
Pages
137–140
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In this paper, we presented two cases of VKH syndrome with different clinical findings7

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Vogt Koyanagi Harada (VKH) Syndrome is an idiopatic, multisystem disorder.
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Key Findings & Data:Skin and hair disorders include alopecia, poliosis, and vitiligo.
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Conclusion & Impact:In this paper, we presented two cases of VKH syndrome with different clinical findings7
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Vogt Koyanagi Harada (VKH) Syndrome is an idiopatic, multisystem disorder. Skin and hair disorders include alopecia, poliosis, and vitiligo. Neurological features include headache, encephalopathy, auditory symptoms and lmphocytosis in cerebrospinal fluid. Chronic granulomatous iridocyclitis, optic disc hyperaemia or oedema and multifocal detachments of the sensory retina at the posterior pole are the features of the ocular involvement. In this paper, we presented two cases of VKH syndrome with different clinical findings7

Özet

-------------------------------------------------------------------------------- Vogt-Koyanagi-Harada (VKH) idiopatik, birden fazla sistemi ilgilendiren bir hastalıktır. Cilt ve saç bulguları alopesi, poliozis ve vitiligo şeklindedir. Nörolojik bulgular başağrısı, ensefalopati, işitme sistemine ait bulgular ve BOS’ta lenfositozu içerir. Oküler tutulum bulguları ise kronik granülomatöz iridosiklit, optik disk hiperemisi veya ödemi, arka kutupta multifokal sensoryel retina dekolmanları şeklindedir. Bu yazıda değişik klinik bulgularla başvuran iki VKH sendromlu olgu sunulmuştur

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Cite This Article

MİRZA, M., ÖNER, A., KARAKÜÇÜK, S., PITIROĞLU, T., ARDA, H. (2007). Vogt Koyanagi Harada Syndrome: Report of Two Cases. Retina-Vitreus, Cilt: 15 - Sayı: 2, 137–140. https://ajindex.com/articles/305261

References (7)

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  2. Moorthy RS, Inomata H, Rao NA.: Vogt-Koyanagi-Harada syndrome. Surv Ophthalmol. 1995;39:265-292
  3. Read RW, Rao NA, Cunningham ET.: Vogt-Koyanagi-Harada disease. Curr Opin Ophthalmol. 2000;11:437-442
  4. Read RW, Holland GN, Rao NA, et al.: Revised diagnostic criteria for Vogt-Koyanagi-Harada disease: report of an international committee on nomenclature. Am J Ophthalmol. 2001;131:647-652
  5. Read RW, Rechodouni A, Butani N, et al.: Complications and prognostic factors in Vogt-Koyanagi-Harada disease. Am J Ophthalmol. 2001;131:599-606
  6. Kotake S, Ohno S.: 'Pulse' methylprednisolone therapy in the treatment of Vogt-Koyanagi-Harada's disease. Jap J Clin Opthalmol. 1984;38:1053-1058
  7. Yamanaka E, Ohguro N, Yamamoto S, et al.: Evaluation of Pulse Corticosteroid Therapy for Vogt-Koyanagi-Harada Disease Assessed by Optical Coherence Tomography. Am J Ophthalmol. 2002;134:454-456.