Journals / Güncel Retina Dergisi / 2018 / Cilt: 2 - Sayı: 4

Clinical Findings, Diagnosis and Classification of Behçet’s Disease

Behçet Hastalığı’nda Klinik Bulgular, Klinik Tanı ve Sınıflandırma

Pages
329–333
DOI
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AI Summary & Key Takeaways

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

This article aims to review the clinical findings, diagnosis and classification of BD.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Behçet’s Disease (BD) is a chronic multisystem vasculitis with unknown etiology, which is characterized with the triad of recurrent oral ulcers, genital ulcers, and iritis.
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Key Findings & Data:Eye is one of the most commonly affected organs and typical ocular involvement is panuveitis with hypopyon and retinal vasculitis.
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Conclusion & Impact:This article aims to review the clinical findings, diagnosis and classification of BD.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Behçet’s Disease (BD) is a chronic multisystem vasculitis with unknown etiology, which is characterized with the triad of recurrent oral ulcers, genital ulcers, and iritis. Eye is one of the most commonly affected organs and typical ocular involvement is panuveitis with hypopyon and retinal vasculitis. The diagnosis is based on clinical evaluation including biomicroscopic and funduscopic examination. This article aims to review the clinical findings, diagnosis and classification of BD.

Özet

Behçet Hastalığı (BH) tekrarlayan oral ülser, genital ülser ve iritis triadı ile karakterize etiyolojisi bilinmeyen kronik multisistemik bir vaskülittir. Göz en sık etkilenen organlar arasında yer alır ve tipik oküler tutulum hipopyonlu panüveit ve retinal vaskülit şeklinde olmaktadır. Tanı biyomikroskopik ve funduskopik muayeneyi içeren klinik değerlendirmeye dayanmaktadır. Bu makalede BH’nın klinik bulguları, tanı ve sınıflamasının gözden geçirilmesi amaçlanmıştır.

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Cite This Article

YILMAZ, S. G., YÜCE, B., ATEŞ, H. (2018). Clinical Findings, Diagnosis and Classification of Behçet’s Disease. Güncel Retina Dergisi, Cilt: 2 - Sayı: 4, 329–333. https://ajindex.com/articles/190651

References (13)

  1. Nussenblatt RB. Behçet’s Disease. In: Nussenblatt RB and Whitcup SM (eds), Uveitis: Fundamentals and Clinical Practice 4th Edition,
  2. St. Louis, Mosby, 2010;332- 54. Behçet H. Uber rezideivierende, aphthose durch ein virus verursachte Geschwüre am Mund, am Auge und an den Genitalien. Dermatol Wochenschr 1937;46:414-19.
  3. Lehner T, Batchelor JR, Challacombe SJ, Kennedy L. An immunogenetic basis for the tissue involvement in Behçet’s syndrome. Immunology 1979;37(4):895-900.
  4. Idil A, Gürler A, Boyvat A, Caliskan D, Ozdemir O, Isik A, et al. The prevalence of Behçet’s disease above the age of 10 years. The results of a pilot study conducted at the Park Primary Health Care Center in Ankara, Turkey. Ophthalmic Epidemiol. 2002;9(5):325-31.
  5. Azizlerli G, Köse AA, Sarica R, Gül A, Tutkun IT, Kulaç M, et al. Prevalence of Behçet’s disease in Istanbul, Turkey. Int J Dermatol. 2003;42(10):803-6.
  6. Kazokoglu H, Onal S, Tugal-Tutkun I, Mirza E, Akova Y, Ozyazgan Y, et al. Demographic and clinical features of uveitis in tertiary centers in Turkey. Ophthalmic Epidemiol. 2008;15(5):285-93.
  7. Yalçındağ FN, Özdal PC, Özyazgan Y, Batıoğlu F, Tugal-Tutkun I; BUST Study Group. Demographic and Clinical Characteristics of Uveitis in Turkey: The First National Registry Report. Ocul Immunol Inflamm.2016:1-10. doi: 10.1080/09273948.2016.1196714. [Epub ahead of print] Ustun C. A famous Turkish dermatologist, Dr. Hulusi Behçet. Eur J Dermatol. 2002;12(5):469-70.
  8. Atmaca LS, İdil A, Batıoğlu F. A descriptive study on Behçet’s disease. Acta Ophthalmol Scand 1996;74(4):403-6.
  9. Davatchi F, Shahram F, Chams-Davatchi C, Shams H, Nadji A, Akhlaghi M, et al. Behcet’s disease: from east to west. Clin Rheumatol. 2010;29(8):823–33.
  10. Atmaca LS, Atmaca Sönmez P. Behçet Hastalığında Göz Tutulumu. Retina-Vitreus 2004;12(Sp): 77-86. Şengün A. Behçet Hastalığı. IN: Akbatur HH, Şengün A (eds). Behçet Hastalığı, Endoftalmiler ve Üveitler. Atlas Kitapçılık Tic.Ltd.Şti, Ankara, 2002;79-105.
  11. Doğanavşargil E, Keser G, Behçet hastalığı. In: Gümüşdiş G, Doğanavşargil E, (eds). Klinik Romatoloji, 1. Baskı.
  12. İstanbul, Deniz matbaası, 1999;423-39. Barnes CG. Behçet’s syndrome-classification criteria. Ann Med Interne 1999;150(6):447-82. International Study Group for Behcet’s Disease. Criteria for diagnosis of Behcet’s syndrome. Lancet 1990;335(8697):1078-80.
  13. Tugal-Tutkun I, Onal S, Altan-Yaycioglu R, Huseyin Altunbas H, Urgancioglu M. Uveitis in Behçet disease: an analysis of 880 patients. Am J Ophthalmol. 2004;138(3):373-80.