Journals / Bozok Tıp Dergisi / 2014 / Cilt: 4 - Sayı: 2

Mucocutaneous Manifestations of Behcet s Disease

BEHÇET HASTALIĞINDA DERİ VE MUKOZA BELİRTİLERİ

Pages
53–58
Publication Date
2022-10-11
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

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

In this review, mucocutaneous symptoms of Behcet s disease are outlined.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Behcet s disease is a multi-system inflammatory disorder of unknown origin, characteri- zed by recurrent oral and genital ulcerations, ocular and cutaneous lesions, arthritis and vascular disease.
📊
Key Findings & Data:Various mucocutaneous manifestations consisting mainly of recurrent oral and genital ulcerations, erythema nodosum like lesions and papulopustular lesios constitute the hallmark of Behcet s disease and diagnostic criteria rely heavily on these symptoms.
💡
Conclusion & Impact:In this review, mucocutaneous symptoms of Behcet s disease are outlined.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Behcet s disease is a multi-system inflammatory disorder of unknown origin, characteri- zed by recurrent oral and genital ulcerations, ocular and cutaneous lesions, arthritis and vascular disease. Various mucocutaneous manifestations consisting mainly of recurrent oral and genital ulcerations, erythema nodosum like lesions and papulopustular lesios constitute the hallmark of Behcet s disease and diagnostic criteria rely heavily on these symptoms. In addition, although the mucocutaneous manifestations are not one of the main prognostic determinants in Behcet s disease, they seem to impair the quality of life of the patients. In this review, mucocutaneous symptoms of Behcet s disease are outlined.

Özet

Behçet hastalığı rekürren oral ve genital ülserler, oküler ve kutanöz lezyonlar, artrit ve vasküler tutulum ile karakterize kesin nedeni bilinmeyen multisistem inflamatuar bir hastalıktır. Tekrarlayıcı nitelikteki oral ve genital ülserler, eritema nodozum benzeri lez- yonlar ve papülopüstüler lezyonlar başta olmak üzere çeşitli deri ve mukoza bulguları gösteren hastalığın tanısında da bu bulguların kritik önemi bulunmaktadır. Ayrıca, Behçet hastalığındaki mukokutanöz bulguların diğer ciddi organ tutulumlarına göre prognostik belirleyici özellikleri olmamasına karşın, hastaların yaşam kalitesini etkiledikleri açıktır. Bu derlemede Behçet hastalığının deri ve mukoza belirtileri anlatılmaktadır.

🔖

Cite This Article

ÇÖLGEÇEN, E., ÖZYURT, K., BORLU, M. (2022). Mucocutaneous Manifestations of Behcet s Disease. Bozok Tıp Dergisi, Cilt: 4 - Sayı: 2, 53–58. https://ajindex.com/articles/468975

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (17)

  1. Behçet H. Uber rezidivierende, aphthose, dürch ein Virus verursachte Geshwure am Munde, am Auge und an den Genitalien. Dermatologische Wochenschrift. 1937;36(1):1152-7
  2. Alpsoy E. Behçet hastalığının deri ve mukoza belirtileri. Türkderm. 2003;37(2):92-9
  3. Onder M, Gürer MA. The multiple faces of Behçet’s disease and its aetiological factors. J Eur Acad Dermatol Venereol. 2001;15(2):126-36
  4. Bang D. Clinical spectrum of Behçet’s disease. J Dermatol. 2001;28(11):610-3
  5. Lee LA. Behçet disease. Semin Cutan Med Surg. 2001;20(1):53-7
  6. Saylan T, Mat C, Fresko I, Melikoğlu M. Behçet’s disease in the Middle East. Clin Dermatol. 1999;17(2):209-23
  7. Sakane T, Takeno M, Suzuki N, Inaba G. Behçet’s disease. N Engl J Med. 1999;341(17):1284-91
  8. Hedayatfar A. Behçet’s Disease: Autoimmune or autoinflammatory? J Ophthalmic Vis Res. 2013;8(3):291-3
  9. Muşabak U. Otoinflamatuar bir hastalık olarak Behçet hastalığı. Turkiye Klinikleri J Dermatol-Special Topics. 2011;4(4):32-44
  10. International Study Group for Behçet’s Disease. Criteria for diagnosis of Behçet’s disease. Lancet. 1990;335(8697):1078-80
  11. Alpsoy E, Donmez L, Bacanli A, Apaydin C, Butun B. Review of the chronology of clinical manifestations in 60 patients with Behçet’s disease. Dermatology. 2003;207(4):354-6
  12. Önder M, Gürer MA. Ülkemizde Behçet hastalığı epidemiyolojisi. Turkiye Klinikleri J Int Med Sci. 2007;3(9):4-7
  13. Demirhindi O, Yazıcı H, Binyıldız P, Dayıoğlu N, Tüzün Y, Altaç M, et al. Silivri Fener Köyü ve yöresinde Behçet Hastalığı sıklığı ve bu hastalığın toplum içinde taranmasında kullanılabilecek bir yöntem. Cerrahpaşa Tıp Fak Derg. 1981;12(1):509-14
  14. Yurdakul S, Günaydın İ, Tüzün Y, Tankurt N, Pazarlı H, Özyazgan Y, et al. The prevalence of Behcet’s syndrome in a rural area in northern Turkey. The Journal of Rheumatology. 1988;15(5):820-2
  15. 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 Epidemiology. 2002;9(5):325-31
  16. Azizlerli G, Köse AA, Sarica R, Gül A, Tutkun IT, Kulaç M, et al. Prevalence of Behçet’s disease in Istanbul, Turkey. International Journal of Dermatology. 2003;42(10):803-6
  17. Cakir N, Dervis E, Benian O, Pamuk ON, Sonmezates N, Rahimoglu R, et al. Prevalence of Behçet’s disease in rural western Turkey: a preliminary report. Clinical and Experimental Rheum