Clinical observation of Behçet's disease in a 33-year-old woman
- Authors: Zhulimova NL1, Zil'berberg NV1, Levchik NK1
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Affiliations:
- ФГБУ "Уральский научно-исследовательский институт дерматовенерологии и иммунопатологии" Минздрава России, Екатеринбург, Россия
- Issue: Vol 86, No 12-2 (2014)
- Pages: 43-46
- Section: Editorial
- URL: https://journals.rcsi.science/0040-3660/article/view/31618
- ID: 31618
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Abstract
The paper describes a clinical case of Behçet's disease accompanied by oral aphthous elements and external genital sores. The disease occurred after an infectious and inflammatory process in the oropharynx; chronic erythema nodosum and arthritides were successively diagnosed. A set of anamnestic data and clinical and laboratory examinations could establish a correct diagnosis.
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##article.viewOnOriginalSite##About the authors
N L Zhulimova
ФГБУ "Уральский научно-исследовательский институт дерматовенерологии и иммунопатологии" Минздрава России, Екатеринбург, Россия
Email: nat73zh@gmail.com
N V Zil'berberg
ФГБУ "Уральский научно-исследовательский институт дерматовенерологии и иммунопатологии" Минздрава России, Екатеринбург, Россия
N K Levchik
ФГБУ "Уральский научно-исследовательский институт дерматовенерологии и иммунопатологии" Минздрава России, Екатеринбург, Россия
References
- Hatemi G., Yazici Y., Yazici H. Behcet's syndrome. Rheum Dis Сlin North Am. 2013 May; 39 (2): 245-61. doi: 10.1016/j.rdc.2013.02.010/ Epub 2013 Mar 14.
- Pohl D., Benseler S. Systemic inflammatory and autoimmune disorders. Handb Clin Neurol 2013; 112: 1243-1252.
- Al-Araji A., Kidd D.P. Neuro-Behcet's diseases: epidemiology, clinical characteristics, and management. Lancet Neurol 2009; 8 (2): 192-204.
- Измайлова Ф.И., Алекберова З.С. Болезнь Бехчета: демографические и генетические аспекты (Обзор литературы). Современная ревматология. 2014; 1: 53-58.
- Алекберова З.С. Болезнь Бехчета. Москва: РАМН и ГУ РАМН; 2007.
- Алекберова З.С., Измаилова Ф.И., Кудаев М.Т. Болезнь Бехчета: клинико-демографические ассоциации. Терапевтический архив 2013; 85 (5): 48-52.
- Yazici Y., Yurdakul S., Yazici H. Behcet's syndrome. Curr Rheumatol rep. 2010 Dec; 12 (6): 429-35. doi: 10.1007/11926-010-0132-z.
- Ohno S., Aoki K., Sugiura S. et al. Immunohematological studies on Behcet's disease. Histocompatibility (HL-A) antigens and I blood group system (author's transl.). Nicon Ganka Gakkai Zasshi. 1973; 77 (9): 1452-1458.
- Tappuni A.R., Tbakhi A., Sharguite K.E. et al. A comparative study of the genetics of Behcetçs disease in Iraq: international collaboration to transfer clinical and laboratory skills to Baghdad medical school and hospitals. Med Confl Survive 2013; 29 (1): 57-68.
- Guarene M., Capittini C., De Silvestri A. et al. Targeting the immunogenetic diseases with the appropriate HLA molecular typing: critical appraisal on 2666 patients typed in one single centre. Biomed Res Int. 2013; 2013:904247. doi: 10.1155/2013/904247. Epub 2013 Jan 21.
- Hughes T., Coit P., Adler A. et al. Identification of multiple independent susceptibility loci in the HLA region in Behçet's disease. Nat Genet 2013; 45 (3): 319-324.
- Kalayciyan A., Zouboulis C.C. An update on Behcet's disease. J Eur Acad Dermatol Venereol 2007; 21 (1): 1-10.
- Yanagihori H., Oyama N., Nakamura K. et al. Role of IL-12B promoter polymorphism in Adamantiades-Behcet's disease susceptibility: An involvement of Th1 immunoreactivity against Streptococcus sanguinis antigen. J Invest Dermatol 2006; 126 (7): 1534-1540.
- Cho S., Zheng Z., Cho S. et al. Both the sera of patients with Behçet's disease and Streptococcus sanguis stimulate membrane expression of hnRNP A2/B1 in endothelial cells. Scand J Rheumatol 2013; 42 (3): 241-246.
- Miyake S. Innate immunity in neuroimmunlogical disorders. Nihon Rinsho 2013; 71 (5): 778-782.
- Hamzaoui K., Kahon A., Hanza M., Ayed K. Supressive T cell function of Epstein-Barr virus induced B cell activation in active Behçet's disease. Clin Exp Rheumatol 1991; 9 (2): 131-135.
- Lee S.H., Kim S.D., Kim S.H. et al. EBV-associated haemophagocytic syndrome in a patient with Behçet's disease. Scand J Rheumatol 2005; 34 (4): 320-323.
- Kuhara T., Watanabe D., Ishida N. et al. Quantitative analysis of shedding of Epstein-Barr virus in saliva from patients with connective tissue disease: a pilot study. Int J Dermatol 2013; 52 (7): 887-890.
- Жулимова Н.Л., Бочкарев Ю.М., Чигвинцева Е.А., Сурганова В.И. Острая язва вульвы. Клин дерматол и венерол 2006; 1: 33-35.
- Hatemi G., Yazuci H. Behçet's syndrome and micro-organisms. Best Pract Res Clin Rheumatol. 2011; 25 (3): 389-406.
- Вольф К., Голдсмит Л.А., Кац С.И. и др. Дерматология Фицпатрика в клинической практике: в 3 т.: (пер. с англ.) М.: Изд-во Панфилова; 2012.
- Hatemi G., Silman A., Bang D. et al. EULAR recommendations for the management of Behçet disease. Ann Rheum Dis 2008; 67 (12): 1656-1662.
- The International Criteria for Behçet's Disease (ICBD): a collaborative study of 27 countries on the sensitivity and specificity of the new criteria. JEADV 2014; 28: 338-347.