Difference between revisions of "Behçet's syndrome"
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==Microscopic== | ==Microscopic== | ||
Features - vasculitis:<ref name=pmid22100288/> | Features - small vessel [[vasculitis]]:<ref name=pmid22100288/><ref name=pmid17207160>{{Cite journal | last1 = Kalayciyan | first1 = A. | last2 = Zouboulis | first2 = C. | title = An update on Behçet's disease. | journal = J Eur Acad Dermatol Venereol | volume = 21 | issue = 1 | pages = 1-10 | month = Jan | year = 2007 | doi = 10.1111/j.1468-3083.2006.01863.x | PMID = 17207160 }}</ref> | ||
*[[Fibrinoid necrosis]] of the vessel walls. | *[[Fibrinoid necrosis]] of the vessel walls. | ||
*Inflammatory cells in the blood vessel walls. | *Inflammatory cells in the blood vessel walls. | ||
Revision as of 23:08, 1 June 2012
Behçet's syndrome, also Behçet's disease, is a rare disorder classically described as the triad of:[1]
- Oral aphthous ulcers.
- Genital ulcers.
- Uveitis
General
Etiology:
- Unknown - hypothesized to be infectious due to the epidemiology.[2]
Clinical
Microscopic
Features - small vessel vasculitis:[2][3]
- Fibrinoid necrosis of the vessel walls.
- Inflammatory cells in the blood vessel walls.
References
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) 109650
- ↑ 2.0 2.1 2.2 Hatemi, G.; Yazici, H. (Jun 2011). "Behçet's syndrome and micro-organisms.". Best Pract Res Clin Rheumatol 25 (3): 389-406. doi:10.1016/j.berh.2011.05.002. PMID 22100288.
- ↑ Kalayciyan, A.; Zouboulis, C. (Jan 2007). "An update on Behçet's disease.". J Eur Acad Dermatol Venereol 21 (1): 1-10. doi:10.1111/j.1468-3083.2006.01863.x. PMID 17207160.