Behcet's syndrome: Difference between revisions

From Citizendium
Jump to navigation Jump to search
imported>Howard C. Berkowitz
No edit summary
imported>Stefan Olejniczak
No edit summary
Line 1: Line 1:
{{subpages}}
{{subpages}}
In [[rheumatology]], '''Behcet's Syndrome''', or '''Behçet's Disease''', is a "rare chronic inflammatory disease involving the small blood vessels. It is of unknown etiology and characterized by mucocutaneous ulceration in the mouth and genital region and [[uveitis]] with hypopyon. The neuro-ocular form may cause blindness and death. [[Synovitis]]; [[thrombophlebitis]]; gastrointestinal ulcerations; [[retinal vasculitis]]; and [[optic atrophy]] may occur as well."<ref>{{MeSH}}</ref>  
In [[rheumatology]], '''Behcet's Syndrome''', or '''Behçet's Disease''', is a rare chronic inflammatory disease involving the small blood vessels. It is of unknown etiology and characterized by mucocutaneous ulceration in the mouth and genital region, and [[uveitis]] with hypopyon. Other symptoms are painful, stiff and swollen joints <ref>http://www.nlm.nih.gov/medlineplus/behcetssyndrome.html</ref>. The neuro-ocular form may cause blindness and death. [[Synovitis]]; [[thrombophlebitis]]; gastrointestinal ulcerations; [[retinal vasculitis]]; and [[optic atrophy]] may occur as well."<ref>{{MeSH}}</ref>  


A variation may be Hughes-Stovin Syndrome which is pulmonary artery aneurysms associated with systemic [[thrombosis]].<ref name="pmid17457658">{{cite journal| author=Emad Y, Ragab Y, Shawki Ael-H, Gheita T, El-Marakbi A, Salama MH| title=Hughes-Stovin syndrome: is it incomplete Behçet's? Report of two cases and review of the literature. | journal=Clin Rheumatol | year= 2007 | volume= 26 | issue= 11 | pages= 1993-6 | pmid=17457658  
A variation may be Hughes-Stovin Syndrome which is pulmonary artery aneurysms associated with systemic [[thrombosis]].<ref name="pmid17457658">{{cite journal| author=Emad Y, Ragab Y, Shawki Ael-H, Gheita T, El-Marakbi A, Salama MH| title=Hughes-Stovin syndrome: is it incomplete Behçet's? Report of two cases and review of the literature. | journal=Clin Rheumatol | year= 2007 | volume= 26 | issue= 11 | pages= 1993-6 | pmid=17457658  

Revision as of 15:39, 18 August 2010

This article is developing and not approved.
Main Article
Discussion
Definition [?]
Related Articles  [?]
Bibliography  [?]
External Links  [?]
Citable Version  [?]
 
This editable Main Article is under development and subject to a disclaimer.

In rheumatology, Behcet's Syndrome, or Behçet's Disease, is a rare chronic inflammatory disease involving the small blood vessels. It is of unknown etiology and characterized by mucocutaneous ulceration in the mouth and genital region, and uveitis with hypopyon. Other symptoms are painful, stiff and swollen joints [1]. The neuro-ocular form may cause blindness and death. Synovitis; thrombophlebitis; gastrointestinal ulcerations; retinal vasculitis; and optic atrophy may occur as well."[2]

A variation may be Hughes-Stovin Syndrome which is pulmonary artery aneurysms associated with systemic thrombosis.[3][4]

Notable cases

Hughes-Stovin Syndrome was diagnosed in the "The Down Low" in season 6, episode 10 of the television series House.

References

  1. http://www.nlm.nih.gov/medlineplus/behcetssyndrome.html
  2. Anonymous (2024), Behcet's syndrome (English). Medical Subject Headings. U.S. National Library of Medicine.
  3. Emad Y, Ragab Y, Shawki Ael-H, Gheita T, El-Marakbi A, Salama MH (2007). "Hughes-Stovin syndrome: is it incomplete Behçet's? Report of two cases and review of the literature.". Clin Rheumatol 26 (11): 1993-6. DOI:10.1007/s10067-007-0609-y. PMID 17457658. Research Blogging.
  4. Erkan D, Yazici Y, Sanders A, Trost D, Yazici H (2004 Jul-Aug). "Is Hughes-Stovin syndrome Behçet's disease?". Clin Exp Rheumatol 22 (4 Suppl 34): S64-8. PMID 15515789.