Behcet's syndrome
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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."[1]
A variation may be Hughes-Stovin Syndrome which is pulmonary artery aneurysms associated with systemic thrombosis.[2][3]
References
- ↑ Anonymous (2024), Behcet's syndrome (English). Medical Subject Headings. U.S. National Library of Medicine.
- ↑ 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.
- ↑ 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.