Behcet's disease Flashcards
(7 cards)
What is Behcet’s disease?
Inflammatory vasculitis affecting mucocutaneous, ophthalmological, vascular, GI and CNS systems, characterised by orogenital ulceration and uveitis.
What is the aetiology of Behcet’s disease?
Genetics: HLA-B51. Not associated with autoimmune of systemic inflammatory conditions.
What is the pathophysiology of Behcet’s disease?
Neutrophil hyper-reactivity
What is the epidemiology of Behcet’s disease: Gender? Where? Age?
More active and severe in males. Most common in Mediterranean, Middle East and far East. 20-40 years.
What are the signs and symptoms of Behcet’s disease? (x5)
- Oral and genital ulcers but only inside mouth. Never on lips like HSV. Genital ulcers are painful and often infected, particularly found on scrotum
- Uveitis
- Acne lesions in atypical locations such as arms and legs
- Erythema multiforme
- Neurological: memory loss, meningeal inflammation
- Crampy abdominal pain, diarrhoea and GI ulceration
What is the disease progression of Behcet’s disease?
Becomes less severe with time
What are the investigations for Behcet’s disease? (x4)
- PATHERGY TESTING: subcutaneous needle-prick becomes inflamed and a sterile pustule develops within 24-48 hours
- LP when neurological involvement suspected
- Colonoscopy when GI involvement to rule out other pathologies
- RF, ANA, ANCA to exclude other pathologies