Blood Vessel Diseases Flashcards
Vascular inflammatory injury, with necrosis of blood vessels
vasculitides
What type of vessels are affected in vasculitides?
any size or location
Clinical manifestations of vasculitis depends on what?
level of ischemia caused by vasculitis
Causes of vasculitides are unknown, but may include:
1) reaction to immune-complex deposition (type III hypersensitivity)
2) cell-mediated immunity mechanism
Large vessel vasculitis
Temporal Arteritis
Takayasu Arteritis
- occurs in >50 (esp of Nordin origin)
- arteries of the head (esp temporal and vertebral aa)
- nodular thickenings of vessel with reduction of lumen
- granulomatous inflammation (MHC-Class II)
- T-cell mediated
Temporal Arteritis (Giant cell) - macrophages form multi-nucleated giant cell, not granulomas
Symptoms of temporal arteritis
- vague, sometimes fever, fatigue, weight loss
- headache (along superficial temporal a), sometimes pain on palpation, facial pain
- vision problems if ophthalmic a is involved
Granulomatous vasculitis of medium and large arteries (esp aortic arch and branches) also pulmonary (50%), coronary and renal arteries
- inflammation causes intimal thickening
- giant cell inflammation
Takayasu Arteritis “Pulseless disease”
- Characterized by ocular disturbances and weakening of pulses in upper extremities
- Predominantly females under 40
Takayasu Arteritis
Arteries mostly affected by Takayasu Arteritis
Aortic branch and pulmonary a
Type III immune injury involving immune complexes (associated with Hep B and C)
polyarteritis nodosa
characterized by necrotizing immune complex inflammation of small and medium sized arteries
polyarteritis nodosa
Disease usually of young adults
Malaise, fever, weight loss, hypertension, abdominal pain and melena, myalgia, ulcers, infarcts, peripheral neuritis
polyarteritis nodosa
- Renal arterial involvement often prominent and major cause of death
- 30% of patients with this disease have Hep B surface Ag/Ab complexes
polyarteritis nodosa
Treatment for polyarteritis nodosa
steroids and cyclophosphamide
Histological findings include presence of fibrinoid necrotizing vasculitis of medium and small arteries (neutrophils)
polyarteritis nodosa
Angiographic findings include aneurysms or occlusions of the visceral arteries (looks beaded)
polyarteritis nodosa
- Often affect Asian infants (
Kawasaki disease
Kawasaki disease is aka
mucocutaneous lymph node syndrome
Coronary a aneurysm
Kawasaki disease
Diagnosis criteria for Kawasaki disease (mnemonic: CREAM)
4 ouf of 5: Conjunctivitis Rash Edema Adenopathy Mucosal involvement
Triad of:
1) necrotizing granulomas of upper respiratory tract
2) granulomatous vasculitis of medium and small vessels
3) necrotizing, often crescentic glomerulonephritis
- lungs and kidneys
granulomatosis with polyangitis (Wegener)
Possible over reaction to allergens
Granulomatosis with Polyangitis (Wegener)
Predominately signs and symptoms of respiratory tract, esp of paranasal sinuses and lungs, and necrotizing glomerulonephritis
Granulomatosis with Polyangitis (Wegener)