Endothelial cell functions
- Maintain nonthrombotic interface – prostacyclin, thrombomodulin, heparin like, pasminogen ativator
- Store and release vWF, plasminogen activator inhibitor, tissue factor
- Maintain permeability – Controls trasfer of small and medium size molecules from blood stream to tissues.
- Modulate blood flow via vascular resistance
- Metabolism of hormones
- Regulation of immune and inflammatory reactions
- Growth regulation of smooth muscle cells.
- ECM production
- Oxidation of LDL
Arteriosclerosis:
- Definition – thickening or loss of elasticity in arterial walls
- Associated with diabetes and HTN
Atherosclerosis:
- Definition- intimal lesions called atheromas which protrude in vascular lumen.
- Risk factors.
- Non modifiable – age, male, family Hx, genetic abnormalities
- Modifiable – hyperlipidaemia, hypertension, diabetes, smoking
- Pathogenesis.
- Chronic endothelial injury –> accumulation of LDL in vessel wall–> modification of LDL by oxidation –> ahdesion and migration of monocytes–> adhesion of platelets–> release of factors from macrophages and platelets –> migration of SMCs from media to intima–> proliferation of SMCs–> elaboration of ECM–> accumulation of intracellular and extracellular lipids in the plaque.
- Clinically silent and from 1st decade: Isolated Foam cells –> fatty streaks–>
- From 3rd decade: Atheromas(now has core of extracellular fat)–>
- Lipid core + fibrotic layer or multiple, mainly calcific or fibrotic(accelerated smooth muscle and collagen increase): fibroatheromas–>
- Surface defect, haematoma, haemorrhage, thrombus: complicated lesions
- Mostly affects large elastic and large/medium muscular arteries.
- Stable plaque – has a dense collagenous and thick fibrous capsule with minimal inflammation and a small underlying atheromatous core
- Vulnerable plaque – thin fibrous cap, large lipid core and increased inflammation so it is prone to rupture.
- Pathological changes
- Rupture/fissuring – leads to exposure to highly thrombophilic lipid core
- Erosion/ulceration – exposing subendothelial basement membrane – also thrombophilic
- Haemorrhage into atheroma – expanding volume
- Clinical significance / complications.
- Consequences
- Small vessel occlusion- compromising distal perfusion
- Ruptured plaque–> can embolise or cause acute thrombus
- Destruction of vessel wall leading to aneurysm–> secondary rupture/thrombus
- Consequences
Hypertension:
- Causes / Pathogenesis.
- Genetic
- Familial multi gene foci interactions- vascular smooth muscle, Na metabolism,
- Environmental
- Stress
- Obesity
- Smoking
- High salt intake
- Physical inactivity
- Vasoconstrictive influences
- Primary HTN
- Genetic
- Consequences
- Atherosclerosis
- CAD, CVD, aortic dissection, renal failure, cardiac hypertrophy, CCF, retinal changes
- Malignant HTN – clinical syndrome of SBP>200, DBP>120, renal failure, encephalopathy, CVS abnormalities, rapidly rising BP, <5% of HTN patients, undtreated can cause death in 1-2yrs,
Aneurysms:
- Sites.
- Berry aneurysm in intersections of cerebral arteries.
- Abdominal
- Causes / Pathogenesis. – structure or function of the vascular wall connective tissue is compromised
- Poor intrinsic quality of the vascular wall connective tissue eg Marfans, Ehlers Danlos
- Collagen degradation vs synthesis by local inflammation inbalance – atherosclerosis, vasculitis
- Loss of vscular smooth muscle cells or inappropriate synthesis of noncollagenous or non elastic ECM(cystic medial degeneration) Grow at 0.2cm/yr
- Operative mortality 5% vs 50% if already ruptured.
- Complications.
- Rupture into peritoneum or retriperitoneum –> potentially lethal
- Obstruction of branching vessel–> ischaemic injury
- Embolisation – atheroma or mural thrombus
- Impingement of adjacent structures eg ureter
- Nothing esp if <4cm
- Risk of rupture
- 4cm or less = nil
- 4-5cm – low risk 1%
- 5cm-6cm 11%
- >6cm high risk 25% rupture per year
Aortic dissection.
- Defect in endothelial wall between intima and media and blood begins tracking down between the laminar planes of the media between middle and outer third.
- RFs – HYPERTENSION, collagen defects eg Elher’s Dhanlos, Marfans; iatrogenic during angiogram; age, pregnancy
- Pathogenesis – medial weakness due to underlying cause, medial hypertrophy of vaso varum, cystic medial degeneration.
- Cx – hypovolaemic shock, tamponade, MI, loss of end organ perfusion –> kidney failure etc, rupture and death.
- Split into Stanford
- type A (ascending aorta or both) and
- type B (descending aorta)
- De Bakey
- 1 – 60% involves ascending and descending
- II – 10-15% involves only ascending
- III – 25-30% involves only descending
Vasculitides:
- Direct infection – Neisseria, Rocky mountain spotted fever, aspergillosis
- Immunologic
- immune complex mediated
- Henoch Schonlein purpura, SLE, RA, cryoglobulinaemia, serum sickness
- ANCA mediated
- Wegners, microscopic polyangiitis, Churg-strauss
- Direct antibody mediated
- Good pasture(antiGBM), Kawasaki(antiendothelial Abs)
- Cell mediated
- Organ rejection
- Inflammatory bowel disease
- Paraneoplastic
- immune complex mediated
- Giant cell arteritis – large vessel
- Takayasu arteritis – large vessel
- Polyarteritis nodosa – medium vessel
Varicose veins:
- Abnormally dilated and tortuous veins produced by prolonged, increased intraluminal pressures and loss of vessel wall support
- Pathogenesis.
- Intraluminal thrombosis(DVT) or other valvular deformities –> venous pooling in superficial veins.
- Complications.
- Congestion, oedema, pain, thrombosis. Dermatitis, ulceration, prone to injury, poor healing
Vascular tumours
- Benign
- Haemangioma – present at births, grows but usually regresses by puberty.
- Lymphangioma
- Glomus tumour
- Vascular ectasis
- Intermediate neoplasm
- Karposi sarcoma – HHV 8
- Haemangioendothelioma
- Malignant
- Angiosarcoma
- Haemangiopericytoma