Diseases of the Thoracic Aorta Flashcards

1
Q

What are the three layers of the aorta?

A

Tunica intima, tunica media, tunica adventitia.

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2
Q

What is the tunica intima composed of?

A

Endothelial cells, sub endothelial layer - collagen and elastin fibres. Separated from tunica media internal elastic membrane.

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3
Q

What is the tunica media composed of?

A

Smooth muscle cells which secrete elastin in the form of sheets or lamellae.

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4
Q

What is the tunica adventitia composed of?

A

Thin connective tissue layer. Collagen fibres and elastin fibres (not llamellae). The collagen in the adventitia prevents elastic arteries from stretching beyond their physiological limits during systole.

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5
Q

When will atherosclerosis start?

A

Can begin in early childhood.

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6
Q

What are the risk factors for atherosclerosis?

A

Hypertension, hypercholesterolaemia, smoking, diabetes, family history, male (relative protection in females until menopause).

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7
Q

What are some things atherosclerosis in the aorta can cause?

A

Stroke, MI, aneurysm

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8
Q

What is an aneurysm?

A

A localised enlargement of an artery caused by weakening of the vessel wall.

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9
Q

What is a true aneurysm?

A

Cause by weakness and dilation of all three layers of the wall. It is associated with hypertension, atherosclerosis, smoking and collagen abnormalities (Marfans, cystic medial necrosis), trauma, infection (mycotic/syphillis).

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10
Q

What is a false aneurysm?

A

Rupture of the wall of aorta with the haematoma wither contained by the thin adventitial layer or by the surrounding soft tissue ???

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11
Q

What is an aortic dissection?

A

Tear in inner wall of aorta, blood forces walls apart. Can be acute - medical/surgical emergency or chronic (smaller, healing themselves).

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12
Q

Why is an arch aneurysm really dangerous?

A

Thats where the branches come off.

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13
Q

What are some different types of aortic aneurysm (classified by site)?

A

Ascending aorta aneurysm, aortic arch aneurysm, descending aorta aneurysm, abdominal aorta aneurysm.

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14
Q

What are some signs and symptoms of thoracic aneurysms?

A

Asymptomatic or
based on location of aneurysm - SoB or even heart failure (AR), dysphagia and hoarseness (ascending aorta, chronic), sharp chest pain radiating to back (b/w shoulder blades) - possible dissection, pulsatile mass, hypotension.

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15
Q

What aetiological factors may contribute to aorta dissection?

A

Hypertension, athersclerosis, trauma, Marfans.

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16
Q

Histologically what would an aortic dissection look like?

A

Cystic medial necrosis, false lumen can progress in an antegrade (down into the distal aorta) or retrograde (back into the ascending aorta).
May occlude branches (e.g. mesenteric, carotid, renal and spinal).

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17
Q

What are the two classifications of aortic dissections?

A

Stanford and DeBakey.

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18
Q

Describe Stanford classification.

A

Type A - all dissections involving the ascending aorta, regardless of the site of origin.
Type B - all dissections not involving the ascending aorta.

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19
Q

Describe the DeBakey classification?

A

Stpe I - originates in the ascending aorta, propagares at least ti the aortic arch and often beyond it distally.
Type II - originates in t

20
Q

How might people present with an aortic dissection by showing neurological symptoms?

A

Dissection has caused occlusion of the carotid.

21
Q

How might an aortic dissection rupture?

A

Back into the lumen or externally into the pericardium (tamponade) or mediastinum.

22
Q

What might dilation of ascending aorta cause?

A

Patients may present in acute heart failure, if tear in heart valves causing acute aortic regurgitation.

23
Q

What are the symptoms of aortic dissection?

A

Tearing, severe chest pain (radiating to back)
Collapse (tamponade, acute AR, external rupture)
Beware inferior ST elevation
(50% mortality pre-hospital).

24
Q

What signs might you find on examination of aortic dissection?

A

Reduced or absent peripheral pulses (BP mismatch between sides)
Hypotension/hypertension
Soft early diastolic murmur (AR)
Pulmonary oedema
CXR usually shows widened mediastinum
Diagnosis can be confirmed by echocardiogram or CT.

25
Q

How do you treat type A (ascending aorta) aortic dissection?

A

Surgery.

26
Q

How do you treat type B (descending aorta) aortic dissection?

A

Meticulous BP control.
Sodium nitroprusside plus beta blocker.
Might also use GTN with an aim to keep BP stable.
Can be treated without surgery.

If impaired renal function, may give EVAR.

27
Q

What might cause inflammation of the thoracic aorta?

A

Takayasu’s Artertitis.

28
Q

What might cause infection of the thoracic aorta?

A

Syphyllis.

29
Q

What is Takayasu’s Arteritis? And how is it treated?

A
Rare. 
Granulomatous vasculitis. 
Females>males. 
Aorta and main branches. 
Stenosis, thrombosis, aneurysms, renal artery stenosis, neurological sx. 
Treated with steroids and surgery.
30
Q

What is syphilis caused by?

A

STD - treponema pallidum.

Antibiotics prevent late stages.

31
Q

How does syphilis present?

A

Primary - chancre, secondary - massive sores.

Tertiary - without treatment 1/3rd develop 1 of 3 types - late neuro-syphilis, gummatous syphilis, cardiac syphilis (10-30yrs post infection).

32
Q

What can cardiac syphilis cause?

A

Syphilitic aortitis - aneurysm.

Aortic regurgitation.

33
Q

What might congenital conditions might cause an aortic aneurysm?

A

Bicuspid aortic valve, Marfans, coarctation.

34
Q

What is the most common congenital abnormality?

A

Bicuspid aortic valve. 1-2% prevalence.

35
Q

What are people with bicuspid aortic valves prone to?

A

Prone to stenosis with or without regurgitation. Associated with coarctation. Abnormal aorta (reduced tensile strength), prone to aneurysm/dissection.

36
Q

How would you monitor someone with bicuspid aortic valve?

A

Monitor with echo/MRI.

37
Q

What is aortic coarctation?

A

Aortic narrowing normally close to where the ductus arterioles inserts (ligament arteriosum).

38
Q

What are the three types of coarctation?

A

Pre-ductal (5% turner’s) can be life threatening if severe narrowing.
Ductal
Post-ductal - most common in adults - hypertension in upper extremities, weak pulses in lower limbs.

39
Q

What are the signs of coarctation?

A

Cold legs, poor leg pulses, if before left subclavian artery (radial - radial and right radial femoral delay).
If after left subclavian artery - no radial/radial delay, right and left radio-femoral delay.

40
Q

What are the symptoms of coarctation?

A

Infancy (severe) - heart failure, failure to thrive.

Later in life - hypertension.

41
Q

How might the coarctation show up on an Xray?

A

Rib notching.

42
Q

What does having Marfan’s syndrome put you at risk of?

A

Aneurysm and dissection. Aortic/mitral valve

43
Q

What does having Marfan’s syndrome put you at risk of (in terms of CV disease)?

A

Aneurysm and dissection. Aortic/mitral valve prolapse/regurgitation.

44
Q

How can Marfan’s impact on other systems in the body?

A

Impact on skeletal system, eyes (cataract, lens dislocation), lungs (pneumothorax).

45
Q

What mutation does Marfan’s stem from?

A

Fibrillin 1 gene - causes connective tissue weakness.