Vascular Path Robbins Part 2 Flashcards

1
Q

aneurysm

A

localized abnormal dilation of a BV

-may be congenital or acquired

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2
Q

true aneurysm vs false aneurysm

A
  • true- intact (but thinned) muscular wall

- false- defect thru the vessel wall or heart, communicating with an extravascular hematoma (“pulsating hematoma”)

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3
Q

saccular vs fusiform aneurysms

A
  • saccular- spherical

- fusiform- diffuse, circumferential dilations of a long vascular segment

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4
Q

aneurysm- caused by?

A
  • defective vascular wall CT
  • net degradation of vascular wall CT
  • weakening of vascular wall by ischemia (atherosclerosis, HTN, tertiary syphilis)
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5
Q

defective vascular wall CT- causes

A
  • Marfan syndrome (fibrill def)
  • Loeys-Dietz syndrome- mutations in TGF-B R’s- def syn of elastin and collagens I, III
  • Ehlers-Danlos syndrome- def type III collagen syn
  • vit C def- altered collagen cross-linking
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6
Q

net degradation of vascular wall CT- causes

A
  • inflammation and assoc proteases
  • matrix metalloprotease (MMP)- degrade extracellular matrix in aretrial wall
  • dec expression of TIMPs (tissue inhibitors of MMP)
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7
Q

weakening of vascular wall by ischemia- causes

A
  • loss of smooth m or syn of noncollagenous or nonelastic ECM
  • inner media ischemia- atherosclerosis
  • outer media ischemia- HTN (vaso vasorum narrowed)
  • tertiary syphilis- obliterative endarteritis of vaso vasorum of thoracic aorta
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8
Q

aneurysm - loss of vascular wall elastic tissue or ineffective elastin syn- leads to final common result of diff conditions??

A

-cystic medial degeneration- with disorganized elastin filaments and increased ground substance (proteoglycans)

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9
Q

2 most important causes of aortic aneurysms

A
  • atherosclerosis (abdominal aorta)

- HTN (thoracic aorta)

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10
Q

abdominal aortic aneurysm- due to? occurs where? more frequent in?

A
  • atherosclerosis!
  • usually below renal a’s; often involve common iliac a’s
  • men, smokers, 6th decade of life
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11
Q

abdominal aortic aneurysm- characterized by? complications?

A

severe atherosclerosis of aorta, covered with mural thrombus

  • pulsating mass in abdomen!
  • rupture, hemorrhage
  • occlusion of branching a’s, downstream ischemia
  • embolism
  • impingement on another structure
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12
Q

abdominal aortic aneurysm- rupture risk related to?

A

aneurysm size!

->5 cm- managed surgically! (11% risk)

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13
Q

3 AAA variants

A
  • infl AAA (5-10%)- younger pts, back pain, elevated infl markers- localized immune response to aortic wall
  • IgG4-related disease- high plasma levels of IgG4 and tissue fibrosis
  • mycotic AAA- lesions infected by the lodging of circulating microorganisms in the wall
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14
Q

thoracic aortic aneurysm- caused by? clinical presentation?

A
  • HTN or less commonly Marfan syndrome!
  • impingement- lower resp tree, esophagus, recurrent laryngeal n’s (cough)
  • aortic valvular insuff
  • pain- erosion of bone
  • rupture
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15
Q

aortic dissection- occurs when? occurs in who? primary risk factor? classic presentation?

A

blood enters a defect in the intima- travels within layers of aortic media

  • HTN males (40-60); Marfan’s syndrome, rarely in pregnancy
  • HTN!!
  • severe chest pain, radiating to back b/w scapulae
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16
Q

major risk factor for aortic dissection

A

HTN

-medial hypertrophy of vasa vasorum with degenerative changes

17
Q

aortic dissection pathogenesis, most occur where?

A
  • blood enters aortic wall via an intimal tear- forms an intramural hematoma
  • in HTN pts- have some degree of cystic medial degeneration
  • most in ascending aorta
18
Q

aortic dissection- type A and B

A
  • A- more common, higher morbidity and mortality- adj to aortic root!- treat with antiHTN therapy, surgical repair (deBakey types 1 and II)
  • B- distal not involving the ascending part (deBakey type III