Ch 7 Pathoma Vascular Path Flashcards

1
Q

____ is inflammation of the blood vessel wall. The etiology is usually ___. Most cases are/are not infectious. Divided into these three types, that comprise these 3 vessels

A

Vasculitis; unknown; are not; 1) large vessel = aorta and major branches; 2) medium vessel = muscular arteries that supply organs; 3) small = arterioles, capillaries, and venules

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2
Q

Arterial wall is comprised of these 3 layers

A

1) endothelial intimate
2) smooth muscle media
3) connective tissue adventitia

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3
Q

Name 2 clinical features of vasculitis

A

1) nonspecific symptoms of inflammation (fever, fatigue, weight loss, myalgias); 2) symptoms of organ ischemia (due to luminal narrowing or thrombosis of inflammed vessels)

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4
Q

In vasculitis, you can get symptoms of organ ischemia due to these 2 reasons

A

luminal narrowing or thrombosis of inflamed vessels (inflamed wall - healing - fibrosis - narrowing OR endothel damage - collagen exposed - clot formation - thrombus)

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5
Q

Name 2 types of large cell vasculitis and which vessels they classically involve

A

1) temporal (giant cell) arteritis (branches of carotid artery)
2) takayasu arteritis (aortic arch at branch points)

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6
Q

Temporal (___ cell) arteritis is a large vessel ___ vasculitis that classically involves branches of the ____. It is the most common form of vasculitis in ___ (age __), and usually affects females/males. Treatment is ___, and there is a high risk of __ w/o tx

A

giant; granulomatous; carotid; older adults; greater than 50; females; corticosteroids; blindness

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7
Q

Temporal (giant cell) arteritis presents with these 3 main symptoms (and why). This extra symptom is often present. And ___ is often elevated)

A

1) headache (temporal artery invlvmt); 2) visual disturbances (ophthalmic artery invlvmt); 3) jaw claudication (pain with chewing); 4) flu like symptoms with joint and muscle pain (polymalgia rheumatica); ESR

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8
Q

A biopsy of temporal giant cell arteritis reveals ___ vessel wall with __ and ___. Lesions are ___, so diagnosis requires bx of a long/short segment and a negative bx does/does not exclude disease.

A

inflamed; giant cells; intimal fibrosis; segmental; long; does not

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9
Q

Takayasu arteritis vs temporal giant cell arteritis: which one presents in adults over 50, which one presents in females, which one presents in asians, which one presents at the aortic arch branch points, which ones is granulomatous

A

giant cell; both; takayasu (young asian females); takayasu; both

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10
Q

Takayasu arteritis is large vessel ___ vasculitis that classically involves the ___ at branch points. Presents in ___ (age ___), and classically in ____. Treatment is ___.

A

granulomatous; aortic arch; adults less than 50; young asian females; corticosteroids

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11
Q

Takayasu arteritis presents with __ and ___ symptoms with a weak or absent __ in the upper extremity (‘____’ disease). ___ is elevated

A

visual; neurologic; pulse; pulseless; ESR

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12
Q

Name 3 types of medium vessel vasculitis

A

muscular arteries that supply organs - 1) polyarteritis nodosa; 2) kawasaki disease; 3) buerger disease

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13
Q

Polyarteritis nodosa is a medium vessel ___ vasculitis involving multiple ___, but sparing the ___. Classically presents in old/young adults with these 4 symptoms. It is associated with ___.

A

necrotizing; organs; lungs; young; 1) hypertension (renal artery invlvmt); 2) abdominal pain with melena (mesenteric artery invlvmt); 3) neurologic disturbances; 4) skin lesions; serum HBsAg

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14
Q

Polyarteritis nodosa involves lesions of varying stages. Early lesions consist of ___ inflammation with ___. It eventually heals with ___ producing a ‘____’ appearance on imaging. Tx is ___ and ___, and it is fatal if not treated

A

transmural; fibrinoid necrosis; fibrosis; string-of-pearls; corticosteroids; cyclophosphamide

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15
Q

Kawasaki disease is a medium cell vasculitis that classically affects ___ (___ age). Presents with ___ signs (including these 4). ___ artery involvement is common, which leads to risk for these two things. Tx is __ and __. Disease is self limited

A

Asian children; less than 4 years old; nonspecific; fever, conjunctivitis, erythematous rash of palms and soles, enlarged cervical lymph nodes; coronary; thrombosis with MI; aneurysm with rupture; aspirin and IVIG
(kawasaki motorcycle)

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16
Q

Fibrinoid necrosis can be seen in these two cases

A

vasculitis and malignant hypertension

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17
Q

Usually you don’t give aspirin to a child with a viral illness for risk of developing ___, but you do give aspirin to children with this disease.

A

Reye syndrome (rapidly progressive encephalopathy); kawasaki disease

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18
Q

Buerger’s disease is medium vessel ___ vasculitis involving the ___. It presents with ___, ___, and ___ of fingers and toes. ___ is often present. It is highly associated with ____, and tx is ____.

A

necrotizing; digits; ulceration, gangrene, autoamputation; Raynaud phenomenon; heavy smoking; smoking cessation

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19
Q

Name 4 types of small vessel vasculitis

A

arterioles, capillaries, venules - 1) Wegener granulomatosis; 2) Microscopic polyangiitis; 3) Churg-Strauss syndrome; 4) Henoch-Schonlein purpura

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20
Q

Wegener granulomatosis is a small vessel ___ ___ vasculitis involving these 3 locations. ____ levels correlate with disease activity. Bx reveals large ___ ____ with adjacent ___ ___. Treatment is ___ and ___. Relapses are common/rare.

A

necrotizing granulomatous; nasopharynx, lungs, kidneys; serum c-ANCA; necrotizing granulomas; necrotizing vasculitis; cyclophosphamide and steroids; common

“C” disease (wecener)

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21
Q

Wegener granulomatosis classically presents in a ___ female/male with these 3 symptoms.

A

middle-aged; male; 1) sinusitis or nasopharyngeal ulceration; 2) hemoptysis with bilateral nodular lung infiltrates; 3) hematuria due to rapidly progressive glomerulonephritis

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22
Q

Microscopic polyangiitis is a small vessel ___ vasculitis involving ____, especially __ and ___. Presentation is similar to Wegener granulomatosis except ___ and ___ are absent. ___ levels correlate with disease activity. Tx is ___ and ___. Relapses are common/rare.

A

vasculitis; multiple organs; lung and kidney; nasopharyngeal invlvmt; granulomas; p-ANCA; cyclophosphamide; corticosteroids; common

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23
Q

Churg-Strauss syndrome is a small vessel ___ ___ inflammation with ____ involving ____, especially ___ and ___. ___ and __ are often present. ___ levels correlate with disease activity

A

necrotizing granulomatous; eosinophils; multiple organs; lungs; heart; asthma; peripheral eosinophilia; serum p-ANCA

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24
Q

Of the small vessel vasculitis, which is/are granulomatous? p-ANCA? c-ANCA? involves lungs? eosinophils? IgA complex deposition

A

granulomatous: wegener and churg-strauss; p-anca: microscopic polyangiitis and churg-strauss; c-anca: wegeners; lungs: WG, MP, and CSS (these three are also all necrotizing); eosinophils: CSS; IgA: hence-shonelein purpura

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25
Q

What is the most common vasculitis in children?

A

Henoch-Schonlein purpura

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26
Q

Henoch-Schonlein Purpura is small vessel vasculitis due to ____. It presents with these 3 symptoms, and usually occurs following ____. Disease is self-limited, but may recur. Treated with ___ if severe.

A

IgA immune complex deposition; 1) palpable purpura on buttocks and legs; 2) GI pain and bleeding; 3) hematuria (IgA nephropathy); upper respiratory tract infection; steroids

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27
Q

____ is increased blood pressure. May involve __ or __ circulation. Systemic ___ is defined as pressure of greater than or equal to ___ mmHg (normal is less than ___mmHg). Can be divided into ___ or __ based on etiology.

A

Hypertension; systemic; pulmonary; HTN; 140/90; 120/80; primary; secondary

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28
Q

Primary HTN is due to ___ (95% of all HTN cases). Name 6 risk factors.

A

unknown etiology; age, race (african americans have increased risk, asians have decreased), obesity, stress, lack of physical activity, high salt diet

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29
Q

Secondary HTN (5%) is due to an identifiable etiology. ___ is a common cause.

A

renal artery stenosis (renovascular hypertension)

30
Q

Renal artery stenosis causes a increased/decreased blood flow to the glomerulus. The ___ responds by secreting ___, which converts ___ to ____. Angiotensin I is converted to ___, by ____, causing a rise/drop in blood pressure.

A

decreased; juxtaglomerular apparatus (JGA); renin; angiotensinogen; angiotensin I; angiotensin II; angiotensin converting enzyme (ACE); rise

31
Q

Angiotensin II raises blood pressure in these 2 ways.

A

1) contracting arteriolar smooth muscle, increasing total peripheral resistance
2) promoting adrenal release of aldosterone, which increases resorption of sodium in the distal convoluted table (expanding plasma volume)

32
Q

Aldosterone is released by the zone ___ of the adrenal ___, and increases/decreases resorption of sodium in the ___ of the kidney, resulting in expanding/contracting plasma volume.

A

glomerulosa; cortex; increases; distal convoluted tubule; expanding

33
Q

Secondary HTN due to renal artery stenosis causes HTN with increased plasma ___ and bilateral/unilateral atrophy of the kidney(s). Neither feature is seen in primary HTN

A

renin; unilateral atrophy of the affected kidney (due to low blood flow)

34
Q

Name 2 important causes of renal artery stenosis and who you see it in

A

1) atherosclerosis (elderly males)

2) fibromuscular dysplasia (young females)

35
Q

Fibromuscular dysplasia is a ___ defect of the ___, resulting in irregular thickening of __ and __ sized ___, especially the ___.

A

developmental; blood vessel wall; large; medium; arteries; renal artery

36
Q

Benign HTN is a ___ or ___ elevation in blood pressure. Most cases of HTN are benign/malignant. Benign HTN is ___, and it causes ___ and ___ damage quickly/slowly.

A

mild; moderate; benign; clinically silent; vessel; organ; slowly (over time)

37
Q

Malignant HTN is ___ elevation in blood pressure (greater than ____), comprises __% of HTN cases. May arise from ___ or ___. Presents with ___ (name 3) and is a medical emergency

A

severe; 180/120; 5; preexisting benign HTN; de novo; acute end-organ damage (e.g. acute renal failure, headache and papilledema)

38
Q

Arteriosclerosis is literally ___ due to ___ of the blood vessel wall. Name the 3 pathologic patterns

A

hard arteries; thickening; 1) atheroscerosis (intima of L/M bv’s); 2) arteriolosclerosis (small bv’s hyaline or hyper plastic); 3) Monckeberg medial calcific sclerosis (media) of medium arteries)

39
Q

Atherosclerosis is a ___ that obstructs blood flow. It consists of a ___ core (mostly ___) with a ___ cap. It often undergoes ___.

A

intimal plaque; necrotic lipid; cholesterol; fibromuscular; dystrophic calcification

40
Q

Atherosclerosis involved __ and __ sized arteries. Name the 4 most commonly affected.

A

large; medium; abdominal aorta; coronary artery; popliteal artery; internal carotid artery

41
Q

Name 4 modifiable risk factors for atherosclerosis

A

1) hypertension; 2) hypercholesterolemia (LDL increases risk, HDL decreases); 3) smoking; 4) diabetes

42
Q

Name 3 non-modifiable risk factors for atherosclerosis

A

1) age (number and severity of lesions increase with age); 2) gender (increased risk in males and postmenopausal women - estrogen is protective); 3) genetics (multi-factorial but family hx is highly predictive of risk)

43
Q

How does gender affect your risk for atherosclerosis?

A

increased risk in males and postmenopausal females (since estrogen is protective)

44
Q

In atherosclerosis formation, damage to ___ allows __ to leak into the ___. Lipids are ___, and then consumed by ___ via ___ receptors, resulting in ___ cells. Inflammation and healing leads to deposition of ___ and proliferation of ___.

A

endothelium; lipids; intima; oxidized; macrophages; scavenger; foam; extracellular matrix; smooth muscle

45
Q

Morphologically, early atherosclerosis begins as ___ (flat yellow lesions of the ___ consisting of ___). This begins early/late in life (present in most ___). Then it progresses to ____.

A

fatty streaks; intima; lipid-laden macrophages; early; teenagers; atherosclerotic plaque

46
Q

Name 4 complications of atherosclerotic plaques

A

1) stenosis of medium-sized vessels results in impaired blood flow and ischemia (PVD, angina, ischemic bowel disease); 2) plaque rupture w/thrombosis (MI, stroke); 3) plaque rupture w/embolization; 4) weakening of vessel wall (aneurysm)

47
Q

Atherosclerosis can cause stenosis of medium sized vessels resulting in impaired blood flow and ischemia leading to these 3 symptoms. When do you start to see symptoms?

A

1) peripheral vascular disease (lower extremity arteries like popliteal); 2) angina (coronary arteries); 3) ischemic bowel disease (mesenteric arteries); when artery is stenosed more than 70%

48
Q

A major complication of atherosclerosis occurs when plaque ruptures leading to ___, which can result in ___ (coronary artery) and ____ (middle cerebral artery)

A

thrombosis; MI; stroke

49
Q

Plaque rupture with embolization results in ___, characterized by ___ within the embolus

A

atherosclerotic embolus; cholesterol crystals (looks like cholesterol clefts)

50
Q

Arteriolosclerosis is narrowing of ___. It is divided in to these 2 types.

A

small arterioles; hyaline and hyperplastic types

51
Q

Hyaline arteriolosclerosis is caused by ___ into the vessel wall, producing vascular thickening/thinning. ____ are seen as pink hyaline on microscopy. It is a consequence of these 2 things.

A

proteins leaking; thickening; proteins; long-standing benign hypertension or diabetes

52
Q

Hyaline arteriolosclerosis results in reduced ___ with end-organ ___. Classically it produces ___ that slowly progresses to ____.

A

vessel caliber; ischemia; glomerular scarring (arteriolonephrosclerosis); chronic renal failure

53
Q

Hyperplastic arteriolosclerosis involves thickening/thinning of the vessel wall by hyperplasia of ____ (with a ‘____’ appearance). It is a consequence of ____, and results in reduced ___ with end-organ ___.

A

thickening; smooth muscle; onion-skin; malignant hypertension; vessel caliber; ischemia

54
Q

Hyperplastic arteriolosclerosis may lead to ___ necrosis of the vessel wall with ___. Classically causes ___ with a characteristic ‘____’ appearance

A

fibrinoid; hemorrhage; acute renal failure; flea-bitten (pinpoint hemorrhages due to blood vessels being blown out)

55
Q

Which arteriolosclerosis type is a consequence of benign HTN? malignant HTN? causes reduced vessel caliber with end organ ischemia? causes acute renal failure? chronic renal failure? caused by diabetes?

A

hyaline; hyperplastic; both; hyperplastic; hyaline; hyaline

56
Q

____ is calcification of the media of muscular (medium-sized) arteries. It is non-obstructive and is not clinically significant. Seen as incidental finding on x-ray or mammography

A

Mönckeberg Medial Calcific Sclerosis

57
Q

Aortic dissection is a __ tear with dissection of blood through the __ of the aortic wall. It occurs in the proximal/distal __cm of the aorta (high stress region) with ___ weakness of the media.

A

intimal; media; proximal; 10; pre-existing

58
Q

What is the most common cause of aortic dissection? What else is it associated with? What group presents with each?

A

hypertension: older adults

inherited defects of connective: tissue younger individuals

59
Q

Hypertension results in ____ of the vasa vasorum. Decreased flow causes ___ of the media, and can ultimately cause an aortic dissection.

A

hyaline arteriolosclerosis; atrophy

60
Q

These 2 inherited connective tissue defects classically lead to weakness of the connective tissue in the ___ (cystic medial necrosis). What do the defects affect?

A

media;
Marfan syndrome: defect of fibrillin (what elastic fibers are laid down on)
Ehlers-Danlos syndrome: defective formation of collagen

61
Q

How does aortic dissection present?

A

Sharp, tearing chest pain that radiates to the back

62
Q

Name the 3 complications of aortic dissection and the one that is the most common cause of death

A

1) pericardial tamponade (most common cause of death); 2) rupture with fatal hemorrhage; 3) obstruction of branching arteries with resultant end-organ ischemia (renal or coronary)

63
Q

Thoracic aneurysm is a ___-like ___ of the thoracic aorta. It is due to ___ in the aortic wall. Classically seen in this disease, which causes ___ of the ___ resulting in ___ narrowing, decreased __, and ___ of the vessel wall. Results in a “___” appearance of the aorta.

A

balloon; dilation; weakness; tertiary syphilis; endarteritis (inflammation of small vessels); vaso vasorum; luminal; flow; atrophy; tree-bark

64
Q

What is the major complication of thoracic aneurysm? Name 3 others.

A

dilation of the aortic valve root resulting in aortic valve insufficiency; 1) compression of mediastinal structures (airway or esophagus); 2) thrombosis; 3) aneurysm

65
Q

Abdominal aortic aneurysm is a __-like __ of the abdominal aorta. Usually arises below ___ but above __. It is primarily due to ___, and is classically seen in male/female ___ (greater than __ years old) with ___.

A

balloon; dilation; renal arteries; aortic bifurcation; atherosclerosis; male; smokers; 60; hypertension

66
Q

Atherosclerosis can lead to abdominal aneurysm by increasing the ___ to the media, resulting in __ and __ of the vessel wall. Abdominal aneurysm present as a ___ that grows with time

A

diffusion barrier; weakness; atrophy; pulsatile abdominal mass

67
Q

What is the major complication of abdominal aneurysm? And what is the triad presentation? Name 3 other complications

A

rupture (especially when >5 cm in diameter); hypotension (since bleeding), pulsatile abdominal mass, flank pain; 1) compression of local structures (ureter); 2) thrombosis; 3) embolism

68
Q

Hemangioma is a benign/malignant tumor comprised of ___. Commonly present at ___. Often regresses/grows during childhood. Most often involves ___ and ___.

A

benign; blood vessels; birth; regresses; skin; liver

69
Q

Angiosarcoma is a benign/malignant proliferation of ___. It is highly aggressive. Common sites include these 3.

A

malignant; endothelial cells; skin, breast, liver

70
Q

Name 3 exposures associated with liver angiosarcoma

A

1) polyvinyl chloride (PVC); 2) arsenic; 3) Thorotrast

71
Q

Kaposi sarcoma is a high/low grade benign/malignant proliferation of ___. It is associated with ___. Presents as ___, ___, and __ on the skin. May also involve __ organs.

A

low; malignant; endothelial cells; HHV-8; purple patches, plaques, nodules; visceral

72
Q

Name the 3 groups Kaposi sarcoma is classically seen in and the treatment for each

A

1) older eastern european males (tumor remains localiized to skin - tx surgical removal)
2) AIDS (tumor spreads early - tx anti-retroviral agents to boost immune system)
3) transplant recipients (tumor spreads early - tx involves decreasing immunosuppression)