Blood Vessels Pathology Flashcards

1
Q

[syndrome]

gain of function of ENaC channel resulting to increased Na reabsorption and then hypertension

A

Liddle Syndrome

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2
Q

Associated condition

eosinophilic hyaline material with associated luminal narrowing

A

essential hpn

DM

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3
Q

[associated condition]

concentric, laminated thickening, onion skin lesion, note of fibrinoid deposition and vessel wall necrosis

A

malignant hypertension

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4
Q

location of neovascularization in an atheromatous plaque

A

periphery

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5
Q

[clinical phase of atherosclerosis]

mural thrombosis, embolization, and wall thickening can lead to

A

aneurysm and rupture

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6
Q

[clinical phase of atherosclerosis]

plaque rupture, plaque erosion, plaque hemorrhage, mural thrombosis, embolization can lead to

A

occlusion by thrombus

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7
Q

[clinical phase of atherosclerosis]

progressive plaque growth can lead to

A

critical stenosis

usually 70%

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8
Q

the larger the lipid core, the ____stability of the plaque

A

greater the stability of the plaque

Remember, size of lipid core is inversely proportional to stability

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9
Q

the lesser the degree of inflammation, the ____ stability of the plaque

A

greater stability

remember, degree of inflammation is inversely proportional to stability

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10
Q

the thicker the fibrous cap, the ___ stable the plaque

A

more stable the plaque

fibrous cap is directly proportional to stability

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11
Q

[dissection]

intima tear involvinf the descending aorta only.

What is the standford classification?

A

Stanford B

DeBakey III = Standford B

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12
Q

[aortic dissection]

Both ascending and descending aorta are involved.

What is it s debakey classification?

A

DeBakey I

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13
Q

[diagnosis?]

45/M, hypertensive with marfan syndrome.

Noted sudden, excruciating anterior chest pain, radiating to the back and downward

A

aortic dissection

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14
Q

[syndrome]

Non-infectious small artery vasculitides, p-anca positive

A

churg-strauss syndrome

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15
Q

[syndrome]

non-infectious small artery vasculitides, c-anca positive

A

Wegener granulomatosis/ granulomatosis with polyangitis

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16
Q

[diagnosis]

headache among elderly individual, along course of superficial temporal artery, associated with multiple joint pains

A

giant cell arteritis

17
Q

[diagnosis]

affects large vessels of the aortic arch, notable ocular disturbances and weakened UE pulses

18
Q

[diagnosis]

associated with hepatitis B, renal and visceral vessels (NEVER PULMONARY)

clinically, HPN and visceral ischemia

prominent fibrinoid necrosis, segmental, transmural, necrotizing

A

polyarteritis nodosa

19
Q

[diagnosis]

fever >5 days, conjunctival injection, mucosal erythema, cervical lymphadenopathy, polyamorphous exanthem

A

kawasaki disease

20
Q

important cause of MI in children; can cause coronary artery aneurysm

less prominent fibrinoid necrosis, segmental, transmural, necrotizing

A

kawasaki disease

21
Q

[diagnosis]

associated with connective tissue disorders

common in kidney and LUNG; hemoptysis, hematuria

A

microscopic polyangitis

PAN = no lung involvement

22
Q

[diagnosis]

associated with asthma, allergic rhinitis, eosinophilia

noted involvement of cutaneous, GIT, renal and cardiac vessel

Clinically, palpable purpura, GI bleed and FSGS

A

churg-strauss syndrome

23
Q

[diagnosis]

PAN + extravascular necrotizing granulomas and hypereosinophilia

A

Churg-strauss syndrome

Remember, atopy/eosinophilia = sneeze = aaachooo = aaaachurg

24
Q

[diagnosis]

fragmented PMNs in post capillary venule (leukocytolasia)

A

Microscopic polyangitis

25
[diagnosis] prominent pulmonary involvement, may also involve renal vessels necrotizing granulomas of respiratory tract, necrotizing or granulomatous vasculitis, focal segmental necrotizing GN c-ANCA positive
Wegener granulomatosis
26
[diagnosis] recurrent oral aphthous ulcers, genital ulcers, uveitis, neutrophilic infiltration of vessels small to medium sized vessels are affected
Behcet syndrome
27
[diagnosis] strongly associated with cigarette smoking, small to medium vessel involvement, reynaud phenomenon, intermittent claudication, thrombosis with microabcesses
buerger disease Thromboangitis obliterans
28
most important risk factor for lower extremity DVT
prolonged immobilization
29
[diagnosis] migratory superficial vein thrombophlebitis in cancer patient
trosseau syndrome
30
[diagnosis] lower extremity edema, superficial abdominal vein distention, massive proteinuria (if renal vein is involved)
IVC syndrome
31
most common cause of lymphangitis and lymphedema
GABHS
32
[diagnosis] facial port wine nevi, ipsilateral leptomeningeal cortical venous angiomas, mental retardation, seizures, hemiplegia, skull radioopacities
Struge-Weber syndrome
33
[diagnosis] AD defect in TGF beta telangectasia on skin, oral mucosa, respiratory, GIT, urinary tract
Osler-weber-rendu disease
34
[diagnosis] rapidly growing, red, pedunculated lesion on the skin, gingival or oral mucosa
pyogenic granuloma
35
cavernous lymphangiomas of the neck is more common in ___ syndrome
Turner
36
[diagnosis] african, <40 years old, HIV negative, HHV 8
Endemic Kaposi Sarcoma
37
[diagnosis] | HHV 8 in HIV positive patients
epidemic kaposi sarcoma
38
Thorotrast exposure is associated with this malignant tumor
hepatic angiosarcoma
39
Stains used in angiosarcomas
CD31, CD34, vWF