Brainscape's Knowledge GenomeTM

Browse over 1 million classes created by top students, professors, publishers, and experts.


See full index

Cardio Week 1 > Vascular Disease Basics > Flashcards

Vascular Disease Basics Flashcards

1
Q

What are advanced glycation end products (AGEs) ?

A

Process when glycated products are produced when an oxidative step is involved (ROS accelerates process) leading to glycated proteins, lipids, or nucleic acids (e.g. hemoglobin A1c)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What do AGEs do?

A
  • can induce cross linking of collagen which can cause vascular stiffening and entrapment of low-density lipoprotein particles (LDL) in artery walls
  • can glycate LDL which promotes its oxidation
  • can bind to RAGE and cause oxidative stress as well as activation of inflammatory pathways in vascular endothelial cells
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

How will someone with a ruptured Berry aneurysm present?

A

with pounding headache

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Where are Berry aneurysms common?

A

at branch points because there is more turbulence

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What layer of the vessel is thought to be the cause of a Berry aneurysm?

A

the media

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are the two forms of aneurysm?

A

Saccular and Fusiform

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are AV fistulas?

A

abnormal connections of artery and vein without capillary bed

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Fibromuscular dysplasia is common in what population?

A

younger women

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What vessel layer is thought to be the source of fibromuscular dysplasia?

A

media (75%)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What happens in fibromuscular dysplasia?

A

a ‘string of beads’ look caused by alternating thickening of the media affecting the distal 2/3 of the main renal artery

can lead to HTN (however, it is noninflammatory and nonathersclerotic)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are some cell wall markers?

A

CD31, CD34, D2-40

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is an ectasia?

A

a generic term for local dilatation of a structure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is a telangiectasia?

A

permanent dilatation of preexisting small vessels (usually in skin or mucous membranes)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are some types of vascular estasias?

A
  • nevus flammeus
  • spider telangectasias
  • Hereditary hemorrhagic telangectasia

can be congenital or acquired- not a true neoplasm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Describe nevus flammeus.

A

They are usually large flat patches of purple/red skin with well-defined borders. At birth the surface is flat but in time it becomes bumpy and often more unsightly

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

T or F. Nevus flammeus shrink by themselves and often disappear

A

F.

17
Q

Describe salmon patches.

A

common lesions that appear often at the nape of the neck (stork bite) or forehead between the eyebrows (aka angel’s kiss) that become more common when crying and often spontaneously disappear within the first year of life

18
Q

What is Sturge Weber syndrome?

A

port wine ectasia that distributes along the trigeminal nerve

19
Q

Why would imaging be appropriate with Sturge Weber syndrome?

A

because they often develop venous angiomas in the cortical leptomeninges

20
Q

What is Sturge Webber syndrome associated with physically?

A
  • mental retardation
  • seizures
  • hemiplegia
21
Q

What is the most common symptom of Hereditary hemorrhagic telangiectasia?

A

recurring nose bleeds

22
Q

Describe hemangiomas.

A
  • very common
  • composed of blood filled vessels
  • benign and malignant transformation is rare
23
Q

What are some types of hemangiomas (benign)?

A
  • Capillary hemangioma
  • Juvenile hemangioma
  • Pyogenic granulomas
  • Cavernous hemangioma
24
Q

Where are capillary hemangiomas common?

A
  • skin and subq
  • mucus membranes
  • liver, spleen and kidney
25
Q

What are juvenile hemangiomas?

A

a form of capillary hemangioma that usually presents in newborns and grow rapidly for a few months then fade by 1-3 yrs. Gone by 7 y/o completely

26
Q

Describe the histology of Juvenile hemangiomas.

A
  • mitotic figures may be present

- mast cells are present

27
Q

What are pyogenic granulomas?

A

capillary hemangiomas that grow rapidly in areas of trauma (often on skin, gingiva, oral mucosa) that typically bleed and ulcerate easily

28
Q

When are pyogenic granulomas particularly common?

A

pregnancy

29
Q

What hemangioma is associated with Von Hippel Lindau syndrome?

A

cavernous granulomas

30
Q

Cavernous lymphangiomas are associated with what?

A

Turner syndrome

31
Q

What are glomus tumors?

A

Benign, painful tumors commonly found under the nail bed that are proliferations of specialized smooth muscle cells of glomus body (thermoregulation)

32
Q

What does Kaposi sarcoma result in?

A

disruption of normal cell division (prevents apoptosis)

33
Q

What are the stages of Kaposi sarcoma?

A
  • patches- pink, red or purple typically on distal leg
  • plaque- larger, raised
  • nodular- more overtly neoplastic
34
Q

What things can cause angiosarcomas in the liver?

A
  • arsenical pesticides
  • Thorotrast (radioactive contrast agent)
  • Polyvinyl chloride

long latency period

35
Q

What things can cause angiosarcomas in lymphedema?

A

radiation- common in upper extremity after a radical mastectomy

Cardio Week 1 (22 decks)

Brainscape helps you reach your goals faster, through stronger study habits.
© 2024 Bold Learning Solutions. Terms and Conditions