Unit 3 - CVD Pt 2 Flashcards

1
Q

lupus ratio/incidence

A

female:male 8:1

peak incidence in 40s

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2
Q

lupus etiology

A

Autoimmune etiology
Antigen-antibody Immune complexes formed
Antibodies formed to DNA

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3
Q

types of lupus

A

Discoid (skin)
Systemic (SLE-skin & Internal organs)
- 30% have Rheumatoid factor

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4
Q

skin

A

if on scalp - alopecia
- scarring, esp with sunlight
butterfly rash - 80%
- capillary dilations on skin: telangiectasis

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5
Q

joints

A
Polyarthritis, asymmetrical
Inflammatory joint disease
Pannus
Cartilage Destruction
Osteophytes
Narrow joint space
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6
Q

kidneys

A

Nephrovasculitis
Nephritis
Renal Vessels are Partially Occluded

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7
Q

Renal induced hypertension

A

Decreased blood flow through the kidney causes the kidney to release renin

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8
Q

hypertensive crisis

A
Systolic BP >180 mmHg
Diastolic BP >110 mmHg)
Increased Intracranial pressure
Seizures
Intracranial hemorrhage
Ventricular dysfunction
Dysrhythmias
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9
Q

mucous membranes

A

autoantibodies have affected collagen, causing nodule and ulcer formation in mouth

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10
Q

CNS/PNS

A

localized nodules that result in memory loss, dementia, and seizures
involvement in PNS can cause both sensory and motor loss

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11
Q

liver

A

hepatic nodules with scarring can decrease liver function

can lead to liver failure

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12
Q

lungs/pleura

A

Pleural Fibrosis
Pleural inflammatory nodule formation
Interstitial Lung Disease

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13
Q

cardiovascular system

A

Valvulitis
Mitral Valve Nodule formation on the suggests a stenotic valve
Myocarditis-note the inflammatory lesions/nodules
Generalized Vasculitis
Vessel Occlusion

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14
Q

vascular system

A

Aneurysm: Abnormal blood flow, Thrombus (clot), Vessels may leak or Rupture
Abdominal Aortic Aneurysm (Triple A)
Most common site of Aneurysm Formation

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15
Q

Raynaud’s

A

40%

fingers become white from lack of blood flow, then blue as vessels dilate and red when blood returns

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16
Q

SLE evaluation criteria (3)

A
Most will have a blood dyscrasia
Counts will be reduced < Normal
1. Anemia (hypochromic, microcytic) 
2. Thrombocytopenia (low platelet count)
3. Leukocytopenia (low WBCs)

Skin lesions/rash
Butterfly rash
Arthralgia (due to arthritis)

17
Q

Serological Findings

A

Rheumatoid factor (30%)
Antinuclear Antibody or ANA (95%)
Antibodies against proteins in cell nuclei
+LE cells (1948)
+ Anti-Smith (anti-Sm) antibodies: Bind to RNP in the cell nucleus
+ Anti-ribonuclear protein (anti-RNP) antibodies: Bind to RNP in the cell nucleus

18
Q

LE cell

A

An LE cell is a neutrophil or macrophage that has phagocytized (engulfed) the nuclear material of another cell.

nucleus is pushed to one side and flattened against the cell membrane of the PMN

19
Q

scleroderma

A

CVD that causes the skin to become dense, fibrous, thickened, and tight

F:M 3:1

20
Q

types of scleroderma

A
Skin (Morphea) type
Systemic Type (Systemic Sclerosis)
Skin plus internal organs
drawn pursed
lips, shiny skin over the
cheeks and forehead, and
atrophy of muscles of the
temple, face, and neck.
21
Q

appearance of scleroderma

A

Skin tightness
Mauskopf (Mouse head) face
Telangiectasias
Raynaud’s

22
Q

Scleroderma variants:

Diffuse Systemic Sclerosis

A

Seen in some people with systemic sclerosis

Can be aggressive with poor prognosis

23
Q

Scleroderma Variants:

C R E S T Variant

A

Variant-seen in most people with systemic sclerosis

CREST is an acronym for:
Calcinosis   
Raynaud’s      
Esophageal dysfunction    		
Sclerodactyly (sausage fingers/toes)
Telangioectasias (dilation of small vessels causes flat red marks on skin)
24
Q

Serological markers of scleroderma

A
\+Rheumatoid factor (<10%)
\+ ANA (60-80%)
Anti-topo-isomerase I antibody
Anti-centromere  antibody (CREST)
Anti-Th/To antibody 
Anti-U3 small nuclear ribonucleoprotein (snRNP) antibody