Autoimmune Diseases Flashcards

1
Q

In most cases of autoimmunity there is thought to be a_____ factor that acts on a _____ susceptible individual

A

environmental, genetically

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2
Q

Name all the symptoms of lupus and how many of them are needed to make a diagnosis

A

Malar rash, discoid rash, photosensitivity, oral ulcers, arthritis, renal disorder, hematological disorder, immunological disorder (anti ds DNA, anti Smith , Antiphospholipid antibody), neurological disorder, antinuclear antibody/ 4 out of 11 needed

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3
Q

systemic lupus erythematosus has what two unique antibody systems in abundance

A

anti ds DNA, anti Smith

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4
Q

drug induced lupus erythematosus has what unique antibody system in abundance

A

anti histone

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5
Q

Describe the pathogenesis of lupus

A

genes involved include MHC II and complement–> apoptotic bodies fail to clear out–> nucleosmal proteins and self antigens present–> T-cells and B-cells specific for the self antigens activate–> IgG autoantibody production–> immune complexes (Type III) or autoantibody (Type II) mediated tissue injury

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6
Q

What is included in a full house granular deposition?

A

IgA, IgG, IgM, C3, C1q (C4)

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7
Q

What kind of effect does lupus have on the heart?

A

Can lead to fibrinous pericarditis/cardiac rub, can also leave libman-sacks deposits on mitral valve and cardiac wall

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8
Q

What are the class of lupus glomerulonephritis and which ones are dangerous?

A

Class I: Normal (not dangerous)
Class II: Mesangial (not dangerous)
Class III: Focal proliferative (dangerous)
Class IV: Diffuse proliferative (dangerous)
Class V: Membranous (protein in urine but not destruction)
Class VI: Diffuse sclerosing (RIP)

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9
Q

What is the difference between Class III and Class IV lupus glomerulnephritis

A

Class III is 50% glomeruli affected

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10
Q

For Class III and Class IV lupus glomerulnephritis, describe the location and process of degradation

A

The immune complexes are next to the endothelium lining–> fenestrae between the endothelial allow complement to enter–> immune complexes convert complement to C5a which recruits neutrophils–> decreased levels of complement in the serum due to this happening in the kidney

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11
Q

Where is membranous lupus located in kidney cells?

A

Subepithelium–> effect podocytes thus letting proteins enter urine

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12
Q

Whats the difference between lupus arthritis and rheumatoid arthritis?

A

Lupus arthritis does not have joint deformity

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13
Q

CNS lupus is usually caused by what?

A

Angioplsty associated with antiphospholipid antibodies

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14
Q

What time of day does Rheumatoid arthritis joint pain usually feel worse?

A

Morning

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15
Q

What two test are used to confrim Rheumatoid arthritis?

A

Rheumatoid factor, anti CCP

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16
Q

This disease usually involves the HLA-B27 genes, involves ligament attaching to bone, the sacroilliac joint, and is absent in RF and anti-CCP

A

Seronegative Spondyloarthropathies

17
Q

What disease specifically leads to the loss of lumbar lordosis?

A

Ankylosing spondylitis

18
Q

This autoimmune disease involves xerostomia and keritanoconjunctivitis sicca because it is thought that T-cells destroy salivary and lacrimal glands, has SS-A and SS-B antibodies, is associated with RA and RF, and increases the incidence of B-cell lymphoma by 40x

A

Sjogren Syndrome

19
Q

This disease involves the Scl-70 antibody and has a nucleolar ANA

A

Diffuse scleroderma

20
Q

This disease involvs the CREST symptoms and has anticentromere antibodies

A

Limited scleroderma

21
Q

A marked sign of sceleroderma is diffuse____ in the tissue

A

fibrosis and intimal thickening (no immune deposits)

22
Q

When the skin turns from white to blue to red after being exposed to cold

A

raynuad’s phenomenon

23
Q

This autoimmune disease leads to difficulty in rising from a chair or climbing stairs, and involves the infiltration of lymphocytes into muscle, heliotrope eyes

A

Inflammatory myopathy

24
Q

This disease is a combination of SLE, scleroderma, and inflammatory myopathy, involves antibodies to RNP, and causes little renal disease and responds well to steroids

A

Mixed connective tissue disease