Rheumatological and Autoimmune Flashcards

1
Q

What are the most common autoimmune antibodies seen in vasculitis and how are they screened for, and what following procedure should be done if one is discovered?

A

Anti- Neutrophil Cytoplasmic Antibodies/ ANCAs
- indirect immunofluorescence

ELSIA testing to establish:

  • Proteinase - 3
  • Myeloperoxidase
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2
Q

What is the common vasculitis that affects the large vessels, and who is affected? and what are the symptoms

what are some complications?

A

Giant cell vasculitis:

Females, >50, white

Headache

Jaw pain

Visual disturbance

polymyalgia

complications:
blindness
- amaurosis tagux pattern

Stroke

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3
Q

Out line pathophysiology of giant cell vasculitis:

A

T cell mediated immune response.
granulomatous inflammation - with giant cell and lymphocyte infiltration.

fibrosis occurs, endothelial damage. thrombogenic.

disease is segmental across the vessel.

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4
Q

What are some diagnostic findings of giant cell?

A

Increased ESR > CRP

Temporal pain

Pulseless temporal vessels

  • *biopsy of temporal artery
  • mononuclear infiltration
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5
Q

What is the treatment of giant cell vasculitis?

A

Prednisolone
- even before confirmation of biopsy

or

IV methylprednisolone if eye problems.

+

Aspirin 75mg for clots

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6
Q

Name the common, ANCA negative small vessel vasculitis, and what are the areas it predominantly affects?

A

Henock Schonlein disease

skin, GI, kidneys and joints

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7
Q

Who gets Henock Schonlein disease, and what are the typical symptoms:

A

Children
Males

  • palpable purpura rash
  • mainly on buttocks
  • ecchymosis
  • Urticaria rash
  • G.I pain

complications:

  • polyarthritis
  • glomerulonephritis
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8
Q

What is the pathological process behind Henock Schonlein disease?

A

Previous group A Strep infection.

cross reacts causing type III hypersensitivity reaction with IgG forming against the IgA

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9
Q

Name a ANCA positive vasculitis, and list who gets it and common symptoms:

A

Granulomatous Angiitis

middle ages men

  • sinusitis
  • nasopharyngeal ulceration
  • haemoptysis
  • bilateral lung nodules
  • haematuria

**nasopharynx
lungs
kidneys `

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10
Q

What investigations should be done for granulomatous angiitis vasculitis?

A

Serum c- ANCA levels

biopsy
- necrotic granulomas

high protein to serum creatinine level

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11
Q

What’s the treatment for granulomatous angiitis?

A

Cyclophosphamide

Steroids

Rituximab

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12
Q

What vasculitis is biggest cause of an MI in children?

A

Kawasaki Vasculitis

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13
Q

What are the symptoms of Kawasaki vasculitis and how is it treated?

A
  • fever
  • conjunctivitis
  • strawberry tongue
  • erythematous rash on palsm and soles

Treated with:

  • aspirin
  • IgG immunoglobulins
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14
Q

list the common types of seronegative arthritis:

A

Ankylosing spondylitis

Reactive arthritis

Psoriatic arthritis

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15
Q

What is associated with HLA DR3?

A

Systemic Lupus, Grave’s disease, Diabetes Melitus

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16
Q

What is associated with HLA DR4?

A

RA

17
Q

What is associated with HLA DR2?

A

MS

18
Q

When measuring the intra-compartment pressure of a suspected compartment syndrome, how close should the area be measured to the suspected source? and what pressure is a strong indicator of a fasciectomy?

A

within 5cm

20-30 mmHg above diastolic pressure

19
Q

What is the treatment of compartment syndrome?

A

Remove cast

Open fasciaectomy
- do not stiture back until has completely healed over

20
Q

How are Rheumatoid and SLE different in terms of their joint involvement?

A

Rh causes joint destruction, whereas SLE does not cause joint destruction, only deformity which when moved goes back into place

21
Q

Whats a common symptoms seen in both systemic sclerosis and SLE?

A

Raynaud’s

22
Q

What drug do you give for Psoriatic arthritis and Psoraisis?

A

Apremilast

23
Q

Name some differentials for rheumatoid disease:

A

Psoriatic arthritis

Lupus

Osteoarthritis

Infective O/A