Vasculitis Flashcards

1
Q

what is temporal arteritis?

A

a granulomatous vaculitis of large and medium sized vessels that predominantly affects the branches of the external carotid. Symptoms of PMR also commonly seen alongside

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2
Q

what are the S&S of GCA?

A

headache - typically over temporal or occipital areas

temporal artery and scalp tenderness (e.g pain when combing hair)

jaw claudication (pain on chewing)

thickening and nodularity of temporal artery and its branches

PMR symptoms

absent temporal artery pulse

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3
Q

what InV are done in temporal arteritis?

A

FBC

  • normocytic normochromic anaemia
  • mildly elevated WBC
  • increased platelets

Increased ESR and CRP

LFTs midly elevated

Temporal artery US
- wall thickening (halo sign), stenosis or occlusion

Temporal artery biopsy

  • gold standard for Dx
  • granulomatous inflammation with multinucleated gaint cells
  • skip lesions so can be missed
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4
Q

what is the treatment for GCA?

A

Prednisolone
Aspirin
Tocilizumab or MTX for relapsing disease

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5
Q

what are the complications of CGA?

A

vision loss
Glucorticoid side effects
aortic aneurysms
large vessel stenosis

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6
Q

what is polyarteritis nodosa?

A

a necrotising vasculitis that causes aneurysms and thrombosis in medium sized arteries leading to infarction in affected organs with severe systemic symptoms

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7
Q

what are the S&S of polyarteritis nodosa?

A
fever, weight loss and myalgia 
mononeuritis multiplex 
parasthesiae 
abdo pain (ischaemia of abdo organs) 
skin manifestations (ulcers, purpura, eruption) 
high diastolic BP
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8
Q

what InV are done in polyarteritis nodosa?

A

FBC

  • increased WCC
  • mild eosinophilia
  • Anaemia

Increased ESR and CRP

ANCA -ve

renal or mesenteric angiography

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9
Q

how is polyarteritis nodosa treated?

A

BP control

Corticosteriods or cyclophosphamide

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10
Q

what is Henoch-Schonlein purpura ?

A

the most common vasculitis of childhood which affects the small vessels. It is characterised by a tetrad of

  • rash
  • abdo pain
  • arthritis/arthralgia
  • glomerulonephritis
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11
Q

what can trigger HSP?

A

URTI or streptococcal infections

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12
Q

what are the S&S of HSP?

A

arthralgia
- knees and ankles commonly

Abdo pain
- often associated with N&V

Skin rash

  • palpable non-blanching purpura
  • extravasation of blood into skin
  • usually on lower extremities

nephritic signs
- haematuria, proteinuria, high BP

scrotal pain/swelling, headaches and seizures may manifest

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13
Q

what InV are done in HSP?

A

urinalysis
- RBCs, proteinuria or casts

24hr urinary protein
- may be elevated due to renal involvement

Serum IgA
- raised

renal biopsy
- IgA in mesangium

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14
Q

what is the treatment of HSP?

A

analgesia
corticosteroids
plasmapharesis

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15
Q

what is granlumomatosis with polyangiitis? (Wegener’s)

A

a systemic vasculitis that typically involves small and medium sized vessels. Although any organ can be affected, the classical triad consists of;

  • upper respiratory tract involvement
  • lower respiratory tract involvement
  • pauci-immune glomerulonephritis
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16
Q

what autonantibody is associated with Granulomatosis with polyangiitis?

A

ANCA

17
Q

what are the S&S of GWP?

A

upper airway

  • rhinitis
  • chronic sinusitis
  • saddle nose deformity

lower airway

  • parenchymal nodules
  • haemoptysis
  • SOB
  • chest pain
  • crackles and reduced A/E

renal
- nephritic symptoms

constitutional symptoms

  • fatigue
  • weight loss
  • fever and night sweats
18
Q

what InV are done in GWP?

A

urinalysis and microscopy
- haematuria, proteinuria and RBCs

CT chest
- lung nodules and infiltrates

ANCA

FBC
- anaemia

ESR elevated

creatinine elevated

19
Q

what is the treatment of GWP?

A

corticosteroids and cyclophosphamide
plasmapharesis
pneumocystitis jirovecii prophylaxis