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Pathology

Inflammatory vasculitis in small and medium-sized arteries occur mainly at bifurcations and branch points. Aneurysms develop in the weakened vessel, carrying a subsequent risk for rupture and hemorrhage
Nodosa’ are small aneurysms produced by fibrotic healing.

Aetiology

The cause is unknown, but viral infections such as HIV, CMV, HBV are associated with Polyarteritis Nodosa.

Signs

Raised BP, fever, livedo reticularis, mononeuritis multiplex 

Symptoms

Fever, malaise, anorexia and weight loss, myalgia and arthralgia. 
It is an acute multisystem disease, which can affect: 
Cardiovascular: Pericarditis, myocardial infarction and congestive heart failure
Neurological: Seizures, motor, sensory, or mixed sensorimotor polyneuropathy
Gastrointestinal: Abdominal pain, nausea, vomiting, GI infarction
Eyes: Retinal vasculitis, retinal detachment.
Kidneys:  Renal failure
Skin: Rash, purpura, nodules, cutaneous infarcts, Raynaud phenomenon

Investigations

Bloods: FBC, ESR, CRP, ANCA, viral serology, blood cultures
Urine Dip: To screen for infection
Imaging: Chest X-ray or Angiography looking for aneurysms and stenosis
EMG and NCS to assess for peripheral neuropathy

Treatment

Medical: Corticosteroids, cyclophosphamide, anti-viral therapy for hepatitis-
related Polyarteritis Nodosa

Prognosis

Better in patients with cutaneous Polyarteritis Nodosa without systemic or visceral involvement
Cutaneous ulcerations, Extremity gangrene, Organ infarction, Aneurysm rupture, 
Stroke, Heart failure, Myocardial infarction, Pericarditis, Renal failure, Peripheral 
neuropathy, Gastrointestinal bleeding

Key Facts

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Key Images

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Key References

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