Research Evidence
Peer-reviewed studies linked via MeSH term "Polyarteritis Nodosa" from the MEDLINE/PubMed database.
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Clinical characteristics, disease trajectories and management of vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic (VEXAS) syndrome: a systematic review.
[object Object], [object Object], [object Object] et al. · Rheumatol Int · 2024
PMID: 38129348Meta-Analysis
Inflammatory muscle involvement in systemic vasculitis: A systematic review.
[object Object], [object Object], [object Object] et al. · Autoimmun Rev · 2022
PMID: 34971804Meta-Analysis
Systematic review of childhood-onset polyarteritis nodosa and DADA2.
[object Object], [object Object], [object Object] et al. · Semin Arthritis Rheum · 2021
PMID: 33901990Meta-Analysis
Therapeutic options for cutaneous polyarteritis nodosa: a systematic review.
[object Object], [object Object], [object Object] et al. · Rheumatology (Oxford) · 2021
PMID: 33944902Meta-Analysis
Changing etiology and management patterns for spontaneous renal hemorrhage: a systematic review of contemporary series.
[object Object], [object Object], [object Object] et al. · Int Urol Nephrol · 2017
PMID: 28871505Meta-Analysis
Adding Azathioprine to Remission-Induction Glucocorticoids for Eosinophilic Granulomatosis With Polyangiitis (Churg-Strauss), Microscopic Polyangiitis, or Polyarteritis Nodosa Without Poor Prognosis Factors: A Randomized, Controlled Trial.
[object Object], [object Object], [object Object] et al. · Arthritis Rheumatol · 2017
PMID: 28678392RCT
Mononeuritis multiplex predicts the need for immunosuppressive or immunomodulatory drugs for EGPA, PAN and MPA patients without poor-prognosis factors.
[object Object], [object Object], [object Object] et al. · Autoimmun Rev · 2014
PMID: 25153486RCT
Idiopathic polyarteritis nodosa-does it still exist? Viewpoint 2: idiopathic polyarteritis nodosa is rare, but still exists.
[object Object] · Rheumatology (Oxford) · 2025
PMID: 40071408Review
Mimics and challenging presentations of DADA2.
[object Object], [object Object], [object Object] · Clin Exp Immunol · 2025
[Polyarteritis nodosa].
[object Object], [object Object], [object Object] et al. · Rev Prat · 2025
PMID: 41128202Review
Search all PubMed articles for Polyarteritis nodosa
Research data from MEDLINE/PubMed
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormality of skin morphology
Very frequent (80-99%)HP:0011121
Arthralgias
Frequent (30-79%)HP:0002829
Elevated C-reactive protein level
Frequent (30-79%)HP:0011227
Livedo racemosa
Frequent (30-79%)HP:0033260
Muscle pain
Frequent (30-79%)HP:0003326
Peripheral neuropathy
Frequent (30-79%)HP:0009830
Polyarticular arthritis
Frequent (30-79%)HP:0005764
Polyneuritis
Frequent (30-79%)HP:0031003
Pyrexia
Frequent (30-79%)HP:0001945
Renal anomalies
Frequent (30-79%)HP:0000077
Weight loss
Frequent (30-79%)HP:0001824
Abnormality of cardiovascular system morphology
Occasional (5-29%)HP:0030680
Abnormality of the lungs
Occasional (5-29%)HP:0002088
Abnormality of the nervous system
Occasional (5-29%)HP:0000707
Central nervous system disease
Occasional (5-29%)HP:0002011
Cutis marmorata
Occasional (5-29%)HP:0000965
Digestive system disease
Occasional (5-29%)HP:0011024
Erythema
Occasional (5-29%)HP:0010783
High blood pressure
Occasional (5-29%)HP:0000822
Multiple, subcutaneous nodules
Occasional (5-29%)HP:0001482
Open skin sore
Occasional (5-29%)HP:0200042
Raynaud phenomenon
Occasional (5-29%)HP:0030880
Sensory axonal neuropathy
Occasional (5-29%)HP:0003390
Swelling or irritation of membrane around heart
Occasional (5-29%)HP:0001701
Upset stomach
Occasional (5-29%)HP:0002027
Abnormal eye
Very rare (1-4%)HP:0000478
Disease of the heart muscle
Very rare (1-4%)HP:0001638
Pleurisy
Very rare (1-4%)HP:0002102
Quick Facts
- SNOMED CT
- 155441006
- UMLS CUI
- C0031036
- Fully Specified Name
- Polyarteritis nodosa (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 28
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.