Polyarteritis nodosa

Polyarteritis nodosa (PAN) is a rare, clinically heterogeneous, rheumatologic disease characterized by necrotizing inflammatory lesions affecting small- and medium-sized blood vessels. PAN most commonly affects skin, joints, peripheral nerves, the gut, and the kidney.



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Narrow down the case reports



Total: 901 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(56.2%)
1688204
[Menetrier's hypertrophic gastritis associated with polyarteritis nodosa].
Nigro DR, Freytes Santamarina AG, David JF.
Rev Fac Cien Med Univ Nac Cordoba. 1991;49(2):19-22.
Edema Splenomegaly Anemia
Differential Diagnosis Gastritis, Hypertrophic Homo sapiens Male Middle Aged Polyarteritis Nodosa
2
(51.2%)
12688329
Idiopathic myelofibrosis associated with classic polyarteritis nodosa.
Camos M, Arellano-Rodrigo E, Abello D, Muntanola A, Ferrer A, Grau JM, Cervantes F.
Leuk Lymphoma. 2003;44(3):539-41.
Anemia Fever Abdominal pain Poikilocytosis Raynaud phenomenon
Abdominal Pain Autoimmune Diseases Diagnostic Errors Fatal Outcome Females Homo sapiens Immunosuppressive Agents Middle Aged Polyarteritis Nodosa Primary Myelofibrosis Raynaud Disease Splenic Infarction Splenomegaly Systemic Scleroderma
3
(46.6%)
14712330
A case of familial Mediterranean fever and polyarteritis nodosa complicated by spontaneous perirenal and subcapsular hepatic hemorrhage requiring multiple arterial embolizations.
Akar S, Goktay Y, Akinci B, Tekis D, Biberoglu K, Birlik M, Onen F, Tunca M, Akkoc N.
Rheumatol Int. 2005;25(1):60-4.
Pallor Anemia Abdominal pain Hypoalbuminemia
MEFV
Adult Combination Drug Therapy Embolization, Therapeutic Familial Mediterranean Fever Fatal Outcome Hemorrhage Homo sapiens Kidney Diseases Male Polyarteritis Nodosa
4
(46.2%)
30377239
Renal Amyloidosis in Deficiency of Adenosine Deaminase 2: Successful Experience With Canakinumab.
Kisla Ekinci RM, Balci S, Bisgin A, Hershfield M, Atmis B, Dogruel D, Yilmaz M.
Pediatrics. 2018;142(5):.
Proteinuria Hepatosplenomegaly Splenomegaly Pancytopenia
ADA2
c|DEL|950-950|C p|FS|T|317|R|25 p|SUB|M|694|V
Amyloidosis Antibodies, Monoclonal, Humanized Females High-Throughput Nucleotide Sequencing Homo sapiens Intercellular Signaling Peptides and Proteins Kidney Diseases Monoclonal Antibodies Mutation Severe Combined Immunodeficiency
5
(45.3%)
27799976
Association of Macrophage Activating Syndrome with Castleman's Syndrome in Systemic Lupus Erythematosus.
Shariatpanahi S, Pourfarzam S, Gheini M.
Iran J Pathol. 2016;11(3):265-271.
Edema Splenomegaly Pancytopenia
6
(44.4%)
29391272
Identification of co-occurrence in a patient with Dent's disease and ADA2-deficiency by exome sequencing.
Gunthner R, Wagner M, Thurm T, Ponsel S, Hofele J, Lange-Sperandio B.
Gene. 2018;649:23-26.
Proteinuria Stroke Anemia Abdominal pain
ADA2 CLCN5 CRP
p|SUB|G|47|A;RS#:200930463 p|SUB|P|251|L;RS#:148936893
Adaptor Proteins, Signal Transducing Child, Preschool Chloride Channels Comorbidity DNA-Binding Proteins Exome Homo sapiens Hypercalciuria Intercellular Signaling Peptides and Proteins Kidney Male Mutation Phenotype Whole Exome Sequencing
6
(44.4%)
16765711
Catastrophic Kawasaki disease or juvenile Polyarteritis nodosa?
Yamazaki-Nakashimada MA, Espinosa-Lopez M, Hernandez-Bautista V, Espinosa-Padilla S, Espinosa-Rosales F.
Semin Arthritis Rheum. 2006;35(6):349-54.
Conjunctivitis Anemia Fever Abdominal pain
CRP
Child, Preschool Differential Diagnosis Females Homo sapiens Mucocutaneous Lymph Node Syndrome Polyarteritis Nodosa Severity of Illness Index Vasculitis
8
(43.7%)
18974626
[Gastrointestinal involvement and renal infarction in a boy with classic polyarteritis nodosa diagnosed with 3D-computed tomography angiography].
Sano F, Miyamae T, Nakagishi Y, Kinoshita J, Ozawa R, Imagawa T, Mori M, Asayama M, Yokota S.
Nihon Rinsho Meneki Gakkai Kaishi. 2008;31(5):415-21.
Anemia Fever Abdominal pain
B2M CRP
Gastrointestinal Diseases Homo sapiens Imaging, Three-Dimensional Infarction Kidney Male Polyarteritis Nodosa X-Ray Computed Tomography
8
(43.7%)
12852508
Bilateral renal rupture in a patient on hemodialysis.
Carlson CC, Holsten SJ, Grandas OH.
Am Surg. 2003;69(6):505-7.
Hematuria Anemia Abdominal pain
Cystic Kidney Diseases Hemorrhage Homo sapiens Male Middle Aged Nephrectomy Renal Dialysis Retroperitoneal Space Rupture, Spontaneous
8
(43.7%)
9366170
[Microscopic polyangiitis and pulmonary fibrosis in a patient who died of Candida pneumonia and intra-alveolar hemorrhage].
Kishikawa H, Tojima H, Tokudome T.
Nihon Kyobu Shikkan Gakkai Zasshi. 1997;35(8):915-20.
Proteinuria Anemia Malnutrition
MPO
Candidiasis Fatal Outcome Glomerulonephritis Hemorrhage Homo sapiens Lung Diseases, Fungal Male Polyarteritis Nodosa Pulmonary Fibrosis
        

Phenotype(s) retrieved from Orphanet

    Total: 26

HPO ID Term Frequency
HP:0011121 Abnormality of skin morphology Very frequent (99-80%)
HP:0000077 Abnormality of the kidney Frequent (79-30%)
HP:0001824 Weight loss Frequent (79-30%)
HP:0001945 Fever Frequent (79-30%)
HP:0002829 Arthralgia Frequent (79-30%)
HP:0003326 Myalgia Frequent (79-30%)
HP:0009830 Peripheral neuropathy Frequent (79-30%)
HP:0011227 Elevated C-reactive protein level Frequent (79-30%)
HP:0031003 Polyneuritis Frequent (79-30%)
HP:0000707 Abnormality of the nervous system Occasional (29-5%)
HP:0000822 Hypertension Occasional (29-5%)
HP:0000965 Cutis marmorata Occasional (29-5%)
HP:0001482 Subcutaneous nodule Occasional (29-5%)
HP:0001701 Pericarditis Occasional (29-5%)
HP:0002011 Morphological abnormality of the central nervous system Occasional (29-5%)
HP:0002027 Abdominal pain Occasional (29-5%)
HP:0002088 Abnormal lung morphology Occasional (29-5%)
HP:0003390 Sensory axonal neuropathy Occasional (29-5%)
HP:0010783 Erythema Occasional (29-5%)
HP:0011024 Abnormality of the gastrointestinal tract Occasional (29-5%)
HP:0030680 Abnormality of cardiovascular system morphology Occasional (29-5%)
HP:0030880 Raynaud phenomenon Occasional (29-5%)
HP:0200042 Skin ulcer Occasional (29-5%)
HP:0000478 Abnormality of the eye Very rare (4-1%)
HP:0001638 Cardiomyopathy Very rare (4-1%)
HP:0002102 Pleuritis Very rare (4-1%)


Phenotype(s) retrieved from case reports

    Total: 185

HPO ID Term # of case reports
HP:0012115 Hepatitis 65
HP:0002955 Granulomatosis 43
HP:0012089 Arteritis 33
HP:0000822 Hypertension 26
HP:0000979 Purpura 20
HP:0001370 Rheumatoid arthritis 17
HP:0002027 Abdominal pain 12
HP:0000099 Glomerulonephritis 11
HP:0001945 Fever 11
HP:0002090 Pneumonia 10
HP:0003326 Myalgia 10
HP:0030171 Perirenal hematoma 10
HP:0001880 Eosinophilia 9
HP:0001909 Leukemia 9
HP:0001297 Stroke 7
HP:0012219 Erythema nodosum 7
HP:0030731 Carcinoma 7
HP:0001082 Cholecystitis 6
HP:0001658 Myocardial infarction 6
HP:0002099 Asthma 6
HP:0002621 Atherosclerosis 6
HP:0002721 Immunodeficiency 6
HP:0009830 Peripheral neuropathy 6
HP:0001138 Optic neuropathy 5
HP:0001298 Encephalopathy 5
HP:0001733 Pancreatitis 5
HP:0002617 Dilatation 5
HP:0002829 Arthralgia 5
HP:0012224 Circulating immune complexes 5
HP:0032252 Granuloma 5
HP:0100758 Gangrene 5
HP:0100778 Cryoglobulinemia 5
HP:0200123 Chronic hepatitis 5
HP:0000083 Renal insufficiency 4
HP:0001271 Polyneuropathy 4
HP:0001824 Weight loss 4
HP:0002664 Neoplasm 4
HP:0005206 Pancreatic pseudocyst 4
HP:0009831 Mononeuropathy 4
HP:0025342 Central retinal artery occlusion 4
HP:0040223 Pulmonary hemorrhage 4
HP:0100279 Ulcerative colitis 4
HP:0000031 Epididymitis 3
HP:0000123 Nephritis 3
HP:0000388 Otitis media 3
HP:0001250 Seizures 3
HP:0001482 Subcutaneous nodule 3
HP:0002583 Colitis 3
HP:0004387 Enterocolitis 3
HP:0006000 Ureteral obstruction 3
HP:0010783 Erythema 3
HP:0012578 Membranous nephropathy 3
HP:0030882 Coronary artery aneurysm 3
HP:0100762 Hemobilia 3
HP:0100796 Orchitis 3
HP:0000112 Nephropathy 2
HP:0000126 Hydronephrosis 2
HP:0000491 Keratitis 2
HP:0000651 Diplopia 2
HP:0000793 Membranoproliferative glomerulonephritis 2
HP:0000969 Edema 2
HP:0001025 Urticaria 2
HP:0001287 Meningitis 2
HP:0001394 Cirrhosis 2
HP:0001878 Hemolytic anemia 2
HP:0001894 Thrombocytosis 2
HP:0001919 Acute kidney injury 2
HP:0002138 Subarachnoid hemorrhage 2
HP:0002170 Intracranial hemorrhage 2
HP:0002239 Gastrointestinal hemorrhage 2
HP:0002634 Arteriosclerosis 2
HP:0002716 Lymphadenopathy 2
HP:0005200 Retroperitoneal fibrosis 2
HP:0006859 Posterior leukoencephalopathy 2
HP:0010788 Testicular neoplasm 2
HP:0011946 Bronchiolitis obliterans 2
HP:0012223 Splenic rupture 2
HP:0012490 Panniculitis 2
HP:0012819 Myocarditis 2
HP:0031273 Shock 2
HP:0031368 Intestinal perforation 2
HP:0100532 Scleritis 2
HP:0100584 Endocarditis 2
HP:0100699 Scarring 2
HP:0100817 Renovascular hypertension 2
HP:0200119 Acute hepatitis 2
HP:0000093 Proteinuria 1
HP:0000100 Nephrotic syndrome 1
HP:0000362 Otosclerosis 1
HP:0000365 Hearing impairment 1
HP:0000572 Visual loss 1
HP:0000602 Ophthalmoplegia 1
HP:0000618 Blindness 1
HP:0000648 Optic atrophy 1
HP:0000709 Psychosis 1
HP:0000989 Pruritus 1
HP:0001047 Atopic dermatitis 1
HP:0001101 Iritis 1
HP:0001123 Visual field defect 1
HP:0001279 Syncope 1
HP:0001288 Gait disturbance 1
HP:0001324 Muscle weakness 1
HP:0001342 Cerebral hemorrhage 1
HP:0001369 Arthritis 1
HP:0001635 Congestive heart failure 1
HP:0001638 Cardiomyopathy 1
HP:0001698 Pericardial effusion 1
HP:0001735 Acute pancreatitis 1
HP:0001744 Splenomegaly 1
HP:0001955 Unexplained fevers 1
HP:0002014 Diarrhea 1
HP:0002113 Pulmonary infiltrates 1
HP:0002157 Azotemia 1
HP:0002176 Spinal cord compression 1
HP:0002206 Pulmonary fibrosis 1
HP:0002315 Headache 1
HP:0002317 Unsteady gait 1
HP:0002321 Vertigo 1
HP:0002584 Intestinal bleeding 1
HP:0002592 Gastric ulcer 1
HP:0002647 Aortic dissection 1
HP:0002719 Recurrent infections 1
HP:0002860 Squamous cell carcinoma 1
HP:0002907 Microscopic hematuria 1
HP:0002960 Autoimmunity 1
HP:0003095 Septic arthritis 1
HP:0003193 Allergic rhinitis 1
HP:0004415 Pulmonary artery stenosis 1
HP:0004417 Intermittent claudication 1
HP:0004418 Thrombophlebitis 1
HP:0004469 Chronic bronchitis 1
HP:0004942 Aortic aneurysm 1
HP:0005112 Abdominal aortic aneurysm 1
HP:0005263 Gastritis 1
HP:0005521 Disseminated intravascular coagulation 1
HP:0006562 Viral hepatitis 1
HP:0006689 Bacterial endocarditis 1
HP:0006702 Coronary artery dissection 1
HP:0007178 Motor polyneuropathy 1
HP:0008682 Acute tubular necrosis 1
HP:0009071 Inflammatory myopathy 1
HP:0009900 Unilateral deafness 1
HP:0011134 Low-grade fever 1
HP:0011531 Vitritis 1
HP:0011672 Cardiac myxoma 1
HP:0012032 Lipoma 1
HP:0012074 Tonic pupil 1
HP:0012330 Pyelonephritis 1
HP:0012344 Morphea 1
HP:0012378 Fatigue 1
HP:0012592 Albuminuria 1
HP:0012593 Nephrotic range proteinuria 1
HP:0012849 Small intestinal bleeding 1
HP:0020071 Viremia 1
HP:0025142 Constitutional symptom 1
HP:0025343 Lupus anticoagulant 1
HP:0025497 Coronary artery spasm 1
HP:0025615 Abscess 1
HP:0030151 Cholangitis 1
HP:0030155 Scrotal pain 1
HP:0030164 Jaw claudication 1
HP:0030360 Large cell lung carcinoma 1
HP:0030773 Internuclear ophthalmoplegia 1
HP:0031370 Small intestinal perforation 1
HP:0031625 Pseudoaneurysm 1
HP:0032061 Hypereosinophilia 1
HP:0032169 Severe infection 1
HP:0032323 Periodic fever 1
HP:0032325 Lacunar stroke 1
HP:0032404 Testicular mass 1
HP:0040165 Periostitis 1
HP:0100242 Sarcoma 1
HP:0100519 Anuria 1
HP:0100534 Episcleritis 1
HP:0100545 Arterial stenosis 1
HP:0100653 Optic neuritis 1
HP:0100726 Kaposi's sarcoma 1
HP:0100735 Hypertensive crisis 1
HP:0100749 Chest pain 1
HP:0100806 Sepsis 1
HP:0100809 Scalp tenderness 1
HP:0100813 Testicular torsion 1
HP:0200034 Papule 1
HP:0200084 Giant cell hepatitis 1
HP:0410323 Drug allergy 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID