Polymyositis

A rare idiopathic inflammatory myopathy characterized by symmetric proximal muscle weakness and elevated muscle enzymes.



Input patient's signs and symptoms


Narrow down the case reports



Total: 1066 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(45.3%)
25808874
A rare case of splenic lymphoma in a patient with polymyositis manifesting as gastric variceal bleeding.
Parekh R, Walia S, Zalawadia A, Siddiqui Y.
Clin J Gastroenterol. 2015;8(2):92-6.
Edema Splenomegaly Melena
Antineoplastic Combined Chemotherapy Protocols Diffuse Large B-Cell Lymphoma Esophageal and Gastric Varices Homo sapiens Male Middle Aged Polymyositis Splenectomy Splenic Neoplasms Splenomegaly Venous Thrombosis
2
(44.7%)
3972708
Sulfadiazine-induced allergy in six Doberman pinschers.
Giger U, Werner LL, Millichamp NJ, Gorman NT.
J Am Vet Med Assoc. 1985;186(5):479-84.
Skin rash Anemia Fever
Animals Arthritis Canis familiaris Combination Drug Therapy Dog Diseases Drug Allergy Glomerulonephritis Retinitis
3
(43.6%)
15492606
Eosinophilic gastroenteritis associated with systemic lupus erythematosus.
Barbie DA, Mangi AA, Lauwers GY.
J Clin Gastroenterol. 2004;38(10):883-6.
Proteinuria Purpura Ascites
Adult Antibodies, Antinuclear Eosinophilia Females Gastroenteritis Glucocorticoids Homo sapiens Intestines, Small Laparoscopy Laparotomy Lupus Erythematosus, Systemic
4
(43.3%)
2880997
Cholestasis and fatal agranulocytosis complicating sulfasalazine therapy: case report and review of the literature.
Mitrane MP, Singh A, Seibold JR.
J Rheumatol. 1986;13(5):969-72.
Jaundice Fever Agranulocytosis
Agranulocytosis Females Homo sapiens Intrahepatic Cholestasis Middle Aged Myositis Rheumatoid Arthritis
5
(41.0%)
18583892
(2526540)
Drug Rash with Eosinophilia and Systemic Symptoms (DRESS) syndrome induced by celecoxib and anti-tuberculosis drugs.
Lee JH, Park HK, Heo J, Kim TO, Kim GH, Kang DH, Song GA, Cho M, Kim DS, Kim HW, Lee CH.
J Korean Med Sci. 2008;23(3):521-5.
Fever Lymphadenopathy Hepatitis Hypereosinophilia
Adult Anti-Inflammatory Agents, Non-Steroidal Antitubercular Agents Arthritis Drug Eruptions Eosinophilia Females Homo sapiens Myositis Pyrazoles Sulfonamides Syndrome Tuberculosis, Pulmonary
6
(38.2%)
17351545
[Fasciitis with eosinophilia: a possible causal role of angiotensin converting enzyme inhibitor].
Serratrice J, Pellissier JF, Champsaur P, Weiller PJ.
Rev Neurol (Paris). 2007;163(2):241-3.
Eosinophilia Angioedema
ACE
Adult Angioedema Angiotensin-Converting Enzyme Inhibitors Drug Eruptions Eosinophilia Fasciitis Females Homo sapiens Obesity
6
(38.2%)
2994360
Disseminated intravascular coagulation induced by generalized cytomegalic inclusion disease during steroid therapy for polymyositis.
Shimizu K, Kishikawa M, Sekine I, Nishimori I, Kawajiri A.
Acta Pathol Jpn. 1985;35(3):723-30.
Purpura Fever
Cytomegalovirus Infections Disseminated Intravascular Coagulation Females Homo sapiens Middle Aged Muscle Tissue Myositis Steroids
6
(38.2%)
1693928
Eosinophilic polymyositis induced by tranilast.
Arase S, Kato S, Nakanishi H, Sadamoto Y, Urano Y, Kawai H, Takeda K.
J Dermatol. 1990;17(3):182-6.
Eosinophilia Erythema Low-grade fever
MB
Asthma Drug Eruptions Eosinophilia Homo sapiens Male Middle Aged Myositis ortho-Aminobenzoates
9
(37.8%)
30874235
Hepatocellular Carcinoma-Associated Polymyositis Presenting With Unilateral Upper Limb Subcutaneous Edema.
Meng-Ko T, Yi-Hsin C, You-Hsin C, Kuo-Lung L.
Arch Rheumatol. 2018;33(4):482-487.
Edema Venous thrombosis Chronic hepatitis
9
(37.8%)
15515704
[Inclusion body myositis after interferon-alpha treatment in a patient with HCV and HTLV-1 infection].
Warabi Y, Matsubara S, Mizutani T, Hayashi H.
Rinsho Shinkeigaku. 2004;44(9):609-14.
Leukemia Elevated serum creatine kinase Hepatitis
IFNA1
HTLV-I Infections Hepatitis C Homo sapiens Interferon-alpha Male Middle Aged Tropical Spastic Paraparesis
        

Phenotype(s) retrieved from Orphanet

    Total: 41

HPO ID Term Frequency
HP:0001252 Muscular hypotonia Very frequent (99-80%)
HP:0002829 Arthralgia Very frequent (99-80%)
HP:0002960 Autoimmunity Very frequent (99-80%)
HP:0003236 Elevated serum creatine kinase Very frequent (99-80%)
HP:0003457 EMG abnormality Very frequent (99-80%)
HP:0003701 Proximal muscle weakness Very frequent (99-80%)
HP:0004303 Abnormal muscle fiber morphology Very frequent (99-80%)
HP:0012544 Elevated aldolase level Very frequent (99-80%)
HP:0012735 Cough Very frequent (99-80%)
HP:0001369 Arthritis Frequent (79-30%)
HP:0001824 Weight loss Frequent (79-30%)
HP:0001945 Fever Frequent (79-30%)
HP:0002019 Constipation Frequent (79-30%)
HP:0002039 Anorexia Frequent (79-30%)
HP:0002093 Respiratory insufficiency Frequent (79-30%)
HP:0002875 Exertional dyspnea Frequent (79-30%)
HP:0003326 Myalgia Frequent (79-30%)
HP:0006530 Interstitial pulmonary abnormality Frequent (79-30%)
HP:0012378 Fatigue Frequent (79-30%)
HP:0000091 Abnormal renal tubule morphology Occasional (29-5%)
HP:0000934 Chondrocalcinosis Occasional (29-5%)
HP:0001288 Gait disturbance Occasional (29-5%)
HP:0001315 Reduced tendon reflexes Occasional (29-5%)
HP:0001608 Abnormality of the voice Occasional (29-5%)
HP:0001618 Dysphonia Occasional (29-5%)
HP:0001633 Abnormal mitral valve morphology Occasional (29-5%)
HP:0001635 Congestive heart failure Occasional (29-5%)
HP:0001639 Hypertrophic cardiomyopathy Occasional (29-5%)
HP:0001644 Dilated cardiomyopathy Occasional (29-5%)
HP:0001658 Myocardial infarction Occasional (29-5%)
HP:0001701 Pericarditis Occasional (29-5%)
HP:0002020 Gastroesophageal reflux Occasional (29-5%)
HP:0002027 Abdominal pain Occasional (29-5%)
HP:0002206 Pulmonary fibrosis Occasional (29-5%)
HP:0002239 Gastrointestinal hemorrhage Occasional (29-5%)
HP:0002240 Hepatomegaly Occasional (29-5%)
HP:0002633 Vasculitis Occasional (29-5%)
HP:0003002 Breast carcinoma Occasional (29-5%)
HP:0004936 Venous thrombosis Occasional (29-5%)
HP:0005150 Abnormal atrioventricular conduction Occasional (29-5%)
HP:0011675 Arrhythmia Occasional (29-5%)


Phenotype(s) retrieved from case reports

    Total: 247

HPO ID Term # of case reports
HP:0003198 Myopathy 58
HP:0100614 Myositis 57
HP:0001370 Rheumatoid arthritis 46
HP:0001324 Muscle weakness 39
HP:0002090 Pneumonia 35
HP:0009071 Inflammatory myopathy 34
HP:0012819 Myocarditis 25
HP:0003701 Proximal muscle weakness 19
HP:0002878 Respiratory failure 15
HP:0012115 Hepatitis 15
HP:0000821 Hypothyroidism 13
HP:0001369 Arthritis 13
HP:0003326 Myalgia 13
HP:0001945 Fever 12
HP:0002206 Pulmonary fibrosis 11
HP:0003201 Rhabdomyolysis 11
HP:0006515 Interstitial pneumonitis 11
HP:0100646 Thyroiditis 11
HP:0001271 Polyneuropathy 10
HP:0002015 Dysphagia 9
HP:0002196 Myelopathy 9
HP:0030731 Carcinoma 9
HP:0000099 Glomerulonephritis 8
HP:0001880 Eosinophilia 8
HP:0001638 Cardiomyopathy 7
HP:0002094 Dyspnea 7
HP:0011675 Arrhythmia 7
HP:0100537 Fasciitis 7
HP:0002664 Neoplasm 6
HP:0000836 Hyperthyroidism 5
HP:0001701 Pericarditis 5
HP:0003003 Colon cancer 5
HP:0003805 Rimmed vacuoles 5
HP:0009830 Peripheral neuropathy 5
HP:0025421 Pneumomediastinum 5
HP:0025615 Abscess 5
HP:0000822 Hypertension 4
HP:0000988 Skin rash 4
HP:0001649 Tachycardia 4
HP:0001909 Leukemia 4
HP:0002913 Myoglobinuria 4
HP:0008978 Necrotizing myopathy 4
HP:0012490 Panniculitis 4
HP:0100279 Ulcerative colitis 4
HP:0200120 Chronic active hepatitis 4
HP:0200123 Chronic hepatitis 4
HP:0000093 Proteinuria 3
HP:0000112 Nephropathy 3
HP:0000969 Edema 3
HP:0000979 Purpura 3
HP:0001297 Stroke 3
HP:0001635 Congestive heart failure 3
HP:0001658 Myocardial infarction 3
HP:0001824 Weight loss 3
HP:0002098 Respiratory distress 3
HP:0002202 Pleural effusion 3
HP:0002721 Immunodeficiency 3
HP:0003040 Arthropathy 3
HP:0004308 Ventricular arrhythmia 3
HP:0008942 Acute rhabdomyolysis 3
HP:0012344 Morphea 3
HP:0012722 Heart block 3
HP:0100769 Synovitis 3
HP:0000100 Nephrotic syndrome 2
HP:0000819 Diabetes mellitus 2
HP:0001287 Meningitis 2
HP:0001300 Parkinsonism 2
HP:0001698 Pericardial effusion 2
HP:0001919 Acute kidney injury 2
HP:0001954 Recurrent fever 2
HP:0002014 Diarrhea 2
HP:0002093 Respiratory insufficiency 2
HP:0002315 Headache 2
HP:0002860 Squamous cell carcinoma 2
HP:0002861 Melanoma 2
HP:0002900 Hypokalemia 2
HP:0003002 Breast carcinoma 2
HP:0003072 Hypercalcemia 2
HP:0003690 Limb muscle weakness 2
HP:0003713 Muscle fiber necrosis 2
HP:0003761 Calcinosis 2
HP:0004756 Ventricular tachycardia 2
HP:0005523 Lymphoproliferative disorder 2
HP:0006562 Viral hepatitis 2
HP:0006725 Pancreatic adenocarcinoma 2
HP:0009073 Progressive proximal muscle weakness 2
HP:0009831 Mononeuropathy 2
HP:0011641 Coronary artery fistula 2
HP:0011838 Sclerodactyly 2
HP:0011951 Aspiration pneumonia 2
HP:0012089 Arteritis 2
HP:0012251 ST segment elevation 2
HP:0012378 Fatigue 2
HP:0012424 Chorioretinitis 2
HP:0012486 Myelitis 2
HP:0012531 Pain 2
HP:0012578 Membranous nephropathy 2
HP:0012593 Nephrotic range proteinuria 2
HP:0012735 Cough 2
HP:0025318 Ovarian carcinoma 2
HP:0030078 Lung adenocarcinoma 2
HP:0030149 Cardiogenic shock 2
HP:0031003 Polyneuritis 2
HP:0032118 Retinitis 2
HP:0032204 Chronic active Epstein-Barr virus infection 2
HP:0040276 Adenocarcinoma of the colon 2
HP:0100534 Episcleritis 2
HP:0100595 Camptocormia 2
HP:0100653 Optic neuritis 2
HP:0100749 Chest pain 2
HP:0100778 Cryoglobulinemia 2
HP:0100827 Lymphocytosis 2
HP:0000083 Renal insufficiency 1
HP:0000123 Nephritis 1
HP:0000217 Xerostomia 1
HP:0000282 Facial edema 1
HP:0000467 Neck muscle weakness 1
HP:0000488 Retinopathy 1
HP:0000518 Cataract 1
HP:0000541 Retinal detachment 1
HP:0000726 Dementia 1
HP:0000746 Delusions 1
HP:0000829 Hypoparathyroidism 1
HP:0000952 Jaundice 1
HP:0000989 Pruritus 1
HP:0001009 Telangiectasia 1
HP:0001019 Erythroderma 1
HP:0001045 Vitiligo 1
HP:0001217 Clubbing 1
HP:0001250 Seizures 1
HP:0001279 Syncope 1
HP:0001283 Bulbar palsy 1
HP:0001288 Gait disturbance 1
HP:0001289 Confusion 1
HP:0001290 Generalized hypotonia 1
HP:0001298 Encephalopathy 1
HP:0001332 Dystonia 1
HP:0001394 Cirrhosis 1
HP:0001396 Cholestasis 1
HP:0001406 Intrahepatic cholestasis 1
HP:0001433 Hepatosplenomegaly 1
HP:0001541 Ascites 1
HP:0001605 Vocal cord paralysis 1
HP:0001618 Dysphonia 1
HP:0001662 Bradycardia 1
HP:0001677 Coronary artery atherosclerosis 1
HP:0001681 Angina pectoris 1
HP:0001685 Myocardial fibrosis 1
HP:0001700 Myocardial necrosis 1
HP:0001873 Thrombocytopenia 1
HP:0001878 Hemolytic anemia 1
HP:0001882 Leukopenia 1
HP:0001903 Anemia 1
HP:0001907 Thromboembolism 1
HP:0001943 Hypoglycemia 1
HP:0002013 Vomiting 1
HP:0002024 Malabsorption 1
HP:0002027 Abdominal pain 1
HP:0002047 Malignant hyperthermia 1
HP:0002063 Rigidity 1
HP:0002102 Pleuritis 1
HP:0002108 Spontaneous pneumothorax 1
HP:0002110 Bronchiectasis 1
HP:0002113 Pulmonary infiltrates 1
HP:0002204 Pulmonary embolism 1
HP:0002249 Melena 1
HP:0002385 Paraparesis 1
HP:0002563 Constrictive pericarditis 1
HP:0002583 Colitis 1
HP:0002617 Dilatation 1
HP:0002666 Pheochromocytoma 1
HP:0002716 Lymphadenopathy 1
HP:0002749 Osteomalacia 1
HP:0002754 Osteomyelitis 1
HP:0002791 Hypoventilation 1
HP:0002829 Arthralgia 1
HP:0002835 Aspiration 1
HP:0002863 Myelodysplasia 1
HP:0002955 Granulomatosis 1
HP:0002960 Autoimmunity 1
HP:0003095 Septic arthritis 1
HP:0003128 Lactic acidosis 1
HP:0003259 Elevated serum creatinine 1
HP:0003324 Generalized muscle weakness 1
HP:0003434 Sensory ataxic neuropathy 1
HP:0003457 EMG abnormality 1
HP:0003546 Exercise intolerance 1
HP:0003722 Neck flexor weakness 1
HP:0003798 Nemaline bodies 1
HP:0004322 Short stature 1
HP:0004389 Intestinal pseudo-obstruction 1
HP:0004755 Supraventricular tachycardia 1
HP:0005294 Arterial dissection 1
HP:0005521 Disseminated intravascular coagulation 1
HP:0005526 Lymphoid leukemia 1
HP:0006682 Ventricular extrasystoles 1
HP:0006824 Cranial nerve paralysis 1
HP:0007430 Generalized edema 1
HP:0008200 Primary hyperparathyroidism 1
HP:0009113 Diaphragmatic weakness 1
HP:0010628 Facial palsy 1
HP:0010783 Erythema 1
HP:0011096 Peripheral demyelination 1
HP:0011134 Low-grade fever 1
HP:0011355 Localized skin lesion 1
HP:0011712 Right bundle branch block 1
HP:0011713 Left bundle branch block 1
HP:0011736 Primary hyperaldosteronism 1
HP:0012074 Tonic pupil 1
HP:0012108 Open angle glaucoma 1
HP:0012125 Prostate cancer 1
HP:0012199 Cluster headache 1
HP:0012219 Erythema nodosum 1
HP:0012234 Agranulocytosis 1
HP:0012315 Histiocytoma 1
HP:0012387 Bronchitis 1
HP:0012473 Tongue atrophy 1
HP:0025044 Lung abscess 1
HP:0025343 Lupus anticoagulant 1
HP:0025477 Periarticular calcification 1
HP:0030834 Shoulder pain 1
HP:0030955 Alcoholism 1
HP:0031002 Neuritis 1
HP:0031047 Paraproteinemia 1
HP:0031273 Shock 1
HP:0031292 Cutaneous abscess 1
HP:0031563 Coronary arteriovenous fistula 1
HP:0031690 Opportunistic infection 1
HP:0032018 Multiple mononeuropathy 1
HP:0032252 Granuloma 1
HP:0032323 Periodic fever 1
HP:0032446 Pulmonary bulla 1
HP:0040075 Hypopituitarism 1
HP:0040165 Periostitis 1
HP:0045073 Serositis 1
HP:0100242 Sarcoma 1
HP:0100519 Anuria 1
HP:0100532 Scleritis 1
HP:0100570 Carcinoid tumor 1
HP:0100584 Endocarditis 1
HP:0100601 Eclampsia 1
HP:0100658 Cellulitis 1
HP:0100721 Mediastinal lymphadenopathy 1
HP:0100726 Kaposi's sarcoma 1
HP:0100806 Sepsis 1
HP:0100820 Glomerulopathy 1
HP:0200119 Acute hepatitis 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID