Dermatomyositis

A type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness.



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Narrow down the case reports



Total: 1310 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
11
(35.3%)
29707197
(5883386)
Case Report: Clinically amyopathic dermatomyositis presenting acutely with isolated facial edema.
Pappa E, Gkeka M, Protogerou A, Marinos L, Loupa C, Christopoulos C.
F1000Res. 2018;7:60.
Facial edema Muscle weakness
11
(35.3%)
25890241
(4379589)
Dermatomyositis as the first manifestation of gallbladder adenocarcinoma: case report and literature overview.
Jurcic P.
World J Surg Oncol. 2015;13:127.
Proximal muscle weakness Periorbital edema
Adenocarcinoma Dermatomyositis Females Homo sapiens Middle Aged Muscle Weakness Paraneoplastic Syndromes
11
(35.3%)
24156177
Hemophagocytic lymphohistiocytosis associated with dermatomyositis: a case report.
Thomas A, Appiah J, Langsam J, Parker S, Christian C.
Conn Med. 2013;77(8):481-5.
Inflammatory myopathy Periorbital edema
Dermatomyositis Disease Progression Fatal Outcome Homo sapiens Lymphohistiocytosis, Hemophagocytic Male Middle Aged
11
(35.3%)
23930362
Vesiculobullous dermatomyositis with sensory motor neuropathy.
Ayhan E, Baykara SN, Ozekinci S, Aytekin S.
Skinmed. 2013;11(3):185-7.
Muscle weakness Periorbital edema
SSB TRIM21
Biopsy Dermatomyositis Endoscopy, Digestive System Glucocorticoids Homo sapiens Male Peripheral Nervous System Diseases Skin Diseases, Vesiculobullous
11
(35.3%)
22376996
A fatal presentation of dermatomyositis with facial swelling.
Dwivedi N, Michael C, Lew DB, Arnold S, Igarashi M, Bertorini T, Thompson JW, Myers LK, Brown ML.
Int J Pediatr Otorhinolaryngol. 2012;76(5):745-9.
Muscle weakness Periorbital edema
Biopsy Dermatomyositis Edema Face Fatal Outcome Homo sapiens Male
11
(35.3%)
18414893
Anasarca: not a nephrotic syndrome but dermatomyositis.
Zedan M, El-Ayouty M, Abdel-Hady H, Shouman B, El-Assmy M, Fouda A.
Eur J Pediatr. 2008;167(7):831-4.
Facial edema Muscle weakness
Child, Preschool Dermatomyositis Differential Diagnosis Electromyography Homo sapiens Magnetic Resonance Imaging Male Nephrotic Syndrome
11
(35.3%)
17923750
(2694392)
Dermatomyositis associated with cancer of unknown primary site.
Kim HI, Chung SH, Hwang JE, Kim SH, Ahn JS, Yang DH, Kim YK, Yun SJ, Cho SH, Lee JJ, Chung IJ, Kim HJ.
J Korean Med Sci. 2007;22 Suppl:S174-7.
Facial edema Muscle weakness
Dermatomyositis Females Homo sapiens Middle Aged Neoplasms, Unknown Primary
11
(35.3%)
8161622
Dermatomyositis associated with Lyme disease: case report and review of Lyme myositis.
Horowitz HW, Sanghera K, Goldberg N, Pechman D, Kamer R, Duray P, Weinstein A.
Clin Infect Dis. 1994;18(2):166-71.
Proximal muscle weakness Periorbital edema
Anti-Bacterial Agents Dermatomyositis Homo sapiens Lyme Disease Male Middle Aged Muscle Tissue Skin Steroids
11
(35.3%)
7875972
[Pre-myopathic versus amyopathic dermatomyositis. 2 personal cases and review of the literature].
Trautmann C, Abdel-Naser MB, Soehnchen R, Detmar M, Orfanos CE.
Hautarzt. 1995;46(1):47-52.
Periorbital edema Myositis
Adult Dermatomyositis Differential Diagnosis Dose-Response Relationship, Drug Drug Administration Schedule Females Fluorescent Antibody Technique Follow-Up Studies Homo sapiens Male Muscle Tissue Myositis
20
(33.8%)
19374205
[Tumoral calcinosis in a child: a case report and review].
Laswad T, Alamo L, Hofer M, Rotman S, Gudinchet F.
Praxis (Bern 1994). 2009;98(1):23-8.
Calcinosis Large elbow
Antirheumatic Agents Calcinosis Child Dermatomyositis Females Follow-Up Studies Homo sapiens Magnetic Resonance Imaging Male X-Ray Computed Tomography
        

Phenotype(s) retrieved from Orphanet

    Total: 49

HPO ID Term Frequency
HP:0000492 Abnormal eyelid morphology Very frequent (99-80%)
HP:0000969 Edema Very frequent (99-80%)
HP:0002960 Autoimmunity Very frequent (99-80%)
HP:0003326 Myalgia Very frequent (99-80%)
HP:0003457 EMG abnormality Very frequent (99-80%)
HP:0003701 Proximal muscle weakness Very frequent (99-80%)
HP:0009071 Inflammatory myopathy Very frequent (99-80%)
HP:0010783 Erythema Very frequent (99-80%)
HP:0100539 Periorbital edema Very frequent (99-80%)
HP:0000934 Chondrocalcinosis Frequent (79-30%)
HP:0000958 Dry skin Frequent (79-30%)
HP:0000989 Pruritus Frequent (79-30%)
HP:0001063 Acrocyanosis Frequent (79-30%)
HP:0001252 Muscular hypotonia Frequent (79-30%)
HP:0001369 Arthritis Frequent (79-30%)
HP:0001597 Abnormality of the nail Frequent (79-30%)
HP:0001824 Weight loss Frequent (79-30%)
HP:0002093 Respiratory insufficiency Frequent (79-30%)
HP:0002205 Recurrent respiratory infections Frequent (79-30%)
HP:0002206 Pulmonary fibrosis Frequent (79-30%)
HP:0002207 Diffuse reticular or finely nodular infiltrations Frequent (79-30%)
HP:0002829 Arthralgia Frequent (79-30%)
HP:0006530 Interstitial pulmonary abnormality Frequent (79-30%)
HP:0011362 Abnormal hair quantity Frequent (79-30%)
HP:0012378 Fatigue Frequent (79-30%)
HP:0200034 Papule Frequent (79-30%)
HP:0200042 Skin ulcer Frequent (79-30%)
HP:0000992 Cutaneous photosensitivity Occasional (29-5%)
HP:0001608 Abnormality of the voice Occasional (29-5%)
HP:0001618 Dysphonia Occasional (29-5%)
HP:0001658 Myocardial infarction Occasional (29-5%)
HP:0001701 Pericarditis Occasional (29-5%)
HP:0001879 Abnormal eosinophil morphology Occasional (29-5%)
HP:0001945 Fever Occasional (29-5%)
HP:0002092 Pulmonary arterial hypertension Occasional (29-5%)
HP:0002633 Vasculitis Occasional (29-5%)
HP:0002664 Neoplasm Occasional (29-5%)
HP:0002665 Lymphoma Occasional (29-5%)
HP:0003002 Breast carcinoma Occasional (29-5%)
HP:0008065 Aplasia/Hypoplasia of the skin Occasional (29-5%)
HP:0008872 Feeding difficulties in infancy Occasional (29-5%)
HP:0011675 Arrhythmia Occasional (29-5%)
HP:0011703 Sinus tachycardia Occasional (29-5%)
HP:0012819 Myocarditis Occasional (29-5%)
HP:0030078 Lung adenocarcinoma Occasional (29-5%)
HP:0100585 Telangiectasia of the skin Occasional (29-5%)
HP:0100658 Cellulitis Occasional (29-5%)
HP:0100723 Gastrointestinal stroma tumor Occasional (29-5%)
HP:0100758 Gangrene Occasional (29-5%)


Phenotype(s) retrieved from case reports

    Total: 252

HPO ID Term # of case reports
HP:0100614 Myositis 67
HP:0002090 Pneumonia 66
HP:0001370 Rheumatoid arthritis 57
HP:0009071 Inflammatory myopathy 46
HP:0001324 Muscle weakness 39
HP:0025421 Pneumomediastinum 39
HP:0030731 Carcinoma 38
HP:0002861 Melanoma 35
HP:0003761 Calcinosis 35
HP:0003198 Myopathy 34
HP:0010783 Erythema 29
HP:0012490 Panniculitis 29
HP:0003701 Proximal muscle weakness 27
HP:0000988 Skin rash 22
HP:0025508 Gottron's papules 19
HP:0002664 Neoplasm 18
HP:0012115 Hepatitis 18
HP:0040324 Heliotrope rash 16
HP:0000969 Edema 15
HP:0002097 Emphysema 14
HP:0001945 Fever 13
HP:0002015 Dysphagia 13
HP:0002206 Pulmonary fibrosis 13
HP:0025520 Calcinosis cutis 12
HP:0006515 Interstitial pneumonitis 11
HP:0001369 Arthritis 10
HP:0002878 Respiratory failure 10
HP:0000819 Diabetes mellitus 8
HP:0000956 Acanthosis nigricans 8
HP:0001009 Telangiectasia 8
HP:0001019 Erythroderma 8
HP:0030078 Lung adenocarcinoma 8
HP:0200034 Papule 8
HP:0000488 Retinopathy 7
HP:0003003 Colon cancer 7
HP:0005523 Lymphoproliferative disorder 7
HP:0025318 Ovarian carcinoma 7
HP:0000099 Glomerulonephritis 6
HP:0001909 Leukemia 6
HP:0002107 Pneumothorax 6
HP:0002716 Lymphadenopathy 6
HP:0003201 Rhabdomyolysis 6
HP:0025535 Shawl sign 6
HP:0100539 Periorbital edema 6
HP:0100646 Thyroiditis 6
HP:0000822 Hypertension 5
HP:0000989 Pruritus 5
HP:0001025 Urticaria 5
HP:0002860 Squamous cell carcinoma 5
HP:0003326 Myalgia 5
HP:0006740 Transitional cell carcinoma of the bladder 5
HP:0008978 Necrotizing myopathy 5
HP:0032252 Granuloma 5
HP:0100537 Fasciitis 5
HP:0200042 Skin ulcer 5
HP:0000790 Hematuria 4
HP:0000939 Osteoporosis 4
HP:0001029 Poikiloderma 4
HP:0001482 Subcutaneous nodule 4
HP:0001658 Myocardial infarction 4
HP:0001824 Weight loss 4
HP:0002027 Abdominal pain 4
HP:0002094 Dyspnea 4
HP:0002202 Pleural effusion 4
HP:0002955 Granulomatosis 4
HP:0012819 Myocarditis 4
HP:0025615 Abscess 4
HP:0200123 Chronic hepatitis 4
HP:0000100 Nephrotic syndrome 3
HP:0000112 Nephropathy 3
HP:0000821 Hypothyroidism 3
HP:0000979 Purpura 3
HP:0001638 Cardiomyopathy 3
HP:0001873 Thrombocytopenia 3
HP:0002093 Respiratory insufficiency 3
HP:0002102 Pleuritis 3
HP:0002204 Pulmonary embolism 3
HP:0002913 Myoglobinuria 3
HP:0007430 Generalized edema 3
HP:0007618 Subcutaneous calcification 3
HP:0011838 Sclerodactyly 3
HP:0012050 Anasarca 3
HP:0012125 Prostate cancer 3
HP:0012344 Morphea 3
HP:0012378 Fatigue 3
HP:0030357 Small cell lung carcinoma 3
HP:0100279 Ulcerative colitis 3
HP:0100658 Cellulitis 3
HP:0100806 Sepsis 3
HP:0000093 Proteinuria 2
HP:0000155 Oral ulcer 2
HP:0000572 Visual loss 2
HP:0000709 Psychosis 2
HP:0000855 Insulin resistance 2
HP:0001036 Parakeratosis 2
HP:0001051 Seborrheic dermatitis 2
HP:0001250 Seizures 2
HP:0001394 Cirrhosis 2
HP:0001635 Congestive heart failure 2
HP:0001701 Pericarditis 2
HP:0001876 Pancytopenia 2
HP:0001880 Eosinophilia 2
HP:0002024 Malabsorption 2
HP:0002098 Respiratory distress 2
HP:0002588 Duodenal ulcer 2
HP:0002721 Immunodeficiency 2
HP:0002960 Autoimmunity 2
HP:0003040 Arthropathy 2
HP:0003072 Hypercalcemia 2
HP:0003470 Paralysis 2
HP:0009073 Progressive proximal muscle weakness 2
HP:0011974 Myelofibrosis 2
HP:0012126 Stomach cancer 2
HP:0012151 Hemothorax 2
HP:0012722 Heart block 2
HP:0012735 Cough 2
HP:0030394 Fallopian tube carcinoma 2
HP:0031273 Shock 2
HP:0031690 Opportunistic infection 2
HP:0032379 Polymorphous light eruption 2
HP:0100519 Anuria 2
HP:0100584 Endocarditis 2
HP:0100601 Eclampsia 2
HP:0100726 Kaposi's sarcoma 2
HP:0200120 Chronic active hepatitis 2
HP:0000071 Ureteral stenosis 1
HP:0000083 Renal insufficiency 1
HP:0000123 Nephritis 1
HP:0000282 Facial edema 1
HP:0000544 External ophthalmoplegia 1
HP:0000602 Ophthalmoplegia 1
HP:0000621 Entropion 1
HP:0000656 Ectropion 1
HP:0000726 Dementia 1
HP:0000763 Sensory neuropathy 1
HP:0000824 Growth hormone deficiency 1
HP:0000843 Hyperparathyroidism 1
HP:0000964 Eczema 1
HP:0001041 Facial erythema 1
HP:0001047 Atopic dermatitis 1
HP:0001217 Clubbing 1
HP:0001269 Hemiparesis 1
HP:0001271 Polyneuropathy 1
HP:0001279 Syncope 1
HP:0001287 Meningitis 1
HP:0001289 Confusion 1
HP:0001297 Stroke 1
HP:0001513 Obesity 1
HP:0001541 Ascites 1
HP:0001618 Dysphonia 1
HP:0001649 Tachycardia 1
HP:0001698 Pericardial effusion 1
HP:0001733 Pancreatitis 1
HP:0001735 Acute pancreatitis 1
HP:0001878 Hemolytic anemia 1
HP:0001891 Iron deficiency anemia 1
HP:0001903 Anemia 1
HP:0001919 Acute kidney injury 1
HP:0002014 Diarrhea 1
HP:0002017 Nausea and vomiting 1
HP:0002035 Rectal prolapse 1
HP:0002039 Anorexia 1
HP:0002072 Chorea 1
HP:0002099 Asthma 1
HP:0002108 Spontaneous pneumothorax 1
HP:0002113 Pulmonary infiltrates 1
HP:0002140 Ischemic stroke 1
HP:0002155 Hypertriglyceridemia 1
HP:0002176 Spinal cord compression 1
HP:0002240 Hepatomegaly 1
HP:0002315 Headache 1
HP:0002352 Leukoencephalopathy 1
HP:0002411 Myokymia 1
HP:0002563 Constrictive pericarditis 1
HP:0002592 Gastric ulcer 1
HP:0002615 Hypotension 1
HP:0002617 Dilatation 1
HP:0002719 Recurrent infections 1
HP:0002762 Multiple exostoses 1
HP:0002829 Arthralgia 1
HP:0002835 Aspiration 1
HP:0002862 Bladder carcinoma 1
HP:0002863 Myelodysplasia 1
HP:0002905 Hyperphosphatemia 1
HP:0002907 Microscopic hematuria 1
HP:0003095 Septic arthritis 1
HP:0003236 Elevated serum creatine kinase 1
HP:0003690 Limb muscle weakness 1
HP:0004326 Cachexia 1
HP:0004756 Ventricular tachycardia 1
HP:0004942 Aortic aneurysm 1
HP:0005110 Atrial fibrillation 1
HP:0005145 Coronary artery stenosis 1
HP:0005162 Left ventricular dysfunction 1
HP:0005263 Gastritis 1
HP:0005268 Spontaneous abortion 1
HP:0006946 Recurrent meningitis 1
HP:0007178 Motor polyneuropathy 1
HP:0007502 Follicular hyperkeratosis 1
HP:0008682 Acute tubular necrosis 1
HP:0009125 Lipodystrophy 1
HP:0009792 Teratoma 1
HP:0009830 Peripheral neuropathy 1
HP:0009831 Mononeuropathy 1
HP:0010310 Chylothorax 1
HP:0010766 Ectopic calcification 1
HP:0011531 Vitritis 1
HP:0011675 Arrhythmia 1
HP:0011704 Sick sinus syndrome 1
HP:0011951 Aspiration pneumonia 1
HP:0012085 Pyuria 1
HP:0012089 Arteritis 1
HP:0012114 Endometrial carcinoma 1
HP:0012156 Hemophagocytosis 1
HP:0012188 Hyperemesis gravidarum 1
HP:0012226 Ovarian teratoma 1
HP:0012234 Agranulocytosis 1
HP:0012251 ST segment elevation 1
HP:0012315 Histiocytoma 1
HP:0012432 Chronic fatigue 1
HP:0012486 Myelitis 1
HP:0012531 Pain 1
HP:0012578 Membranous nephropathy 1
HP:0012636 Retinal vein occlusion 1
HP:0012733 Macule 1
HP:0025142 Constitutional symptom 1
HP:0025342 Central retinal artery occlusion 1
HP:0025388 Thyroid nodule 1
HP:0025406 Asthenia 1
HP:0025637 Vasospasm 1
HP:0030157 Flank pain 1
HP:0030413 Squamous cell carcinoma of the tongue 1
HP:0030449 Therapeutic abortion 1
HP:0030808 Ragged cuticle 1
HP:0030833 Neck pain 1
HP:0030880 Raynaud phenomenon 1
HP:0031274 Hypovolemic shock 1
HP:0031368 Intestinal perforation 1
HP:0032118 Retinitis 1
HP:0032245 Abnormal metabolism 1
HP:0032282 Contact dermatitis 1
HP:0100295 Muscle fiber atrophy 1
HP:0100550 Tendon rupture 1
HP:0100578 Lipoatrophy 1
HP:0100633 Esophagitis 1
HP:0100644 Melanonychia 1
HP:0100665 Angioedema 1
HP:0100749 Chest pain 1
HP:0100769 Synovitis 1
HP:0100825 Cheilitis 1
HP:0200039 Pustule 1
HP:0200119 Acute hepatitis 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID