Amyopathic dermatomyositis
Paget’s Disease of the Breast in a Patient with Amyopathic Dermatomyositis
... in homogeneous pattern; but extractable nuclear antigens (ENA) profile including Anti-Jo-1 and Anti-Mi-2 was neg- ative. Her muscle activity during electromyography (EMG) monitoring was also within normal limits. The ...
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A Case of Polymyxin b-Immobilized Fiber Column Treatment for Rapidly Progressive Interstitial Pneumonia Associated with Clinically Amyopathic Dermatomyositis
... clinically amyopathic dermatomyositis who responded to single course of polymyxin b-immobilized fiber column ...clinically amyopathic dermatomyositis, especially at the early phase of ...
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Epidemiologic study of clinically amyopathic dermatomyositis and anti melanoma differentiation associated gene 5 antibodies in central Japan
... Introduction: Several reports have found the onset or activity of inflammatory myopathies to show spatial clustering and seasonal association. We recently detected autoantibodies against melanoma differentiation- ...
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Clinical effects of direct hemoperfusion using a polymyxin B-immobilized fiber column in clinically amyopathic dermatomyositis-associated rapidly progressive interstitial pneumonias
... Clinically amyopathic dermatomyositis; DIC: Disseminated intravascular coagulation; HMGB-1: High-mobility group box protein 1; HRCT: High-resolution computed tomography; ILD: Interstitial lung disease; IPF: ...
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Amyopathic Dermatomyositis (Anti-MDA 5 disease) with pulmonary fibrosis and features of lupus, without evidence of malignancy: A Case Report
... Amyopathic Dermatomyositis (ADM) also known as dermatomyositis sine myositis, is a distinct subclass of dermatomyositis, distinguished by the classic findings of palmar papules, cutaneous ...
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Acute lyme infection presenting with amyopathic dermatomyositis and rapidly fatal interstitial pulmonary fibrosis: a case report
... to amyopathic dermatomyo- sitis in this case, which is possible, is that early corticos- teroid therapy for COPD stymied the emergence of clinical ...pathic dermatomyositis without clinical myositis still ...
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Nursing Care of Skin Damage of Elbow Gottron’s Disease in a Case of Amyopathic Dermatomyositis Based on Multidisciplinary Cooperation
... Multidisciplinary collaboration should be widely used in patients with rheumatism. Amyopathic dermatomyositis has typical skin lesions, and most of them appeared at rubbed joints. During the active stage of ...
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Correlation between disease activity and serum ferritin in clinically amyopathic dermatomyositis with rapidly progressive interstitial lung disease: a case report
... clinically amyopathic dermatomyositis (CADM) with anti-Melanoma Differentiation-Associated gene 5 (MDA5) antibody often develop treatment-resist- ant, and rapidly-progressive interstitial lung disease (RP- ...
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Myositis autoantibodies in Korean patients with inflammatory myositis: Anti 140 kDa polypeptide antibody is primarily associated with rapidly progressive interstitial lung disease independent of clinically amyopathic dermatomyositis
... and dermatomyositis (DM) are systemic autoimmune diseases in which muscles are the primary target of immune-mediated ...hand, amyopathic dermatomyositis (ADM) is a condition in which the typical skin ...
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Interstitial lung disease in clinically amyopathic dermatomyositis with and without anti-MDA-5 antibody: to lump or split?
... As a background to the differences in the KL-6 and SP-D levels, we believe that immune reactions may differ in the lung between the two groups. The following two results support this sup[r] ...
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Circulating plasma microRNA profiling in patients with polymyositis/dermatomyositis before and after treatment: miRNA may be associated with polymyositis/dermatomyositis
... in keratinocytes led to upregulation of the PKCε protein and resulted in abnormally increased cell proliferation. The serum hsa-miR-223 concentration was decreased in PM/DM patients, particularly in CADM (clinically ...
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Elevated α-defensin levels in plasma and bronchoalveolar lavage fluid from patients with myositis-associated interstitial lung disease
... Clinically amyopathic dermatomyositis; DM: Dermatomyositis; FDR: False-discovery rate; HNPs: Human neutrophil peptides; HRCT: High- resolution computed tomography; IIMs: Idiopathic inflammatory ...
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Anti PM/Scl antibodies are found in Japanese patients with various systemic autoimmune conditions besides myositis and scleroderma
... clinically amyopathic dermatomyositis; CIE: counter immunoelectrophoresis; DM: dermatomyositis; ELISA: enzyme- linked immunosorbent assay; EULAR: European League Against Rheumatism; ID: ...
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Juvenile Dermatomyositis: An Update
... Juvenile dermatomyositis (JDM) is the most common paediatric inflammatory ...polymyositis, amyopathic dermatomyositis, overlap myositis and inclusion body myositis 1 ...
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Being on the Juvenile Dermatomyositis Rollercoaster: a qualitative study
... Juvenile Dermatomyositis is a rare condition typically managed in specialist centres around the world. The physical effects of JDM are often presented in the litera- ture [4, 38–40], but this study brings ...
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Childhood Dermatomyositis: Serial Microvascular Studies
... evolved during several months to the characteristic capillary pattern of childhood dermatomyositis, ie, giant capillary loops and “bushy” capillary forma-.. tions.[r] ...
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Association of nailfold capillary changes with disease activity, clinical and laboratory findings in patients with dermatomyositis
... sides, the classic muscular manifestation is slowly progressive proximal muscle weak- ness. The patients suffering from DM com- plain about difficulties in climbing up the steps, arising from chair, or combing and ...
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The aerobic capacity in patients with antisynthetase syndrome and dermatomyositis
... DM: Dermatomyositis; EULAR: European League Against Rheumatism; HAQ: Health Assessment Questionnaire; ILD: Interstitial lung disease; IMACS: International Myositis Assessment & Clinical Studies Group; MMT: ...
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Juvenile dermatomyositis: is periodontal disease associated with dyslipidemia?
... Gengivitis and/or periodontitis have been seldom studied in pediatric autoimmune diseases, like juvenile idiopathic arthritis and juvenile systemic lupus erythematosus [10 – 15] Recently[r] ...
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Familial Aggregation of Autoimmune Disease in Juvenile Dermatomyositis
... sclerosis, dermatomyositis, sclero- derma, myasthenia gravis, vasculitis, and polymyositis were all very close to the reported population rates would suggest that these estimates are accu- ...
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