Dermatomyositis
Identifieur interne : 002828 ( Main/Exploration ); précédent : 002827; suivant : 002829Dermatomyositis
Auteurs : Stephen O. Kovacs [États-Unis] ; S. Christine Kovacs [États-Unis]Source :
- Journal of the American Academy of Dermatology [ 0190-9622 ] ; 1998.
English descriptors
- Teeft :
- Acad, Acad dermatol, American academy, Amyopathic, Amyopathic dermatomyositis, Arthritis, Arthritis rheum, Autoantibody, Azathioprine, Calcinosis, Calcinosis cutis, Callen, Clin, Connective tissue disease, Corticosteroid, Creatine, Curr, Cutaneous, Cutis, Cyclophosphamide, Dalakas, December, Dermatol, Dermatology, Dermatology december, Dermatology volume, Dermatomyositis, Engel, Engl, Erythematosus, Histopathologic, Hydroxychloroquine, Idiopathic, Immunoglobulin, Inflammatory, Inflammatory myopathies, Inflammatory myopathy, Intravenous, Juvenile dermatomyositis, Kovacs, Lancet, Lupus, Lymphocyte, Malignancy, Medsger, Methotrexate, Muscle weakness, Myalgia, Myopathy, Myositis, Neurol, Opin, Pachman, Pathol, Pediatr, Periorbital, Polymyositis, Rash, Rheum, Rheumatoid, Rheumatol, Scleroderma, Skin manifestations, Steroid, Syndrome, Synthetase, Systemic lupus erythematosus, Targoff.
Abstract
Abstract: Dermatomyositis is a rare inflammatory myopathy with characteristic skin manifestations and muscular weakness. The disease can be categorized as adult idiopathic, juvenile, or amyopathic dermatomyositis as well as that associated with a connective tissue disease or a malignancy. Immunologic factors are most likely involved in the pathogenesis of the disease; however, genetic and environmental issues may also play important roles. Treatment with immunosuppressive agents has proved successful in the majority of patients, although significant morbidity still occurs. (J Am Acad Dermatol 1998;39:899-920.) Learning Objective: At the conclusion of this learning activity, participants should be familiar with the clinical characteristics of adult idiopathic, juvenile, and amyopathic dermatomyositis as well as the histopathologic and immunopathologic characteristics of the disease.
Url:
DOI: 10.1016/S0190-9622(98)70263-4
Affiliations:
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Kovacs</name><affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country><placeName><region type="state">État de New York</region></placeName><wicri:cityArea>Laser and Skin Surgery Center of New York New York</wicri:cityArea></affiliation></author><author><name sortKey="Kovacs, S Christine" sort="Kovacs, S Christine" uniqKey="Kovacs S" first="S. Christine" last="Kovacs">S. Christine Kovacs</name><affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country><placeName><region type="state">État de New York</region></placeName><wicri:cityArea>St Vincent’s Hospital. New York</wicri:cityArea></affiliation></author></analytic><monogr></monogr><series><title level="j">Journal of the American Academy of Dermatology</title><title level="j" type="abbrev">YMJD</title><idno type="ISSN">0190-9622</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1998">1998</date><biblScope unit="volume">39</biblScope><biblScope unit="issue">6</biblScope><biblScope unit="page" from="899">899</biblScope><biblScope unit="page" to="922">922</biblScope></imprint><idno type="ISSN">0190-9622</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0190-9622</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Acad</term><term>Acad dermatol</term><term>American academy</term><term>Amyopathic</term><term>Amyopathic dermatomyositis</term><term>Arthritis</term><term>Arthritis rheum</term><term>Autoantibody</term><term>Azathioprine</term><term>Calcinosis</term><term>Calcinosis cutis</term><term>Callen</term><term>Clin</term><term>Connective tissue disease</term><term>Corticosteroid</term><term>Creatine</term><term>Curr</term><term>Cutaneous</term><term>Cutis</term><term>Cyclophosphamide</term><term>Dalakas</term><term>December</term><term>Dermatol</term><term>Dermatology</term><term>Dermatology december</term><term>Dermatology volume</term><term>Dermatomyositis</term><term>Engel</term><term>Engl</term><term>Erythematosus</term><term>Histopathologic</term><term>Hydroxychloroquine</term><term>Idiopathic</term><term>Immunoglobulin</term><term>Inflammatory</term><term>Inflammatory myopathies</term><term>Inflammatory myopathy</term><term>Intravenous</term><term>Juvenile dermatomyositis</term><term>Kovacs</term><term>Lancet</term><term>Lupus</term><term>Lymphocyte</term><term>Malignancy</term><term>Medsger</term><term>Methotrexate</term><term>Muscle weakness</term><term>Myalgia</term><term>Myopathy</term><term>Myositis</term><term>Neurol</term><term>Opin</term><term>Pachman</term><term>Pathol</term><term>Pediatr</term><term>Periorbital</term><term>Polymyositis</term><term>Rash</term><term>Rheum</term><term>Rheumatoid</term><term>Rheumatol</term><term>Scleroderma</term><term>Skin manifestations</term><term>Steroid</term><term>Syndrome</term><term>Synthetase</term><term>Systemic lupus erythematosus</term><term>Targoff</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Abstract: Dermatomyositis is a rare inflammatory myopathy with characteristic skin manifestations and muscular weakness. The disease can be categorized as adult idiopathic, juvenile, or amyopathic dermatomyositis as well as that associated with a connective tissue disease or a malignancy. Immunologic factors are most likely involved in the pathogenesis of the disease; however, genetic and environmental issues may also play important roles. Treatment with immunosuppressive agents has proved successful in the majority of patients, although significant morbidity still occurs. (J Am Acad Dermatol 1998;39:899-920.) Learning Objective: At the conclusion of this learning activity, participants should be familiar with the clinical characteristics of adult idiopathic, juvenile, and amyopathic dermatomyositis as well as the histopathologic and immunopathologic characteristics of the disease.</div></front></TEI><affiliations><list><country><li>États-Unis</li></country><region><li>État de New York</li></region></list><tree><country name="États-Unis"><region name="État de New York"><name sortKey="Kovacs, Stephen O" sort="Kovacs, Stephen O" uniqKey="Kovacs S" first="Stephen O." last="Kovacs">Stephen O. Kovacs</name></region><name sortKey="Kovacs, S Christine" sort="Kovacs, S Christine" uniqKey="Kovacs S" first="S. Christine" last="Kovacs">S. Christine Kovacs</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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