Serveur d'exploration Chloroquine

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Dermatomyositis

Identifieur interne : 003305 ( Main/Exploration ); précédent : 003304; suivant : 003306

Dermatomyositis

Auteurs : Jeffrey P. Callen [États-Unis]

Source :

RBID : ISTEX:BF35AF259703FDD803E649F8D545D8791B2FD161

English descriptors

Abstract

Abstract: Dermatomyositis and polymyositis are related disorders of unknown cause in which immunologic changes may be important. They sometimes overlap with other collagen vascular diseases, and not infrequently are associated with malignancy. The clinical features of the adult and juvenile forms of the disorder and the visceral manifestations of DM-PM are outlined, along with enzymatic, electromyographic, and histologic aids to diagnosis. While the cutaneous lesions often are resistant to treatment, systemic involvement may respond to corticosteroids or to immunosuppressive drugs. Treatment definitely alters the prognosis in cases not associated with malignancy.

Url:
DOI: 10.1016/0011-5029(87)90022-8


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

<record>
<TEI wicri:istexFullTextTei="biblStruct">
<teiHeader>
<fileDesc>
<titleStmt>
<title>Dermatomyositis</title>
<author>
<name sortKey="Callen, Jeffrey P" sort="Callen, Jeffrey P" uniqKey="Callen J" first="Jeffrey P." last="Callen">Jeffrey P. Callen</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:BF35AF259703FDD803E649F8D545D8791B2FD161</idno>
<date when="1987" year="1987">1987</date>
<idno type="doi">10.1016/0011-5029(87)90022-8</idno>
<idno type="url">https://api.istex.fr/ark:/67375/6H6-4BMKQMKJ-R/fulltext.pdf</idno>
<idno type="wicri:Area/Istex/Corpus">000D09</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">000D09</idno>
<idno type="wicri:Area/Istex/Curation">000D09</idno>
<idno type="wicri:Area/Istex/Checkpoint">002064</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">002064</idno>
<idno type="wicri:Area/Main/Merge">003377</idno>
<idno type="wicri:Area/Main/Curation">003305</idno>
<idno type="wicri:Area/Main/Exploration">003305</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title level="a">Dermatomyositis</title>
<author>
<name sortKey="Callen, Jeffrey P" sort="Callen, Jeffrey P" uniqKey="Callen J" first="Jeffrey P." last="Callen">Jeffrey P. Callen</name>
<affiliation wicri:level="2">
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Associate Professor of Dermatology University of Louisville School of Medicine Louisville, Kentucky</wicri:regionArea>
<placeName>
<region type="state">Kentucky</region>
</placeName>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series>
<title level="j">Disease-a-Month</title>
<title level="j" type="abbrev">YMDA</title>
<idno type="ISSN">0011-5029</idno>
<imprint>
<publisher>ELSEVIER</publisher>
<date type="published" when="1987">1987</date>
<biblScope unit="volume">33</biblScope>
<biblScope unit="issue">5</biblScope>
<biblScope unit="page" from="239">239</biblScope>
<biblScope unit="page" to="305">305</biblScope>
</imprint>
<idno type="ISSN">0011-5029</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">0011-5029</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="Teeft" xml:lang="en">
<term>Abnormality</term>
<term>Active disease</term>
<term>Arch dermatol</term>
<term>Arch intern</term>
<term>Arthralgia</term>
<term>Arthritis</term>
<term>Arthritis rheum</term>
<term>Autoantibody</term>
<term>Azathioprine</term>
<term>Behan</term>
<term>Benbassat</term>
<term>Biopsy</term>
<term>Bohan</term>
<term>Bony prominences</term>
<term>Calcification</term>
<term>Callen</term>
<term>Carcinoma</term>
<term>Cardiac</term>
<term>Cardiac disease</term>
<term>Case report</term>
<term>Childhood dermatomyositis</term>
<term>Childhood disease</term>
<term>Chronic graft</term>
<term>Clin</term>
<term>Clin rheum</term>
<term>Connective tissue disease</term>
<term>Corticosteroid</term>
<term>Corticosteroid therapy</term>
<term>Creatine</term>
<term>Creatine kinase</term>
<term>Cutaneous</term>
<term>Cutaneous disease</term>
<term>Cutaneous lesions</term>
<term>Cutaneous vasculitis</term>
<term>Cytotoxic</term>
<term>Dermatol</term>
<term>Dermatomyositis</term>
<term>Dysphagia</term>
<term>Electron microscopy</term>
<term>Engel</term>
<term>Engl</term>
<term>Enzyme levels</term>
<term>Erythematosus</term>
<term>Esophageal</term>
<term>Esophageal abnormalities</term>
<term>Esophageal disease</term>
<term>Esophageal dysmotility</term>
<term>Further studies</term>
<term>Greater risk</term>
<term>Heliotrope rash</term>
<term>Histopathologic</term>
<term>Host disease</term>
<term>Hydroxychloroquine sulfate</term>
<term>Immune</term>
<term>Immune complexes</term>
<term>Immunofluorescence</term>
<term>Immunoglobulin</term>
<term>Immunoglobulin deposition</term>
<term>Immunohistochemical studies</term>
<term>Immunologic</term>
<term>Immunosuppressive</term>
<term>Immunosuppressive agent</term>
<term>Immunosuppressive agents</term>
<term>Immunosuppressive drug</term>
<term>Immunosuppressive drugs</term>
<term>Immunosuppressive therapy</term>
<term>Inflammatory</term>
<term>Intern</term>
<term>Interstitial</term>
<term>Interstitial lung disease</term>
<term>Interstitial pneumonitis</term>
<term>Jdms</term>
<term>Juvenile dermatomyositis</term>
<term>Kinase</term>
<term>Lancet</term>
<term>Lesion</term>
<term>Lupus</term>
<term>Lupus erythematosus</term>
<term>Major criteria</term>
<term>Malignancy</term>
<term>Manchul</term>
<term>Metastatic disease</term>
<term>Methotrexate</term>
<term>Mononuclear cells</term>
<term>Multiple patients</term>
<term>Muscle biopsy</term>
<term>Muscle disease</term>
<term>Muscle fibers</term>
<term>Muscle tenderness</term>
<term>Muscle weakness</term>
<term>Muscular dystrophy</term>
<term>Myocarditis</term>
<term>Myopathy</term>
<term>Myositis</term>
<term>Myositis patient</term>
<term>Myositis patients</term>
<term>Neoplasm</term>
<term>Neural neurosurg psychiatry</term>
<term>Neurology</term>
<term>Oral corticosteroids</term>
<term>Other diseases</term>
<term>Other disorders</term>
<term>Ovarian cancer</term>
<term>Overlap</term>
<term>Overlap groups</term>
<term>Overlap myositis</term>
<term>Overlap patients</term>
<term>Overlap syndromes</term>
<term>Papanicolaou smear</term>
<term>Papule</term>
<term>Pathogenesis</term>
<term>Periungual</term>
<term>Periungual telangiectasias</term>
<term>Photosensitivity</term>
<term>Plasmapheresis</term>
<term>Polymyositis</term>
<term>Poor prognostic sign</term>
<term>Prednisone</term>
<term>Prednisone therapy</term>
<term>Pregnancy</term>
<term>Prognosis</term>
<term>Prognostic</term>
<term>Proximal</term>
<term>Proximal myopathy</term>
<term>Pulmonary disease</term>
<term>Pulmonary fibrosis</term>
<term>Pulse therapy</term>
<term>Rare patient</term>
<term>Rash</term>
<term>Remission</term>
<term>Rheum</term>
<term>Rheumatoid</term>
<term>Rheumatoid arthritis</term>
<term>Rheumatoid factor</term>
<term>Rheumatoid myositis</term>
<term>Rheumatol</term>
<term>Schwarz</term>
<term>Scleroderma</term>
<term>Semin</term>
<term>Semin arthritis rheum</term>
<term>Serologic</term>
<term>Serologic testing</term>
<term>Side effects</term>
<term>Skeletal muscle</term>
<term>Skin changes</term>
<term>Skin disease</term>
<term>Skin lesions</term>
<term>Steroid</term>
<term>Steroid therapy</term>
<term>Subsequent malignancies</term>
<term>Symmetrical muscle weakness</term>
<term>Syndrome</term>
<term>Systemic lupus erythematosus</term>
<term>Telangiectasias</term>
<term>Therapy</term>
<term>Tissue diseases</term>
<term>Tissue disorders</term>
<term>Total body irradiation</term>
<term>Tymms</term>
<term>Unpublished data</term>
<term>Urinary sediment</term>
<term>Vasculitis</term>
<term>Vasculopathic</term>
<term>Vasculopathic process</term>
<term>Viral</term>
<term>Winkelmann</term>
<term>Younger patients</term>
</keywords>
</textClass>
<langUsage>
<language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Abstract: Dermatomyositis and polymyositis are related disorders of unknown cause in which immunologic changes may be important. They sometimes overlap with other collagen vascular diseases, and not infrequently are associated with malignancy. The clinical features of the adult and juvenile forms of the disorder and the visceral manifestations of DM-PM are outlined, along with enzymatic, electromyographic, and histologic aids to diagnosis. While the cutaneous lesions often are resistant to treatment, systemic involvement may respond to corticosteroids or to immunosuppressive drugs. Treatment definitely alters the prognosis in cases not associated with malignancy.</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>États-Unis</li>
</country>
<region>
<li>Kentucky</li>
</region>
</list>
<tree>
<country name="États-Unis">
<region name="Kentucky">
<name sortKey="Callen, Jeffrey P" sort="Callen, Jeffrey P" uniqKey="Callen J" first="Jeffrey P." last="Callen">Jeffrey P. Callen</name>
</region>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Sante/explor/ChloroquineV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 003305 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 003305 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    ChloroquineV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     ISTEX:BF35AF259703FDD803E649F8D545D8791B2FD161
   |texte=   Dermatomyositis
}}

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Wed Mar 25 22:43:59 2020. Site generation: Sun Jan 31 12:44:45 2021