Dermatomyositis
Identifieur interne : 002468 ( Main/Exploration ); précédent : 002467; suivant : 002469Dermatomyositis
Auteurs : Jeffrey P. Callen [États-Unis]Source :
- The Lancet [ 0140-6736 ] ; 2000.
English descriptors
- Teeft :
- Acad, Acad dermatol, Amyopathic dermatomyositis, Bony prominences, Calcinosis, Callen, Corticosteroid, Curr opin rheumatol, Cutaneous, Cutaneous disease, Cutaneous lesions, Cutaneous manifestations, Dermatol, Dermatomyositis, Dysphagia, Erythematosus, Heliotrope, Heliotrope rash, Immunosuppressive, Immunosuppressive drugs, Intravenous immunoglobulin, Juvenile dermatomyositis, Lesion, Lupus, Lupus erythematosus, Malignant, Malignant disease, Muscle disease, Muscle involvement, Muscle weakness, Myopathy, Myositis, Papule, Polymyositis, Poor prognosis, Pulmonary involvement, Rash, Rheumatol, Skin lesions, Systemic corticosteroids, Telangiectasia.
Abstract
Summary: Dermatomyositis is one of the idiopathic inflammatory myopathies with characteristic cutaneous manifestations including the heliotrope rash, Gottron's papules, cuticular changes including periungual telangiectasia, a photodistributed erythema or poikiloderma, and a scaly alopecia. Dermatomyositis has been linked to cancer, particularly ovarian cancer. Cancer-associated disease is more commonly found in older patients, and when present, is associated with a poor prognosis. A childhood form of the disease exists and is frequently complicated by the development of calcinosis. Dermatomyositis is a systemic disorder and whereas the skin and muscles are the most commonly affected organs, patients may have arthralgias, arthritis, oesophageal disease, or cardiopulmonary dysfunction. Recently described serological abnormalities, known as myositis-specific antibodies, add credence to the notion that this disorder is distinct from all other collagen-vascular diseases, and may lead to important discoveries about the pathogenesis of the inflammatory myopathies, which are not currently of practical use in the clinic or office. Management of the patient with myositis usually includes systemic corticosteroids with or without an immunosuppressive agent. Cutaneous disease is more difficult to manage, but antimalarials, methotrexate, and intravenous immunoglobulin are effective in small, often open-label, studies.
Url:
DOI: 10.1016/S0140-6736(99)05157-0
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 000326
- to stream Istex, to step Curation: 000326
- to stream Istex, to step Checkpoint: 001285
- to stream Main, to step Merge: 002496
- to stream Main, to step Curation: 002468
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:392B5A44A5FF000AC1B1A368C7CD6770BADD5634</idno>
<date when="2000" year="2000">2000</date>
<idno type="doi">10.1016/S0140-6736(99)05157-0</idno>
<idno type="url">https://api.istex.fr/ark:/67375/6H6-1XDX9D8D-5/fulltext.pdf</idno>
<idno type="wicri:Area/Istex/Corpus">000326</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">000326</idno>
<idno type="wicri:Area/Istex/Curation">000326</idno>
<idno type="wicri:Area/Istex/Checkpoint">001285</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">001285</idno>
<idno type="wicri:Area/Main/Merge">002496</idno>
<idno type="wicri:Area/Main/Curation">002468</idno>
<idno type="wicri:Area/Main/Exploration">002468</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>Division of Dermatology, University of Louisville, 310 East Broadway, Suite 200, Louisville, KY 40202</wicri:regionArea>
<placeName><region type="state">Kentucky</region>
</placeName>
</affiliation>
<affiliation></affiliation>
<affiliation></affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j">The Lancet</title>
<title level="j" type="abbrev">LANCET</title>
<idno type="ISSN">0140-6736</idno>
<imprint><publisher>ELSEVIER</publisher>
<date type="published" when="2000">2000</date>
<biblScope unit="volume">355</biblScope>
<biblScope unit="issue">9197</biblScope>
<biblScope unit="page" from="53">53</biblScope>
<biblScope unit="page" to="57">57</biblScope>
</imprint>
<idno type="ISSN">0140-6736</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0140-6736</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Acad</term>
<term>Acad dermatol</term>
<term>Amyopathic dermatomyositis</term>
<term>Bony prominences</term>
<term>Calcinosis</term>
<term>Callen</term>
<term>Corticosteroid</term>
<term>Curr opin rheumatol</term>
<term>Cutaneous</term>
<term>Cutaneous disease</term>
<term>Cutaneous lesions</term>
<term>Cutaneous manifestations</term>
<term>Dermatol</term>
<term>Dermatomyositis</term>
<term>Dysphagia</term>
<term>Erythematosus</term>
<term>Heliotrope</term>
<term>Heliotrope rash</term>
<term>Immunosuppressive</term>
<term>Immunosuppressive drugs</term>
<term>Intravenous immunoglobulin</term>
<term>Juvenile dermatomyositis</term>
<term>Lesion</term>
<term>Lupus</term>
<term>Lupus erythematosus</term>
<term>Malignant</term>
<term>Malignant disease</term>
<term>Muscle disease</term>
<term>Muscle involvement</term>
<term>Muscle weakness</term>
<term>Myopathy</term>
<term>Myositis</term>
<term>Papule</term>
<term>Polymyositis</term>
<term>Poor prognosis</term>
<term>Pulmonary involvement</term>
<term>Rash</term>
<term>Rheumatol</term>
<term>Skin lesions</term>
<term>Systemic corticosteroids</term>
<term>Telangiectasia</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front><div type="abstract">Summary: Dermatomyositis is one of the idiopathic inflammatory myopathies with characteristic cutaneous manifestations including the heliotrope rash, Gottron's papules, cuticular changes including periungual telangiectasia, a photodistributed erythema or poikiloderma, and a scaly alopecia. Dermatomyositis has been linked to cancer, particularly ovarian cancer. Cancer-associated disease is more commonly found in older patients, and when present, is associated with a poor prognosis. A childhood form of the disease exists and is frequently complicated by the development of calcinosis. Dermatomyositis is a systemic disorder and whereas the skin and muscles are the most commonly affected organs, patients may have arthralgias, arthritis, oesophageal disease, or cardiopulmonary dysfunction. Recently described serological abnormalities, known as myositis-specific antibodies, add credence to the notion that this disorder is distinct from all other collagen-vascular diseases, and may lead to important discoveries about the pathogenesis of the inflammatory myopathies, which are not currently of practical use in the clinic or office. Management of the patient with myositis usually includes systemic corticosteroids with or without an immunosuppressive agent. Cutaneous disease is more difficult to manage, but antimalarials, methotrexate, and intravenous immunoglobulin are effective in small, often open-label, studies.</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 002468 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 002468 | 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:392B5A44A5FF000AC1B1A368C7CD6770BADD5634 |texte= Dermatomyositis }}
This area was generated with Dilib version V0.6.33. |