Source:http://linkedlifedata.com/resource/pubmed/id/18057462
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
2007-12-6
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pubmed:abstractText |
We describe three patients with progressive fibrosing interstitial lung disease (ILD) as the first and only manifestation of systemic sclerosis. In one patient the presence of anti-Scl-70 autoantibodies suggested systemic sclerosis to be the underlying cause of the disease. In the two other subjects, however, anti-Scl-70 antibodies were negative. In these patients the lung disease preceded other manifestations of systemic sclerosis by several years. Diagnosis, prognosis and treatment of systemic sclerosisassociated ILD is discussed.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0300-2977
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
65
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
390-4
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pubmed:meshHeading |
pubmed-meshheading:18057462-Adult,
pubmed-meshheading:18057462-Female,
pubmed-meshheading:18057462-Humans,
pubmed-meshheading:18057462-Lung Diseases, Interstitial,
pubmed-meshheading:18057462-Male,
pubmed-meshheading:18057462-Middle Aged,
pubmed-meshheading:18057462-Prognosis,
pubmed-meshheading:18057462-Scleroderma, Systemic
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pubmed:year |
2007
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pubmed:articleTitle |
Interstitial lung disease as the first manifestation of systemic sclerosis.
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pubmed:affiliation |
Department of Pulmonology, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands.
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pubmed:publicationType |
Journal Article,
Case Reports
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