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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1992-5-28
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pubmed:abstractText |
A patient with CREST syndrome (calcinosis cutis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia) who had severe jaundice (total bilirubin 29.1 mg/dl) and rapidly progressive liver damage is reported. The liver damage findings matched the criteria of autoimmune chronic active hepatitis (CAH). There have been no prior reports of a case of CREST syndrome with autoimmune CAH in Japan. Anticentromere antibody (ACA) was detected in the serum; ACA seemed to be related to the pathogenesis of these two diseases.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0918-2918
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
31
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
69-73
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:1568046-Autoantibodies,
pubmed-meshheading:1568046-Autoimmune Diseases,
pubmed-meshheading:1568046-Calcinosis,
pubmed-meshheading:1568046-Centromere,
pubmed-meshheading:1568046-Esophageal Motility Disorders,
pubmed-meshheading:1568046-Female,
pubmed-meshheading:1568046-Hepatitis, Chronic,
pubmed-meshheading:1568046-Humans,
pubmed-meshheading:1568046-Liver Diseases,
pubmed-meshheading:1568046-Middle Aged,
pubmed-meshheading:1568046-Raynaud Disease,
pubmed-meshheading:1568046-Syndrome,
pubmed-meshheading:1568046-Telangiectasis
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pubmed:year |
1992
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pubmed:articleTitle |
A case of CREST syndrome with rapidly progressive liver damage.
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pubmed:affiliation |
Department of Medicine, Aoto Hospital, Jikei University School of Medicine, Tokyo, Japan.
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pubmed:publicationType |
Journal Article,
Case Reports
|