Source:http://linkedlifedata.com/resource/pubmed/id/16957888
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2007-1-9
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pubmed:abstractText |
Acquired amegakaryocytic thrombocytopenia (AAT) is a rare disorder, characterized by severe thrombocytopenia and selective, marked decrease or absence of megakaryocytes in the bone marrow. We describe a 29-year-old female with adult onset Still's disease preceding a diagnosis of AAT and autoimmune hemolytic anemia, which was successfully treated with cyclosporine. This is the first case of AAT in a patient with adult onset Still's disease.
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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 |
0172-8172
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
27
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
295-8
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pubmed:meshHeading |
pubmed-meshheading:16957888-Adult,
pubmed-meshheading:16957888-Anemia, Hemolytic, Autoimmune,
pubmed-meshheading:16957888-Antirheumatic Agents,
pubmed-meshheading:16957888-Cyclosporine,
pubmed-meshheading:16957888-Female,
pubmed-meshheading:16957888-Humans,
pubmed-meshheading:16957888-Megakaryocytes,
pubmed-meshheading:16957888-Platelet Transfusion,
pubmed-meshheading:16957888-Still's Disease, Adult-Onset,
pubmed-meshheading:16957888-Thrombocytopenia
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pubmed:year |
2007
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pubmed:articleTitle |
Successful treatment of acquired amegakaryocytic thrombocytopenia with cyclosporine in adult onset Still's disease.
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pubmed:affiliation |
Division of Rheumatology, The Hospital for Rheumatic Diseases, Hanyang University, Seoul, 133-792, South Korea.
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pubmed:publicationType |
Journal Article,
Case Reports
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