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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
1992-12-17
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pubmed:abstractText |
Idiopathic thrombocytopenic purpura (ITP) is a disease characterized by the presence of circulating antiplatelet antibodies, which can cause platelet destruction, through the mediation of the reticuloendothelial system (RES). We report on a patient affected with ITP insensible to first line steroid therapy, who achieved a complete response following the administration of high-dose immunoglobulins (HDIgG, 400 mg/kg/die for 5 days), in association with decreasing doses of steroids. At the end of the treatment with immunoglobulins, the patient presented a normal platelet count and, up to date, 5 moths from the end of therapy, he is in good shape and presents normal platelets values.
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pubmed:language |
ita
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0026-4806
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
83
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
571-4
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:1436610-Adolescent,
pubmed-meshheading:1436610-Bone Marrow,
pubmed-meshheading:1436610-Humans,
pubmed-meshheading:1436610-Immunoglobulins, Intravenous,
pubmed-meshheading:1436610-Male,
pubmed-meshheading:1436610-Platelet Count,
pubmed-meshheading:1436610-Prednisone,
pubmed-meshheading:1436610-Purpura, Thrombocytopenic, Idiopathic,
pubmed-meshheading:1436610-Remission Induction
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pubmed:year |
1992
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pubmed:articleTitle |
[The infusion of high-dose immunoglobulins in a case of idiopathic thrombocytopenic purpura].
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pubmed:affiliation |
Divisione di Medicina, Ospedale Civile, Tortona, Alessandria.
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pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|