医学
免疫学
血小板减少性紫癜
细小病毒
抗体
免疫系统
背景(考古学)
风疹
并发症
疾病
病毒
接种疫苗
内科学
麻疹
生物
古生物学
作者
Dita Smíšková,Zuzana Blechová,Libuše Polanecká,Jitka Zítová,Marie Podojilová,Petr Smíšek
出处
期刊:PubMed
日期:2013-03-01
卷期号:19 (1): 15-8
被引量:2
摘要
Immune thrombocytopenia (immune thrombocytopenic purpura, ITP) is an acquired autoimmune disease, mediated by antibodies against platelet glycoproteins. ITP can develop in the context of other disorders (secondary ITP), including acute and chronic infections (HIV, H. pylori, HCV, HBV, CMV, EBV, VZV, parvovirus B19, rubella, etc.). The case reports present two children and one adult with ITP complicating VZV, EBV and HAV infections. Corticosteroids are usually initial drugs, but they are controversial in case of ITP during acute infections. Intravenous immunoglobulins are preferred, especially in children, because of their smaller suppression of inflammatory response. Two of the patients were successfully treated with intravenous immunoglobulins. In the remaining patient, corticosteroid therapy had good but delayed effects as compared to immunoglobulins.
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