Literature DB >> 23945832

[Immune thrombocytopenia as a complication of acute infectious diseases - case reports].

Dita Smíšková1, Zuzana Blechová, Libuše Polanecká, Jitka Zítová, Marie Podojilová, Petr Smíšek.   

Abstract

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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Year:  2013        PMID: 23945832

Source DB:  PubMed          Journal:  Klin Mikrobiol Infekc Lek        ISSN: 1211-264X


  1 in total

1.  Severe thrombocytopenia and recurrent epistaxis associated with primary Epstein-Barr virus infection.

Authors:  William Tilden; Shahnawaz Valliani
Journal:  BMJ Case Rep       Date:  2015-04-09
  1 in total

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