Author/Editor		Glaser, Marjana; Glaser, Andrej; Skalicky, Marjan
Title		Primarna imunska trobocitopenija odraslih
Translated title		Primary adult immune thrombocytopenia
Type		članek
Source		In: Krajnc I, Pahor A, Skok P, et al, editors. Zbornik predavanj in praktikum 22. srečanje internistov in zdravnikov družinske medicine Iz prakse za prakso; 2011 maj 20-21; Maribor. Maribor: Univerzitetni klinični center,
Publication year		2011
Volume		str. 69-80
Language		slo
Abstract		Immune adult thrombocytopenia (idiopathic thrombocytopenic purpura) (ITP) comprises a group of disorders, characterized by isolated, autoimmune mediated thrombocytopenia and thrombopoiesis impairment. ITP may occur in the absence of an preliminary cause as primary or it is the result of other diseases, secondary. The diagnosis of ITP is of exclusion. Clinical signs of the disease are diverse, bleeding into the skin, mucosa, from viscera or into central nervous system occur, when the platelet number is less then 20 x 10 on 9/L. In the paper, the authors are presenting the recommendations for the diagnosis of ITP the recent treatment options for adults and pregnant women.
Summary		Imunska trombocitopenija odraslih (idiopatska trombocitopenična purpura (ITP) je skupek bolezni, katerih značilnost je pojav izolirane, avtoimunsko vodene trombocitopenije in motene trombopoeze. ITP se lahko pojavi brez predhodnega vzroka kot primarna ali je posledica drugih bolezni, sekundarna. Diagnoza ITP je izključitvena. Klinični znaki so raznoliki, krvavitve v kožo, sluznice, iz notranjih organov ali v centralni živčni sistem pa se parviloma pojavljajo pri številu trombocitov pod 20 x 10 na 9/L. Poleg trenutno priporočenih postopkov za ugotavljanje ITP, so predstavljene najnovejše smernice zdravljenja ITP odraslih in nosečnic.
Descriptors		THROMBOCYTOPENIA PURPURA, THROMBOCYTOPENIC, IDIOPATHIC