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Treatment of a patient with classical paroxysmal nocturnal hemoglobinuria and Budd-Chiari syndrome, with complement inhibitor eculizumab: Case Report

Background. Paroxysmal nocturnal haemoglobinuria (PNH) is a rare acquired clonal disorder of hematopoietic stem cells involving all blood cells. Erythrocytes have increased susceptibility to complement-mediated haemolysis. Thrombosis is the leading cause of mortality and follows episodes of acute he...

תיאור מלא

שמור ב:
מידע ביבליוגרפי
Main Authors: Mandala, E, Lafaras, C, Goulis, I, Tsioni, K, Georgopoulou, V, Ilonidis, G
פורמט: Artigo
שפה:Inglês
יצא לאור: SOCIETY OF "FRIENDS OF HIPPOKRATIA JOURNAL" 2013
נושאים:
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC3738287/
https://ncbi.nlm.nih.gov/pubmed/23935352
תגים: הוספת תג
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