Lenka Lisá, Ivana Plameňová, Ján Sýkora, Kamil Zeleňák, Juraj Sokol, Peter Kubisz
Thrombosis is quite rare in childhood and adolescence and usually is associated with hereditary thrombophilia, hereditary vascular anomaly – e.g. May-Thurner syndrome and important acquired provoking factors. Combination of these factors may lead to enlarged or recurrent iliofemoral thrombosis in young adults or adolescents. Authors describe here a case of 18-years old patient with thrombosis due to May-Thurner syndrome and multiple hereditary thrombophilia.