Özet:

The trombophilic condition association between Evans syndrome and trombosis syndrome is quite rare. The incident-muz was diagnosed with ITP in March 2009 (trombocytes: 5710), 3 months after their follow-up on the development of deep venous thrombosis (DVT) and family history and acne risk factors were excluded after the mutation of heterozigot factor V leiden was identified. One year anticoagulant treatment was given with low molecular weight heparin (DMAH). After 7 months of diagnosis with the cause of the incident, splenectomy was performed as a second stage treatment. In the follow-up of the splenectomy-responsive phenomenon, the development of anemia was examined and Evans syndrome was diagnosed. After 16 months of Splenectomy, a long-term DMAH treatment was planned for the phenomenon that developed the second DVT attack. After 19 months of splenectomy, the hemogram was normal and lost with sudden death as a result of a possible thrombosis-related complication while there was no blood diet.