A multicenter experience of thrombotic microangiopathies in Turkey: The Turkish Hematology Research and Education Group (ThREG)-TMA01 study
TRANSFUSION AND APHERESIS SCIENCE, cilt.57, sa.1, ss.27-30, 2018 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 57 Sayı: 1
- Basım Tarihi: 2018
- Doi Numarası: 10.1016/j.transci.2018.02.012
- Dergi Adı: TRANSFUSION AND APHERESIS SCIENCE
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Sayfa Sayıları: ss.27-30
- Anahtar Kelimeler: Thrombotic microangiopathy, Thrombotic thrombocytopenic purpura, Hemolytic-uremic syndrome, TTP, HUS
- Atatürk Üniversitesi Adresli: Evet
Özet
Thrombotic microangiopathies (TMAs) are rare, but life-threatening disorders characterized by microangiopathic hemolytic anemia and thrombocytopenia (MAHAT) associated with multiorgan dysfunction as a result of microvascular thrombosis and tissue ischemia. The differentiation of the etiology is of utmost importance as the pathophysiological basis will dictate the choice of appropriate treatment.