Evans syndrome is a rare syndrome associated with the presence of autoimmune hemolytic anemia and simultaneous or sequential development of thrombocytopenia. It was first described by Evan and Duane in Evans Syndrome A rare autoimmune disorder that is a combination of two or more immune hematological disorders in which the immune system destroys the body's red blood cells, white blood cells and/or platelets.
May 18, · Evans syndrome is a very rare autoimmune disorder in which the immune system destroys the body's red blood cells, white blood cells and/or platelets. Affected people often experience thrombocytopenia (too few platelets) and Coombs' positive hemolytic anemia (premature destruction of red blood cells). Feb 04, · Evans syndrome is a rare disorder that causes the immune system to destroy certain blood cells. It can cause low blood cell levels and anemia, which may lead to a variety of symptoms. Treatments.
Oct 08, · Evans syndrome (ES) is a rare disease characterized by the simultaneous or sequential development of autoimmune hemolytic anemia (AIHA) and immune thrombocytopenia (ITP) and/or immune neutropenia. To better describe the characteristics and outcome of ES in adults, a survey was initiated in Cited by: