Autoimmune hepatitis (AIH), which predominantly affects women and usually responds to immunosuppressive therapy, is a disease characterized by hypergammaglobulinemia, increased titers of serum tissue autoantibody, and an immunogenetic background. This disease can present with a variety of coexisting non-hepatic disorders presumably caused by immune dysregulation. Here we present a male AIH patient with coexisting Idiopathic thrombocytopenic Purpura (ITP) and Autoimmune Hemolytic Anemia (AIHA) which is rarely reported.