Sézary Syndrome is a rare leukemic cutaneous T-cell lymphoma with unknown etiology and an aggressive clinical course. It is characterized by erythroderma, generalized lymphadenopathy and neoplastic CD4+ memory T cells called Sézary cells in the skin, lymph nodes and peripheral blood. The early course of the disease is usually misdiagnosed because skin lesions may be atypical for several years because … Preberite več >>