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245 Possible Causes for Prolymphocytic Leukemia

  • Chronic Lymphocytic Leukemia

    The diseases included: chronic lymphocytic leukemia (CLL), 400; prolymphocytic leukemia, 22; hairy cell leukemia (HCL), 40; HCL variant, 15; splenic lymphoma with villous[] Two years after the onset of B-CLL, CLL cells acquired CD38 antigen expression and the disease entity became CLL/prolymphocytic leukemia.[] (CLL / prolymphocytic leukemia): 10 - 55% prolymphocytes Prolymphocytic leukemia: 55% prolymphocytes Clinical features Most common adult leukemia in Western countries, less[]

  • B-Cell Prolymphocytic Leukemia

    B-cell Prolymphocytic Leukemia[] B-cell prolymphocytic leukemia is a relatively rare lymphoproliferative disorder. No specific cytogenetic abnormality has yet been associated with it.[] Abstract We describe clonal chromosome abnormalities in 13 new cases of B-cell type prolymphocytic leukemia (B-PLL) investigated using pokeweed, lipopolysaccharide B, TPA[]

  • Prolymphocytic Leukemia

    Described as a type of leukemia having a rather poor prognosis, prolymphocytic leukemia (PLL) is a rare lymphoid malignancy of mature T or B cells.[] Prolymphocytic leukemia is divided into two types according to the kind of cell involved: B-cell prolymphocytic leukemia and T-cell prolymphocytic leukemia.[] Leukemia, Prolymphocytic, B-Cell/therapy* Leukemia, Prolymphocytic, T-Cell/diagnosis* Leukemia, Prolymphocytic, T-Cell/genetics Leukemia, Prolymphocytic, T-Cell/therapy Transplantation[]

  • Hairy Cell Leukemia Variant

    HCL and prolymphocytic leukemia.[] Hairy-cell leukemia variant (HCl-V) is a district clinico-pathological entity with intermediate features between classical HCl (HCl-C) and B-cell prolymphocytic leukemia.[] HCL-V is thought to represent a hybrid between prolymphocytic leukemia and HCL, the nucleus more closely resembling a prolymphocyte and the cytoplasm a hairy cell.[]

  • T-Cell Prolymphocytic Leukemia

    Other names include T-cell chronic lymphocytic leukemia, "knobby" type of T-cell leukemia, and T-prolymphocytic leukemia/T-cell lymphocytic leukemia.[] The three cases of ocular prolymphocytic leukemia, including the one case of ocular T-cell prolymphocytic leukemia, are discussed in detail as well as 14 reported clinical[] Abstract A diagnosis of prolymphocytic leukemia was made from the blood and bone marrow of a 50 year old man.[]

  • Leukemia

    T-cell prolymphocytic leukemia (T-PLL) can involve extramedullary sites, but the diagnosis is usually established by examination of blood and bone marrow.[] Jeffrey Medeiros, T-Cell Prolymphocytic Leukemia Involving Extramedullary Sites, American Journal of Clinical Pathology, Volume 123, Issue 3, March 2005, Pages 456–464, Download[] T-cell prolymphocytic leukemia (T-PLL) is the most common type of mature T-cell leukemia and is characterized by a rapidly rising peripheral blood lymphocyte count, bone marrow[]

  • Hairy Cell Leukemia

    You are here Home Types of Cancer Leukemia - B-cell Prolymphocytic Leukemia and Hairy Cell Leukemia Leukemia - B-cell Prolymphocytic Leukemia and Hairy Cell Leukemia This[] Hairy cell leukemia (HCL) variant is a rare low-grade B-cell disorder affecting the elderly or middle-aged population with features intermediate between those of HCL and prolymphocytic[] Cancer.Net Guide Leukemia - B-cell Prolymphocytic Leukemia and Hairy Cell Leukemia[]

  • Anemia

    BACKGROUND: Posterior reversible encephalopathy syndrome is a neurotoxic condition that occurs as a result of the failure of posterior circulatory autoregulation in response to acute changes in blood pressure. Overperfusion with resultant disruption of the blood-brain barrier results in vasogenic edema, but not[…][]

  • Rosacea

    This report describes a patient with a rosacea-like eruption as a unique clinical presentation of T-cell prolymphocytic leukemia.[] Depending on the type of leukemia, a wide range of clinical and histopathological findings may be encountered.[]

  • Thrombocytopenia

    Abstract The association of immune thrombocytopenic with malaria is a rare event. We describ the case of a young soldier who, after returning from Central Africa, presented a fever associated with petechial purpura and gingivorrhagia, hemogram showed deep thrombocytopenia and macrocytic normochrome anemia, thick[…][]

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