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  2. T-cell acute lymphoblastic leukemia - Wikipedia

    en.wikipedia.org/wiki/T-cell_acute_lymphoblastic...

    In childhood, T-cell acute lymphoblastic leukemia (T-ALL) patients can expect a 5-year event-free survival (EFS) rate of 70% and an overall survival (OS) rate of 80%. [1] Among the approximately 25% of children who relapse, survival rates drop to 30-50%, with patients generally showing a much poorer prognosis. [ 1 ]

  3. Acute lymphoblastic leukemia - Wikipedia

    en.wikipedia.org/wiki/Acute_lymphoblastic_leukemia

    Acute lymphoblastic leukemia (ALL) is a cancer of the lymphoid line of blood cells characterized by the development of large numbers of immature lymphocytes. [1] Symptoms may include feeling tired, pale skin color, fever, easy bleeding or bruising, enlarged lymph nodes, or bone pain. [1]

  4. Leukemia - Wikipedia

    en.wikipedia.org/wiki/Leukemia

    Specialty: Hematology and oncology: Symptoms: Bleeding, bruising, fatigue, fever, increased risk of infections [2] Usual onset: All ages, [3] most common in 60s and 70s. [4] It is the most common malignant cancer in children, but the cure rates are also higher for them.

  5. Acute leukemia - Wikipedia

    en.wikipedia.org/wiki/Acute_leukemia

    Acute leukemia or acute leukaemia is a family of serious medical conditions relating to an original diagnosis of leukemia. In most cases, these can be classified according to the lineage, myeloid or lymphoid , of the malignant cells that grow uncontrolled, but some are mixed and for those such an assignment is not possible.

  6. Biphenotypic acute leukaemia - Wikipedia

    en.wikipedia.org/wiki/Biphenotypic_acute_leukaemia

    Biphenotypic acute leukaemia (BAL) is an uncommon type of leukemia which arises in multipotent progenitor cells which have the ability to differentiate into both myeloid and lymphoid lineages. [1] [2] [3] It is a subtype of "leukemia of ambiguous lineage". [4] The direct reasons leading to BAL are still not clear.

  7. Mixed-phenotype acute leukemia - Wikipedia

    en.wikipedia.org/wiki/Mixed-phenotype_acute_leukemia

    It is a rare disease, constituting about 2–5% of all leukemia cases. [1] It mostly involve myeloid with either of T lymphocyte or B lymphocyte progenitors, but in rare cases all the three cell lineages. [2] Knowledge on the cause, clinical features and cellular mechanism is poor, making the treatment and management (prognosis) difficult. [3]

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