Acute promyelocytic leukemia

Acute promyelocytic leukemia (APML, APL) is a subtype of acute myeloid leukemia (AML), a cancer of the white blood cells. In APL, there is an abnormal accumulation of immature granulocytes called promyelocytes. The disease is characterized by a chromosomal translocation involving the retinoic acid receptor alpha (RARA) gene and is distinguished from other forms of AML by its responsiveness to all-trans retinoic acid (ATRA; also known as tretinoin) therapy. Acute promyelocytic leukemia was first characterized in 1957 by French and Norwegian physicians as a hyperacute fatal illness, with a median survival time of less than a week. Today, prognoses have drastically improved; 10-year survival rates are estimated to be approximately 80-90% according to one study.

Acute promyelocytic leukemia
Bone marrow smear from a patient with acute promyelocytic leukemia, showing characteristic abnormal promyelocytes.
SpecialtyHematology and oncology
Usual onset~40 years old
CausesUncontrolled proliferation of promyelocytes
FrequencyDevelops in about 600 to 800 people per year (United States)
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