Acute promyelocytic leukemia

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(Redirected from Acute promyelocytic leukaemia)

Acute Promyelocytic Leukemia

Acute Promyelocytic Leukemia (APL) is a subtype of acute myeloid leukemia (AML), characterized by the accumulation of promyelocytes in the bone marrow. It is classified as AML-M3 in the French-American-British (FAB) classification system.

Pathophysiology[edit | edit source]

APL is caused by a specific chromosomal translocation, t(15;17)(q24;q21), which results in the fusion of the promyelocytic leukemia (PML) gene on chromosome 15 and the retinoic acid receptor alpha (RARA) gene on chromosome 17. This PML-RARA fusion protein interferes with normal hematopoiesis and leads to the accumulation of promyelocytes.

Clinical Presentation[edit | edit source]

Patients with APL often present with symptoms related to cytopenias and coagulopathy. Common symptoms include:

Diagnosis[edit | edit source]

The diagnosis of APL is confirmed through:

Treatment[edit | edit source]

The treatment of APL has been revolutionized by the introduction of all-trans retinoic acid (ATRA) and arsenic trioxide (ATO). The standard treatment regimen includes:

  • Induction therapy with ATRA and ATO
  • Consolidation therapy to eliminate residual disease
  • Maintenance therapy to prevent relapse

Prognosis[edit | edit source]

The prognosis for patients with APL has improved significantly with modern treatment protocols. The 5-year survival rate is over 80% with appropriate therapy. Early diagnosis and treatment are crucial to prevent complications such as DIC.

Complications[edit | edit source]

Complications of APL include:

See Also[edit | edit source]

External Links[edit | edit source]

  • [American Cancer Society: Acute Promyelocytic Leukemia]
  • [Leukemia & Lymphoma Society: APL]




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