How is Acute Myeloid Leukemia Diagnosed?

Published: May 23, 2024

Diagnosing Acute Myeloid Leukemia (AML) involves a series of tests and evaluations. Here's what you need to know.

Blood Tests

The first step in diagnosing AML is usually a complete blood count (CBC) to check for abnormal levels of white blood cells, red blood cells, and platelets. If the CBC indicates possible leukemia, a blood smear is examined under a microscope to look for leukemia cells.

Bone Marrow Examination

A bone marrow biopsy and aspiration are typically performed to confirm AML. During this procedure, a small amount of bone marrow is removed and examined for leukemia cells. This test provides detailed information about the types and numbers of cells in the marrow.

Acute Myeloid Leukemia (AML) is diagnosed through blood tests and bone marrow examinations. These diagnostic procedures are crucial for determining the presence and extent of leukemia.

Genetic Testing

Genetic tests are conducted to identify specific mutations or chromosomal changes in leukemia cells. These tests help classify the type of AML, guide treatment decisions, and predict patient outcomes.

Frequently Asked Questions

A CBC is a blood test that measures various blood cell levels.

A biopsy confirms the presence of leukemia cells in the marrow.

They identify mutations that guide treatment and prognosis.

Key Takeaways

Accurate diagnosis is crucial for effective treatment planning and management.

Curious about the diagnosis process? Chat with Doctronic to learn more.

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References

Arber DA, Orazi A, Hasserjian RP, et al. International Consensus Classification of Myeloid Neoplasms and Acute Leukemias: integrating morphologic, clinical, and genomic data. Blood 2022; 140:1200.

Duncavage EJ, Bagg A, Hasserjian RP, et al. Genomic profiling for clinical decision making in myeloid neoplasms and acute leukemia. Blood 2022; 140:2228.

Always discuss health information with your healthcare provider.