Acute Myeloid Leukemia (AML): Key Symptoms, Causes, Diagnosis, and Treatment Insights
Michael Schopis
Michael Schopis 13 years ago
Board-Certified Gastroenterologist & Hepatologist #Sexual Wellness
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Acute Myeloid Leukemia (AML): Key Symptoms, Causes, Diagnosis, and Treatment Insights

Explore comprehensive insights into Acute Myeloid Leukemia (AML), a blood and bone marrow cancer primarily affecting adults. Learn about its symptoms, causes, risk factors, classification, diagnosis methods, treatment options, prognosis, and prevention strategies.

Understanding Acute Myeloid Leukemia (AML)

Acute Myeloid Leukemia (AML) is a fast-growing cancer that originates in the blood and bone marrow, primarily impacting the body's white blood cells (WBCs). This condition leads to the production of abnormal, immature white blood cells that multiply rapidly, disrupting normal blood cell function.

AML is also referred to by several other names including acute myelocytic leukemia, acute myelogenous leukemia, acute granulocytic leukemia, and acute non-lymphocytic leukemia.

Annually, approximately 19,520 new AML cases are diagnosed in the United States, according to the National Cancer Institute (NCI).

Recognizing AML Symptoms

Early AML symptoms may mimic common flu signs such as fever and fatigue. Additional symptoms include:

  • Persistent bone pain
  • Frequent nosebleeds
  • Bleeding or swollen gums
  • Easy bruising
  • Excessive night sweating
  • Shortness of breath
  • Unexplained weight loss
  • Heavier menstrual periods in females

Causes and Risk Factors of AML

AML arises due to genetic mutations in the DNA regulating bone marrow cell development. These mutations cause the bone marrow to produce numerous immature white blood cells known as myeloblasts, which accumulate and replace healthy cells, impairing immune function.

While the exact cause of these DNA mutations is unclear, exposure to certain chemicals, radiation, and chemotherapy drugs may contribute.

Risk factors increasing AML likelihood include:

  • Advanced age (median diagnosis age is 68 years)
  • Male gender
  • Cigarette smoking
  • Exposure to chemicals like benzene
  • Pre-existing blood disorders such as myelodysplastic syndromes (MDS)
  • Genetic conditions like Down syndrome

However, having risk factors does not guarantee AML development, and AML can occur without any known risk factors.

Classification of AML

The World Health Organization (WHO) categorizes AML into several groups based on genetic and clinical features, including:

  • AML with recurrent genetic abnormalities
  • AML with myelodysplasia-related changes
  • Therapy-related myeloid neoplasms
  • AML not otherwise specified
  • Myeloid sarcoma
  • Myeloid proliferations associated with Down syndrome
  • Acute leukemia of ambiguous lineage

Subtypes within these groups often reflect specific chromosomal or genetic mutations, such as AML with t(8;21) involving a chromosomal translocation between chromosomes 8 and 21. Unlike many cancers, AML is not staged traditionally.

Diagnosing AML

Diagnosis begins with a physical examination checking for liver, lymph node, and spleen enlargement, alongside blood tests to assess anemia and white blood cell counts.

Definitive diagnosis requires a bone marrow biopsy, where a sample is extracted from the hip or breastbone using a needle and analyzed in a lab. A lumbar puncture may also be performed to detect leukemia cells in spinal fluid.

Treatment Approaches for AML

AML treatment is divided into two main phases:

Remission Induction Therapy

This phase employs chemotherapy to eliminate leukemia cells rapidly. Hospitalization is common due to side effects like infection risk and bleeding from the destruction of healthy cells.

For acute promyelocytic leukemia (APL), targeted therapies such as arsenic trioxide or all-trans retinoic acid are used to inhibit leukemia cell growth.

Consolidation Therapy

Also known as post-remission therapy, consolidation aims to eradicate any remaining leukemia cells to prevent relapse. Stem cell transplantation may be necessary, using either donor cells or the patient's own previously stored stem cells.

Donor stem cell transplants carry higher risks but lower relapse chances, whereas autologous transplants have fewer risks but a higher possibility of relapse.

Long-Term Outlook and Survival Rates

Approximately two-thirds of AML patients achieve remission, with rates nearing 90% in APL cases. Five-year survival rates stand at about 27.4% for adults and 60-70% for children.

Early detection and prompt treatment significantly improve remission chances. A remission lasting over five years is generally considered a cure.

If AML symptoms appear, immediate consultation with a healthcare provider is critical, especially if infection signs or persistent fever occur.

Preventive Measures

To reduce AML risk, limit exposure to hazardous chemicals and radiation by using protective equipment. Regular medical check-ups for concerning symptoms are essential for early detection.

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