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Case Study: Acute Myeloid Leukemia (AML)

Jun 20, 2024

Case Study: Acute Myeloid Leukemia (AML)

Patient Presentation

  • Patient: 45-year-old man
  • Symptoms: Fever (acute onset), fatigue, bone pain, gum bleeding
  • Examinations:
    • External: gum bleeding, thermal tenderness
    • Laboratory findings:
      • Hemoglobin: Low (indicative of anemia)
      • WBC count: High (possible infection)
      • Platelet count: Very low (50,000)
  • Peripheral Blood Smear: Presence of Auer rods

Diagnosis

  • Condition: Acute Myeloid Leukemia (AML)
    • Presence of Auer rods in myeloblasts confirms AML.
    • Differential diagnosis excludes chronic myeloid leukemia (CML) as CML lacks Auer rods.

Classification of AML

  • WHO Classification:
    • Acute myeloid leukemia with genetic abnormalities (e.g., translocations 8;21, inv(16), t(15;17))
    • AML with myelodysplasia-related changes
    • Therapy-related AML
    • AML not otherwise classified (Refer to FAB classification)
  • FAB Classification:
    • M0: Minimally differentiated
    • M1: Without maturation
    • M2: With maturation
    • M4: Myelomonocytic
    • M5: Monoblastic/Monocytic (M5a and M5b)
    • M6: Erythroid
    • M7: Megakaryoblastic
    • Notably, M1, M2, M4, M6 are Myeloperoxidase positive.

Specific Cytochemical Stains

  • Myeloperoxidase (MPO): Positive in immature myeloid cells containing granules and Auer rods. Negative in M0 myeloblast.
  • Sudan Black B: Positive in immature cells in AML.
  • Periodic Acid-Schiff (PAS): Positive in immature lymphoid cells and erythroid leukemia cells.
  • Non-Specific Esterase: Positive in monocytic series (M4 and M5).
  • Acid Phosphatase: Shows focal positivity in leukemic blasts and diffuse reaction in monocytic cells; also positive in Acute Lymphoblastic Leukemia (ALL).

Important Points

  • Fever and acute onset symptoms lead towards a differential diagnosis involving infections and leukemia.
  • Peripheral smears with Auer rods make a strong case for AML diagnosis.
  • High WBC count with anemia and low platelets are critical laboratory findings supporting AML.
  • WHO and FAB classifications provide a detailed subclassification of different AML types based on genetic and morphological criteria.
  • Understanding cytochemical stains is crucial for the differential diagnosis and confirmation of AML subtypes.