What are the FAB classifications of acute myeloid leukemia?
The FAB classification of acute myeloid leukemia (AML) generally includes M1 (acute myeloblastic leukemia, minimally differentiated), M2 (acute myeloblastic leukemia with maturation), M3 (acute promyelocytic leukemia), M4 (acute myelomonocytic leukemia), and M5 (acute monocytic leukemia). A detailed analysis is as follows:

1. M1 (Acute Myeloblastic Leukemia, Minimally Differentiated): Characterized by a very high proportion of myeloblasts in the bone marrow with low differentiation. Patients commonly present with anemia, bleeding, and infections. Peripheral white blood cell counts are often elevated. Treatment primarily involves chemotherapy, and prognosis is influenced by the patient's age and overall health status.
2. M2 (Acute Myeloblastic Leukemia with Maturation): Features a high proportion of myeloblasts in the bone marrow along with some promyelocytes and more mature cells. Clinical manifestations are similar to those of M1; some patients may develop hepatosplenomegaly. Treatment strategies should be tailored based on cytogenetic characteristics.
3. M3 (Acute Promyelocytic Leukemia): Dominated by promyelocytes in the bone marrow, which contain numerous abnormal granules. Patients are prone to severe bleeding complications. However, this subtype shows excellent response to retinoic acid therapy, and with proper treatment, the prognosis is relatively favorable.
4. M4 (Acute Myelomonocytic Leukemia): Involves abnormal proliferation of both granulocytic and monocytic lineages in the bone marrow. In addition to common symptoms, patients may experience skin infiltration or gingival swelling. Treatment must target malignant clones from both cell lineages.
5. M5 (Acute Monocytic Leukemia): Characterized by predominant involvement of monoblasts and immature monocytes in the bone marrow. Patients are prone to extramedullary infiltration, such as gingival hyperplasia and skin nodules. Peripheral blood monocyte counts are significantly elevated. Intensive chemotherapy is required to control disease progression.
Accurate FAB classification relies on morphological examination of bone marrow cells. After diagnosis, individualized treatment plans should be developed incorporating immunophenotyping and genetic features. Regular follow-up bone marrow examinations and complete blood counts are essential for monitoring therapeutic response. Patients should take precautions against infection and bleeding and maintain balanced nutrition to tolerate treatment effectively.