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University revision · Hematology

Acute Myeloid Leukaemia

This comprehensive topic addresses Acute Myeloid Leukaemia (AML), the most common acute leukaemia in adults. It is a cornerstone of advanced haematology education for Zambian university and diploma students. The material defines AML based on the accumulation of myeloid blast cells (>20% in marrow) and explains its pathogenesis through acquired mutations in genes regulating proliferation, differentiation, and apoptosis (e.g., FLT3, NPM1, DNMT3A). Both the FAB morphological and the contemporary WHO classification systems are covered, with the latter emphasising genetic abnormalities. The clinical presentation, dominated by sequelae of bone marrow failure (severe infections, anaemia, bleeding) and occasional tissue infiltration (e.g., gums, skin), is detailed. The diagnostic laboratory evaluation is a major focus, including peripheral blood smear examination for blasts and Auer rods, bone marrow assessment, and the pivotal role of cytochemistry (Myeloperoxidase, Sudan Black B) and immunophenotyping (CD13+, CD33+) in confirming myeloid lineage. For tertiary learners, mastery of AML requires understanding the link between genetic subtypes, clinical behaviour, and prognosis. This knowledge is essential for interpreting lab reports, contributing to treatment discussions, and succeeding in professional examinations for careers in haematology, oncology, or medical laboratory science in Zambia.

Questions
100
Est. time
~100 min
Views
0
Pass mark
50%

How this revision works

Outcomes

If you passOutstanding! You have mastered the complexities of AML, including its genetic landscape, classification systems, and detailed diagnostic methodology. Your ability to correlate morphology, cytochemistry, and immunophenotyping is a critical skill for any future haematopathology practitioner.
If you don't pass yetAML diagnosis relies on a systematic approach. Ensure you are comfortable with the definition (>20% blasts) and the key cytochemical stains (MPO, SBB) that confirm myeloid lineage. Review the common genetic mutations and how they fit into the WHO classification. A structured review will clarify these concepts.

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