Hematologic Malignancies 1 Flashcards
When should you suspect hematologic malignancy?
- Bone marrow is not functioning normally and can’t find an explanation –> low cell counts, high cell counts, or bone marrow cells in the blood
- Lymphatic tissues have enlarged and infectious etiology can’t be found
What is a blast?
Leukocyte that has 3 or 4 of these features:
- Large cell
- High nuclear to cytoplasmic ratio
- Prominent, single or multiple nucleoli
- Immature (faint) chromatin
- Appearance is shared by many cells on a slide
What are Auer rods?
Needle like eosinophilic crystals formed by proteins normally found in secondary granules –> typically myeloperoxidase
–> Always diagnostic of myeloid blasts
What happens to bone marrow cellularity as you age?
Cellularity decreases –> Approximation is 100- age = % cellularity
Limitations of flow cytometry in cell counting
- RBC lysis procedure destroys erythroid precursors as well
- Unusually large cells won’t be counted correctly
- Cells can’t be immediately correlated with detailed morphological features
Ways flow cytometry counts cells
- Forward scatter detects cell size
2. Side scatter is high for cells with granules or segmented nuclei
Flow cytometry and immunophenotyping
Fluorescent antibodies against CD45 (all bone marrow cells), CD34 (hematopoietic stem cells), or CD33 (granulocytes) plotted against side scatter to cluster cell types
Philadelphia chromosome
9;22 translocation –> routine cytogenetic finding in chronic myelogenous leukemia
Key advantage of FISH genotyping
Cells do not have to be growing to detect chromosomal abnormalities
3 types of hematologic malignancies
- Acute leukemia –> rapidly proliferating clones
- Myeloproliferative disease –> Chronically proliferating and differentiating clones
- Myelodysplastic syndrome –> poorly functioning clones
Cells involved in to acute myeloid leukemia
- Myeloid lineage
- Erythroid lineage
- Megakaryocytes
Cells involved in acute undifferentiated leukemia
Hematopoietic stem cells
Mutations in AML that blocks differentiation
PML-RARA (transcription factor), Tet1, Tet2 (inactivation of methylation), IDH1 and 2 (
Mutations in AML that enhance proliferation
DNMT3A (DNA methylation enzyme), FLT3, KIT –> mostly tyrosine kinases with constitutive activity
Mutation causing genetic instability in AML
TP53 mutation in both alleles –> leads to translocations, deletions, and fragmentation