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CHRONIC MYELOGENOUS
LEUKEMIA(CML)
DR. SOMA THAKUR
M.D.(PATHOLOGY)
Definition
• A myeloproliferative neoplasm arising from abnormal pleuripotent
stem cell & associated with BCR-ABL fusion gene located in
Philadelphia chromosome,leading to uncontrolled proliferation of
granulocytes.
Epidemiology
• Incidnce -1-2 cases/100,000 population.
• Any age,more common- 50-60 yrs.
• Male>female
• Etiology-unknown,radiation exposure etc.
• Clinical feature -
Insiduous onset
Asymptomatic
Symptoms-fatigue,wt. loss,night sweats
hepatosplenomegaly,lymphadenopathy & anaemia.
1.CHRONIC PHASE
• Lasts for 3-4 years
• General examination-splenomegaly
• Cbc- leucocytosis with predominance of segmented neutrophils &
myelocytes,thrombocytosis usually.
• Pbs-2% blasts,basophilia,eosinophilia,monocytosis<3%
• Bone marrow- hypercellular with marked granulocytic proliferation with
significantly increased myelocytes
increased M:E ratio
megakaryocytes-variable.
Small ,hypolobate called as dwarf megakaryocyte is characteristic.
Bone marrow biopsy- increase in thickness of immature granulocyte along
bone trabeculae.
ACCELERATED PHASE
• Any one of following criteria:-
1.persistent/increasing wbc
2.persistent thrombocytosis unctrolled by therapy
3.persistent thrombocytopenia unrelated to therapy
4. clonal cytogenetic evolution occurring after initial diagnostic
karyotype
5.20% or more basophils in peripheral blood
6. 10-19% myeloblasts in blood or bone marrow.
BLAST PHASE
• Blasts>=20% of pb wbc or nucleated cells of bone marrow
or
• Extramedullary blasts proliferations(skin,ln,spleen,bone,cns etc.)
Diagnosis
• Philadelphia chromosome or BCR-ABL
• If no Philadelphia chromosome – FISH –to detect cryptic
transformation of BCR-ABL .
Differential diagnosis
• Infections
• Drugs
• Other myeloproliferative neoplasms like CNL & PV
THANK
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Chronic myelogenous leukemia(cml)

  • 2. Definition • A myeloproliferative neoplasm arising from abnormal pleuripotent stem cell & associated with BCR-ABL fusion gene located in Philadelphia chromosome,leading to uncontrolled proliferation of granulocytes.
  • 3. Epidemiology • Incidnce -1-2 cases/100,000 population. • Any age,more common- 50-60 yrs. • Male>female • Etiology-unknown,radiation exposure etc. • Clinical feature - Insiduous onset Asymptomatic Symptoms-fatigue,wt. loss,night sweats hepatosplenomegaly,lymphadenopathy & anaemia.
  • 4. 1.CHRONIC PHASE • Lasts for 3-4 years • General examination-splenomegaly • Cbc- leucocytosis with predominance of segmented neutrophils & myelocytes,thrombocytosis usually. • Pbs-2% blasts,basophilia,eosinophilia,monocytosis<3% • Bone marrow- hypercellular with marked granulocytic proliferation with significantly increased myelocytes increased M:E ratio megakaryocytes-variable. Small ,hypolobate called as dwarf megakaryocyte is characteristic. Bone marrow biopsy- increase in thickness of immature granulocyte along bone trabeculae.
  • 5. ACCELERATED PHASE • Any one of following criteria:- 1.persistent/increasing wbc 2.persistent thrombocytosis unctrolled by therapy 3.persistent thrombocytopenia unrelated to therapy 4. clonal cytogenetic evolution occurring after initial diagnostic karyotype 5.20% or more basophils in peripheral blood 6. 10-19% myeloblasts in blood or bone marrow.
  • 6. BLAST PHASE • Blasts>=20% of pb wbc or nucleated cells of bone marrow or • Extramedullary blasts proliferations(skin,ln,spleen,bone,cns etc.)
  • 7. Diagnosis • Philadelphia chromosome or BCR-ABL • If no Philadelphia chromosome – FISH –to detect cryptic transformation of BCR-ABL .
  • 8. Differential diagnosis • Infections • Drugs • Other myeloproliferative neoplasms like CNL & PV