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Chronic Myeloid Leukemia

 

 

Diagnosis

CML is often identified through routine blood tests for other medical reasons. 

Complete medical history and physical examination are the first investigations.

Hyperleukocytosis with granulocytes in peripheral blood and bone marrow supports CML diagnosis. 

BCR-ABL rearrangement establishes diagnosis.

 

Peripheral Blood Film:

 

The peripheral blood from a patient with CML shows:

  • Borderline anemia with normocytic and normochromic cells.
  • Occasional elliptocytes are present (not shown in the image provided).
  • Metamyelocytes are present with myelocytes and promyelocytes present also. Blast cells may also be found.
  • The neutrophils have a normal morphology and show prominent granulation.
  • The basophils appear slightly hypogranulated and are increased along with eosinophils and monocytes.
  • There is an increased number of platelets with occasional platelet clumping and large forms present (not shown in image provided).

 

 

Diagnostic Procedures for CML:

Signs of Disease

Physical examination

  • Generally unwell
  • Enlarged spleen
  • Pallor
  • Low-grade fever
  • Echymoses
  • Sternal tenderness

 

Complete blood count

  • Excessive immature white blood cells

 

Blood tests

  • Increased vitamin B-12 binding proteins
  • Decreased levels of leukocyte alkaline phosphatase

 

Cytogenetic analysis

  • Presence of Philadelphia chromosome

 

Bone marrow aspiration and biopsy

  • Presence of abnormal cells
  • Hypercellular
  • Spectrum of mature and immature granulocytes
  • Increased eosinophils and basophils
  • Increased megakaryocytes

 


 

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