• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

How to study your flashcards.

Right/Left arrow keys: Navigate between flashcards.right arrow keyleft arrow key

Up/Down arrow keys: Flip the card between the front and back.down keyup key

H key: Show hint (3rd side).h key

A key: Read text to speech.a key

image

Play button

image

Play button

image

Progress

1/19

Click to flip

19 Cards in this Set

  • Front
  • Back
What is the hallmark of a chronic leukemia?
Proliferation of a neoplastic clone that exhibits partial maturation into recognizable myeloid cells or lymphocytes.
What are the two most common chronic leukemias?
1) Chronic Myelogenous Leukemia
2) Chronic Lymphocytic Leukemia
Of what cluster of diseases is CML a member?
The Myeloproliferative Disorders (P Vera, Essential Thrombocythemia, Primary Myelofibrosis)
What are the common features of the Myeloproliferative Disorders?
1) Origin in a pluripotent stem cell
2) Clonal nature of disease
3) Normal maturation of cells in early stages of disease
4) Elevation of one or more blood counts
5) Capacity to transform into CML
What is the susceptible population for CML?
Age >40, equal between sexes. Approx. 20% of adult leukemia is CML
What are the presenting symptoms of CML?
Often asymptomatic. Fatigue, weight loss, fevers and sweats are possible.
What is the hallmark of CML?
Leukocytosis is the hallmark of CML, with blood counts from 25K to 300K
What are predominant cell types in CML?
Mature PMNs and Bands, with excess eosinophils, basophils and platelets also common.
What do peripheral blast cells indicate in CML?
Blast cells in CML indicate an advancing disease, eventually appearing like acute leukemia with >20% blasts
How does the marrow present in CML?
Hypercellular with GRANULOCYTE precursors and mild fibrosis
Name the disease.
Chronic Myelogenous Leukemia
What tissues are commonly involved in CML?
Splenomegaly is common in CML, and may cause an increase in girth or early satiety.
What is the characteristic molecular abnormality in CML?
A Philadelphia translocation, t(9:22), forming the bcr-abl oncogene.
What are some of the complications with classifying CML?
1) Differentiation from P Veray or ET
2) Sometimes confused with a normal, physiologic Leukemoid Reaction following infection
What is a Leukemoid Reaction?
A physiologic leukocytosis in response to stress or infection.
What test may be used to differentiate CML from a Leukemoid Reaction?
Leukocyte Alkaline Phosphatase Test
* LAP score is INCREASED in Leukemoid
* LAP score is VERY LOW in CML
What are the three phases of CML progression?
1) Stabe/Chronic Phase - commonly asymptomatic
2) Accelerated Phase - beginnings of left shift. Symptomatic.
3) Blast Crisis - similar to acute leukemia. Terminal stage.
What new drug works wonders with CML in the chronic phase?
Imatinib, a monclonal antibody inhibitor of the ABL Tyrosine Kinase enzyme.
How are CML blast crisis patients treated?
Typically with transplant.