ALL Flashcards

1
Q
  1. Contrast acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL) in regards to demographics of affected patients, and prognosis.
A
AML = Affects adults mostly
ALL = Affects children mostly with good cure rate.  Rarer in adults where prognosis is worse
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2
Q

Explain the concept of a “leukemic stem cell”.

A

in patients with acute leukemia there is a population of self-renewing cells that, in essence, provides an inexhaustible source of the leukemic cells that replace the bone marrow.

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3
Q
  1. List risk factors for acute leukemia, while recalling that the majority of acute leukemias occur in the apparent absence of risk factors.
A
  • Previous chemotherapy, especially DNA alkylating agents and topoisomerase-II inhibitors
  • Marrow exposure to ionizing radiation

Others…

  • Tobacco smoke
  • Benzene exposure
  • Genetic syndromes including Down syndrome, Bloom syndrome, Fanconi anemia, and ataxia-telangiectasia.
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4
Q

List common signs and symptoms exhibited by patients with acute leukemia at initial presentation, and explain the reasons for these findings.

A

Present because of normal marrow replacement, so:
- Anemia: fatigue, malaise, pallor, dyspnea
- Thrombocytopenia: bruising, petechiae, hemorrhange
- Neutropenia: fever, infections
OR
Directly attributable to leukemic cells
- High WBC count = Inc viscosity = Thrombotic event
- DIC: clotting & clot-lysis = strokes, bleeding
- Direct infiltration of tissues (skin, gums)

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5
Q

List methods for immunophenotyping in acute leukemias, and list a few basic markers that would help to assign blasts to a precursor-B, precursor-T, or myeloid lineage.

A
Take biopsy and add Ab (IHC) or flow 
CD34 = immaturity
TdT = Common LYMPHOBLAST
Bcell = CD19 CD22 (lack Ig & CD20, mature)
Tcell = CD3 CD7
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6
Q

Contrast B-ALL and T-ALL in regards to patient age and sex, manner of manifestation, and prognosis.

A

In contrast to B-ALL, T-ALL…

  • adolescents & young adults
  • Component of T-LBL (mediastinal mass)
  • Markedly elevated WBC
  • Favors males
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7
Q

List 3 commonly observed cytogenetic abnormalities in B-ALL, and recall the usual patient age group and prognosis associated with these abnormalities.

A

9;22 BCR-ABL: “Philly” / Adults / WORST prognosis
MLL (11q23): neonates & infants; poor prog
t(12;21); childhood; very good prog

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8
Q

List 5 factors affecting prognosis in ALL.

A

Worst prognosis for…

  • Age: worst for 10, adults
  • WBC count: markedly elevated at Dx
  • Slow response to therapy / small amounts of residual disease after therapy
  • # of chromosomes: hyper (50-66) is good, hypo (<46) is bad
  • B vs. T: T-ALL is worse
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