Leukemia Flashcards

1
Q

Leukemia

A

malignant transformation of WBCs. Myeloid or lymphoid

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2
Q

acute leukemia versus chronic leukemia

A

acute- immature

chronic- mature

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3
Q

acute lymphoblastic/ lymphocytic leukemia

A

rapid proliferation of immature lymphocytes

occurs primarily in children
young children, ages 2-5
whites

MC cancer in children
Down syndrome (we ALL fall Down)
H and P
bone pain
frequent infections
anemia (fatigue, dyspnea on exertion, pallor, thrombocytopenia)
lymphadenopathy
hepatosplenomegaly

PBS: abundant blasts

PAS and TdT positive

Philadelphia chromosome t[9;22], found in 15% of adult ALL cases

Treatment: Imatinib, targets Philadelphia chromosome tumors

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4
Q

chronic myelogenous leukemia

A

proliferation of mature granuloctytes

midlife, can be associated with radiation exposure

feared complication: blast crisis
mature myeloid cells transform into immature blasts, thus blast crisis can be fatal

H and P:
possibly asymptomatic
fatigue
weightloss, nightsweats, hepatosplenomegaly

Labs:
no smudge cells
very high WBC
increasd myeloid precursors (promyelocytes, myelocytes, and metamyelocytes)

Philadelphia chromosome
almost always CML
(t[9;22] BCR-ABL, which is an oncogene tyrosine kinase always switched on)

Treatment:
imatinib

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5
Q

Acute myelogenous leukemia

A

Proliferation of immature myeloid cells

20% are blast

fatigue, easy bruising, frequent infections, unlike ALL you DO NOT see a lot of bone pain

Bone marrow biopsy shows blasts (myeloid cell line)
Myeloperoxidase positive

PBS:
Auer rods in the cytoplasm of blasts
notched nuclei

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6
Q

Chronic lymphocytic leukemia

A

mature B cells
elderly patients

H and P: similar to Hodgkin lymphoma
fatigue
frequent infections
night sweats
fevers
lymphadenopathy
hepatosplenomegaly
may be asymptomatic
Labs:
increased WBC (>100,000)

Bone marrow biopsy:
mature lymphs filling up the marrow space

slides:
Smudge cells (lymphocytes tear apart when you put them on a glass slide)
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7
Q

Hairy cell leukemia

A

looks hairy
better prognosis than CML

fatigue
frequent infections
abdominal fullness
massive splenomegaly
no lymphadenopathy
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8
Q

Myelodysplastic syndrome

A

ineffective production of WBCs
pre-leukemic state (could progress to cancer)

keep a close eye on these

typically, hypogranulated PMNs and
hyperlobular granulocytes with nuclei

Anemia (macrocytosis)
Polycythemia vera is a type

The pseudo-Pelger-Huet anomaly:
PMNs have nuclei with 2 lobes connected by a thin strand

Treatment: 
monitor for progression
Transfusions
Growth factors
Stem cell transplant
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9
Q

Oncology therapy

A

Surgery
Radiation
Chemotherapy

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10
Q

Most common neoplasm in children

A

ALL

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11
Q

most common leukemia in adults

A

CLL

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12
Q

Philadelphia chromosome is almost always seen

A

CML

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13
Q

Smudge cells on peripheral smear

A

CLL

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14
Q

Peripheral blasts are PAS+ and TdT+

A

ALL

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15
Q

Peripheral blasts are PAS-, myeloperoxidase +, and have Auer rods

A

AML

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16
Q

Pancytopenia in a Down syndrome patient

A

ALL

17
Q

Associated with translocation 9;22

A

ALL, CML, AML

primarily CML

18
Q

WBCs with hair-like projections

A

hairy cell leukemia

19
Q

medication as/w 95% remission in CML

A

Imatinib