Leukemias Flashcards

(41 cards)

1
Q

myelodysplastic syndrome

A

chronic cytopenia (anemia, neutropenia, thrombocytopenia)
abnormal cell maturation
hematologic condition
pre-leukemia
may do bone marrow biopsy
risk for anemia, infection, bleeding/bruising, AML

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2
Q

leukemia

A

hematologic malignancy
cancer of bone marrow
affect the blood and lymph tissue
symptoms include fatigue, infections, bleeding, bruising
treated via chemo and bone marrow transplant
leukemic cells crowd bone marrow
decreased function and production of normal cells in bone marrow
leukemic infiltrates (pain, swelling in joints, organomegaly)

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3
Q

acute leukemia

A

abnormal proliferation of immature blood cells for 1-5 months
cells nonfunctional
affects lymphoblasts and myeloblasts

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4
Q

chronic leukemia

A

abnormal proliferation of immature blood cells for 2-5 yrs
decreased function of cells
affects mature lymphocytes and immature myeloid cells

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5
Q

risk factors for leukemia

A

down syndrome
radiation
benzene
viruses
drugs (alkylating agents)-> 1/4 happen after chemo

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6
Q

acute leukemia symps

A

fatigue
abdominal fullness
infection
bleeding
pancytopenia
lymphadenopathy
hepatosplenomegaly
CNS involvement
leukostasis

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7
Q

leukostasis

A

systemic hyperleukocytosis
medical emergency
seen in AML
elevated blast count w/ symps respiratory and/or neurological distress
treated via leukapheresis and cytoreduction

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8
Q

acute leukemia diagnosis

A

bone marrow biopsy
peripheral blood smear
cytogenetics (crucial for prognosis and treatment)

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9
Q

acute leukemia imaging and procedures

A

chest xray
MUGA scan
lumbar puncture
venous access placement
leukpheresis

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10
Q

types of acute leukemia

A

AML
APL
ALL

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11
Q

complications of acute leukemia

A

transfusions (graft vs host and alloimmunization)
infection (neutropenic fever)
tumor lysis syndrome (rapid tumor breakdown after chemo)

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12
Q

treatment of acute leukemia

A

chemo
stem cell implant
supportive care
highest risk of relapse (first 3 yrs)-> so followup!

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13
Q

AML

A

median age 67 yrs old
exposure to ionizing radiation and benzene
chemo
meds
progresses quickly

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14
Q

symptoms of AML

A

fever and infection
bleeding, mucosal, cutaneous (petechiae and bruising)
fatigue and dyspnea (anemia)

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15
Q

AML labs

A

normocytic
normochromic
thrombocytopenia
>20% myeloblasts
auer rod diagnostics
confirmation of diagnosis via myeloid specific surface markers
remission= return of normal peripheral count and <5% blasts in bone marrow

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16
Q

treatments of AML

A

remission induction chemo
intensive
post-remission therapy
stem cell transplant

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17
Q

ALL

A

most common type of leukemia in children (ages 2-5)
affect precursor B-cells
pre B can develop into burkitt’s lymphoma
starry skey appearance of tumor of cytogenic analysis
affect precursor T cell in adolescents

18
Q

ALL assessment

A

pallor
fever
bone pain
splenomegaly
ecchymosis
lymphadenopathy

19
Q

ALL labs

A

leukopenia
thrombocytopenia
anemia
lymphoblasts (>20%)
bone marrow biopsy (>20% blasts)
cell analysis shows B and T cell linage, NK lineage

20
Q

ALL treatment

A

LP prior to treatment
chemo (3 phases)-> induction therapy, CNS prophylaxis, post-remission therapy (high dose)
bone marrow transplant

21
Q

ALL prognosis

A

children and adults less than 39 years of age= 90% remission and cure-rate 60-80%
older adults= remission rate 80% and cure rate 20-40%

22
Q

ALL good prognosis

A

<30 yrs
WBC= <50k

23
Q

ALL poor prognostic factors

A

elevated blasts
delayed remission
blasts in CSF

24
Q

chronic leukemia

A

long median survival, but not curable
CML and CLL

25
CML
median age 55-65 risk factors include ionizing radiation philly chromosome (translocation of chromosome 9 and 22)
26
symptoms of CML
splenomegaly (1st symp) early satiety fever in blast crisis
27
CML labs
WBC=>100k anemia (normocystic, normochromic) thrombocytosis
28
CML assessment
bone marrow biopsy cytogenetic analysis
29
CML treatment
TKIs HCTs pallitative care w/ chemo
30
CLL
most common adult (71 yrs old)leukemia orange agent highest familial risk of all hematology malignancies
31
CLL symps
asymp splenomegaly hepatomegaly lymphadenopathy (painless)
32
CLL labs
leukocytosis lymphocytosis anemia thrombocytopenia smudge cells
33
3 disease phases of CML
chronic phase accelerated phase blast crisis
34
chronic phase
< 5% blasts palpable splenomegaly
35
accelerated phase
6-30% blasts increased number of precursors and blasts
36
blast crisis
30-40% bone marrow is blasts leukocytic lesions= form as a result of high cell number-> thrombosis low survival rate (3 months)
37
what does AML affect?
myeloblasts
38
what does CML affect?
granulocytes neutrophils mature and immature myeloid cells
39
what does CLL affect?
lymphocytes
40
what does ALL affect?
lymphoblasts
41
APL
subtype of AML (most common adult leukemia) treated with vit. A along w/ chemo A-rod (auer rods) plays for the NY Yankee's in the big APL