Leukemia Flashcards

1
Q

Polycythemia dx

A

BM Bx: hypercellular & absent Fe stores

Splenomegaly

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2
Q

Essential Thrombocythemia Dx

A

Platelet count >450,000

BM Bx: megakaryocytes in clusters

MUST RULE OUT FE DEFICIENCY

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3
Q

CML Dx

A

philadelphia chromosome

Increased WBC: 100-200K

BCR/ABL gene

<5% blasts

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4
Q

polycythemia tx

A

phlebotomy

low dose ASA

high risk pts:

Hydroxyurea

Intereferon

Busulfan

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5
Q

Essential Thrombocythemia tx

A

low dose ASA

int-high risk:

hydroxyurea

INC RISK FOR thrombosis and hemorrhage

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6
Q

CML tx

A

allogenic SCT

dz control:

  • tyrosine kinase inhibitors: inibs
  • palliative: hydroxyurea, intereferon +/-cytarabine
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7
Q

AML dx

A

auer rod

pancytopenia w/circulating blasts

leukocytosis >200K

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8
Q

AML tx

A

chemo: 3+7 protocol

anthracycline + cytarabine

TOC: allogenic SCT

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9
Q

CLL dx

A

increased WBC with lymphocytosis

SMUDGE cells

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10
Q

CLL tx

A

bendamustine & rituximab

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11
Q

do you have enlarged spleen or LAD in aplastic anemia?

A

NO

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12
Q

PE of hairy cell leukemia

A

palpable splenomegaly

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13
Q

dx hairy cell leukemia

A

CBC: pancytopenia w/low monocytes

BM Bx: Hairy cells

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14
Q

CPx of PV

A

pruiritis after warm bath/shower

tinnitus

early satiety

erythromelalgia of hands and feet

facial plethora

excoriated skin

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15
Q

Mutation involved in both PV and essential thrombocythemia

A

JAK 2

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16
Q

overproduction of myeloid cells

A

CML

17
Q

Which disorder can you have a blast cell crisis in?

A

CML

18
Q

sx of blast crisis

A

fatigue

night sweats

low grade fever

pain from splenomegaly

19
Q

biggest diff b/w AML and ALL

A

age:

AML: 60s

ALL: 3-7 y/old

20
Q

AML sx

A

CNS manifestations

easy bruising/bleeding

frequent infections

fever

21
Q

What is the MC lymphoid leukemia

A

CLL

22
Q

aplastic anemia tx

A

allogenic SCT

or

immunosuppresion

23
Q
A