問題一覧
1
M0 origin
myelocytic
2
AML, minimally differentiated
M0
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MPO: NEGATIVE SBB: NEGATIVE
M0
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M0 MPO: SBB:
negative
5
M0 AML, ___ DIFFERENTIATED
minimally
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M1 ORIGIN
myelocytic
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AML, WITHOUT MATURATION
M1
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M1 AML
without maturation may demonstrate auer rods
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most common subtype of AML may demonstrate auer rods
M2
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AML WITH MATURATION
M2
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origin of M2
myelocytic
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m3 origin
myelocytic
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M3
ACUTE PROMYELOCYTIC LEUKEMIA (APL)
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associated with DIC- DISSEMINATED INTRAVASCULAR COAGULATION FAGGOT CELLS
M3
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M3 associated with
DIC- DISSEMINATED INTRAVASCULAR COAGULATION FAGGOT CELLS
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microgranular variant cells have the characteristics "butterfly" "bowtie" "coin-on-coin" "apple core"
M3V,APL
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M3V, APL microgranular variant cells have the characteristics
"butterfly" "bowtie" "coin-on-coin" "apple core"
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bundles of auer rods
faggot cell
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m4 origin
myelocytic monocytic
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M4 IS ? AKA
ACUTE MYELOMONOCYTIC LEUKEMIA (AMML) NAEGELI MONOCYTIC LEUKEMIA
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2nd most common subtype of AML may demonstrate auer rods
m4
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AMML, w/ increased marrow eosinophils
M4E
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m5 origin
monocytic
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M5 IS AKA?
ACUTE MONOCYTIC LEUKEMIA (AMoL) schilling leukemia
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AMoL, well differentiated seen in middle aged adults <80% monoblast in BM
M5b
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M5b AMoL, ? seen in ? ?monoblast in BM
well differentiated middle aged adults <80%
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AMoL, poorly differentiated
M5a
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M5a, AMoL ? seen in? ? monoblast in Bm
poorly differentiated children >80%
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M6 origin
Erythrocytic Myelocytic
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M6 ? AKA?
Acute Erythroleukemia Digugliemos Syndrome
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M6 type of anemia
macrocytic, normochromic
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Acute Erythroleukemia Aka Digugliemos Syndrome may demonstrate Auer rods
M6
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erythroid cells in AML M6:
PAS=Strongly (+)
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origin of M7
Megakaryocytic
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M7 AKA
ACUTE MEGAKARYOCYTIC LEUKEMIA
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requires immunocytochem. staining for accurate diagnosis
M7
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m7 requires immunocytochem. staining for accurate diagnosis (?)
Factor VIII STAIN +
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AML M8
ACUTE BASOPHILIC LEUKEMIA
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ACUTE BASOPHILIC LEUKEMIA
AML M8
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myelocytic (+) in
MPO, SBB, SE
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+ MPO, SBB, SE
myelocytic
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monocytic + in
nse ( butyrate) nse (acetate)
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+ nse butyrate nse acetate
MONOCYTIC