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71 Cards in this Set

  • Front
  • Back
7 T-cell asocciated CD molecules
CD1-5
CD7
CD8
CD45 is present on ___ but not on ___
nearly all hematolymphoid cells
HLy cells
CD10 aka ___ is present on ___
CALLA
immature B cells
CD20 is present on ___ but not ___
all mature B cells
plasma cells
CD23 is ___ and is present on ___ (2)
IgE R
activated mature germinal center B cells
follicular dendritic cells
CD79a is ___ and is present on ___
mIg
pre-B through plasma cells (?)
CD138 is ___ and is present on ___
adhesion molecule
late stage B cell differentiation including plasma cell
CD5 is expressed by most ___ and some ___
T cells
B cells
CD15 and CD30 are present on ___
Reed-Sternberg cells
CD34 is present on
HSCs
2 most common lys
DLBCLy
FLy
ALL and LBLy can be caused by ___ (2) cells
pre-B
pre-T
when caused by pre-B cells, ALL/LBLy will be positive for ___ (4)
CD10
CD19
CD79a
TdT
when caused by pre-T cells, ALL/LBLy will be positive for ___ (4)
CD2
CD5
CD7
TdT
80% of LBLy is from ___ cells.
80% of ALL is from ___ cells.
T
B
ALL is mostly in ___ (age).
LBLy is mostly in ___.
kids under 4
adolescent males
lymphoblasts have ___ chromatin
thin
the same kind of B cell causes ___ and ___
small lymphocytic ly
CLL
___ is always positive for neoplastic cells in ___, and usually in ___.
BM
CLL
SLLy
___s are vague nodular areas with large cells with prominent nucleolus, characteristic of ___
proliferation center
CLL/SLLy
CLL/SLLy (naive B cell) phenotype (4)
CD5
CD20 (weak)
CD23
CD43
10% of CLL/SLLy transform to ___. the switch is called ___.
DLBCLy
Richter's syndrome
translocation for MCL
it is not completely ___ for MCL
the effect is ___.
t(11;14)
specific
upregulation of cyclin D1 (Bcl-1)
MCLy cells are ___ sized with ___ nuclei, ___ nucleoli and ___ cytoplasm
small-medium
irregular
small
scant
in MCLy follicles are ___
absent
MCLy phenotype
CD5
CD20
CD43
Bcl-1
FLy follicles lack ___.
___ are always present between FLy follicles
mantle zone
neoplastic cells
translocation for FLy
this causes ___
the effect is ___.
t(14;18)
overexpression of Bcl-2
prevention of apoptosis
T/F: prognosis for FLy is worse with t(14;18)
false
2 kinds of cells in FLy
centrocyte
centroblast
centrocyte is aka ___
centroblast is aka ___
small cleaved follicular center cell (FCC)
large non-cleaved FCC
phenotype of FLy (germinal center) cells (4)
CD20
CD10
Bcl-2
Bcl-6
centrocytes are more ___ and centroblasts are more ___ and have ___
purple
pink
prominent nucleolus
grade 1 FLy is ___ (2)
grade 3 FLy is ___ (2)
indolent
incurable
aggressive
curable with chemo
grade 1 FLy can transform to ___ (2)
grade 3 FLy
DLBCLy
MZLy and maltoma have ___ nuclei and ___ cytoplasm. they are caused by ___ cells
irregular
clear
marginal memory (post-germinal-center) B cells
4 stages of MZLy
infiltration around follicles
follicular colonization
diffuse infiltrate
invasion of surrounding epithelium
3 diseases caused by marginal memory B cell
MZLy
splenic MZLy
extra-nodal MZLy
extra-nodal MZLy is aka
MALToma
phenotype of marginal memory B cell (3)
CD20
CD79a
CD43+/-
MALTomas are commonly caused by inflammation caused by ___ (3)
H. pylori
B. burgdorferi
autoimmune disease
T/F: treating causative infection can cure the MALToma
true
small B Lys with CD5-, CD10+
FLy
small B Lys with CD5+, CD10-
CLL/SLLy
MCLy
small B Lys with CD5-, CD10-
MZLy
although both are CD5+, CD10-, CLL/SLLy are ___ whereas MCLy is ___.
CD23+
Bcl-1+
in DLBCLy, nucleus is at least ___ the size of ___
twice
normal lymphocyte
in DLBCLy, ___ is most common site of extranodal involvement
GIT
DLBCLy has ___ markers with initial phenotype ___ (3), and eventually with ___ (3) also.
mature B cell
CD19
CD20
CD79a
CD10
Bcl-2
Bcl-6
translocation in Burkitt's ly
this causes ___
t(8;14)
overexpression of c-MYC (chromosome 8) by Ig promoter (chromosome 14)
in locations such as ___ where BLy is endemic, ___ is present in tumor cells
africa
EBV DNA
BLy has ___ appearance with interspersed ___s
starry sky
tingible body MQ
plasma cell monoclonality can be dx if ___ ratio isn't approximately ___
kappa/lambda
3
plasma cell phenotype
CD38
CD138
___ is a morphological variant of a plasma cell
Mott cell
T/F: MM cells generally have normal morphology
true
___ morphology and ___ are associated with bad MM prognosis
plasmablastic
high Ki67 index
plasmablasts look like ___ cells
DLBCLy
MM prognosis is based mostly on ___
BM infiltration
dx of MM requires ___% BM plasmacytosis
>30
___ is a plasma cell tumor without systemic effects
plasmacytoma
2 kinds of plasmacytoma
solitary p of bone
extraosseous p
3 most common sites for solitary plasmacytoma of bone
___% develop MM within 10 years
vertebrae
ribs
skull
55
most common site for extraosseous plasmacytoma
MM is common/rare
respiratory tract
rare
most common T-cell ly
peripheral T cell ly, unspecified
2 kinds of anaplastic large cell ly
ALK+
ALK-
most ALCLy is ALK ___
positive
ALK is a ___ produced by ___
Y kinase
translocation
___ (2) are skin conditions caused by T cell tumors. the cells have irregular ___ nuclei, and cause ___
Mycosis fungoides
Sezary syndrome
cerebriform
Pautrier microabcesses
phenotype of epidermotropic T cell
CD3
CD4
CD5
___ has leukemic syndrome with erythroderma
Sezary syndrome