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