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91 Cards in this Set

  • Front
  • Back
good ihc markers for nerve sheath tumors (general)
S100, CD34, NFP, GFAP, EMA
what histochemical stain can be used for alveolar soft parts sarcoma
pas for crystals
stains for epithelioid sarcoma
Keratin, EMA, Vimentin, CD34
ihc for synovial sarcoma
Keratins, CK7, EMA
ihc for clear cell sarcoma
HMB45 >S100 protein
ihc fo4 Angiomatoid (Malignant) Fibrous
Histocytoma
50% desmin
three fx for grading sarcomas
Differentiation
Mitotic activity
Necrosis
examples of some grade 2 sarcomas
MFH, myxoid sarcomas, MPNST, and
angiosarcoma
of soft tissue sarcomas which are generally hematogenous
i hope i got this right
epitheloid and melanocytic (most others go to LNs)?
which sarcomas are not staged
Angiosarcoma, DFSP, IMFT, desmoid, and
sarcoma of parenchymal organs
primary stage determinant in sarcoma
tumor size
for treatment, when do more than just surgery
i believe usually when you get to intermediate, then employ rad/chemo
ihc for sarcomatoid scca
AE1/AE3, Keratin (CK) 5/6, p63
IHC for spindle cell adenoca
AE1/AE3, CK18 alone
if see dirty necrosis and cherry red nuclei, these are fx of what 2 general categories
carcinoma, melanoma
ihc for DLBL
CD20, CD79a, CD10, Bcl6, Bcl2
ihc for anaplastic large cell lymphoma
CD30, ALK-1, EMA
what
what
analplastic large cell lymphoma: dishesive and hallmark cells
what in lymphoma
what in lymphoma
dot and membrane staining with CD30 in anaplastic large cell lymphoma
ihc of MFH:
vimentin, focal S MA or MSA only,
diagnosis of exclusion
ihc of Liposarcoma:
S100 in lipoblasts, CD34 in
spindled cells
ihc of Rhabdomyosarcoma:
Desmin, MSA, MyoD1, myf4 (skeletal muscle specific
myogenin)
ihc of Leiomyosarcoma
: Desmin, SMA, MSA
ihc of Epithelioid Malignant Peripheral Nerve
Sheath Tumor
S100 protein, GFAP
five patterns of MFH
• Pleomorphic Sarcoma NOS (Storiform-
Pleomorphic MFH)
• Myxofibrosarcoma (Myxoid MFH)
• Giant Cell Rich
• Angiomatoid (Malignant) Fibrous
Histiocytoma
most common type of MFH
storiform/pleomorphic (90% are deep, intramuscular)
in whom does angiomatoid MFH occur
kids
what
what
pleomorphic/storiform MFH
if subcutaneous MFH usually what type
myxoid MFH
role of CD68 and CD163 in MFH
CD68 stains lots of mesenchymal cells, relatively nonspecific, stains cells with lysosomes
CD163 specific histiocyte marker, MFH cells are negative
what, where located
what, where located
50% myxoid histology, extremities, superficial location
what
what
myxofibrosarcoma - Prominent ropy vasculature “dripping” with tumor cells
another name for low grade fibromyxoid sarcoma
EVANS TUMOR, ON SPECTRUM
WITH HYALINIZING SPINDLE CELL
TUMOR WITH GIANT ROSETTES)
cytogenetic findings in fibromyxoid sarcoma
t(7;16)(q33;p11) FUS/CREB3L2
what
what
low grade fibromyxoid sarcoma
what
what
Hyalinizing Spindle Cell
Tumor with Giant Rosettes (on spectrum with low grade fibromyxoid sarcoma)
what
what
GC rich MFH
=storiform/pleomorphic MFH+ osteoclast-like GCs
what, ddx
what, ddx
inflammatory MFH: retroperitoneal, CD30+, CD15-
sheets of polys and xanthoma cells
clinically: systemic fx b sx, peripheral eos.
ddx: dediff liposarcoma, Hodgkin dz
how do sarcomas usually met
hematogenously
what
what
atypical fibroxanthoma
Solar Elastosis
Small size <1-2 cm and
Superficial dermal location:
cf pleomorphic liposarcoma from dedifferentiated liposarcoma
pleomorphic is just that - crazy cells
dedifferentiated floret-like GCs
ST leiomyosarcoma - mits
low tolerance for mits; cyto atypia with 1 mit/50 malignant involving cutaneous/dermis
pilar, angio or genital are exceptions
cytogenetics with pleomorphic rhabdomyosarcoma
CHOP
age group for pleomorphic rhabdomyosarcoma, ihc
>40 years, if mismatch between smooth muscle tumors, think skeletal
two pleomorphic sarcomas with worst prognoses
Pleomorphic Leiomyosarcoma
AND
Pleomorphic Rhabdomyosarcoma
ddx for fascicular malignant spindle cell tumors
“Fibrosarcoma”
Malignant peripheral nerve sheath tumor
(MPNST)
Synovial sarcoma
Kaposi sarcoma
if see a "fibrosarcoma" close to dermis, what is it
DFSP
"fibrosarcomas" have been stratified into what four tumors
Sclerosing epithelioid fibrosarcoma
Myxofibrosarcoma
Low grade fibromyxoid sarcoma
(Evans Tumor)
Fibrosarcoma arising in
Dermatofibrosarcoma Protuberans
DERMATOFIBROSARCOMA PROTUBERANS - in whom, where found, marker
males, Old Fashioned Bathing-Suit Distribution, pdgf-beta
some growth patterns for dfsp
honeycomb, storiform
ihc for dfsp
cd34 - goes away if portion develops into Fibrosarcoma (which is present portends a worse prognosis)
cytogenetics of DFSP
Ring chromosome: COL1A1-PDGFB fusion t(17;22)(q22;q13)
S100 and MPNST
if spindled (which most are), only focal S100. If epitheloid very S100.
those that arise in NF1 are spindled
what
what
MPNST - note nerve on side
what, ddx
what, ddx
MPNST,
can see donut growth (geographic necrosis/not dirty though) in syn sarc and PNETs too
what
what
MPNST+rhabdo=malignant triton tumor
what
what
syn sarcoma (biphasic)
what, CD7+, ema+, CD34-, czome?
what, CD7+, ema+, CD34-, czome?
monphasic synovial sarcoma t(x;18), SYT-SSX fusion
four clinical settings for kaposi sarcoma
Classic (Chronic) - middle age, men, meditteran
AIDS related
Post-Transplant
Lymphadenopathic (african)
same histol. etc
what
what
kaposi
fascicles of
spindle cells, separated
by slit-like vascular
spaces containing
erythrocytes, PAS
positive diastase
resistant hyaline
globules, extravasated
RBCs, scattered plasma
cells, and hemosiderin
deposits
breakdown of rbcs, hyaline globules, like pink grapes, think mediterrean
name 4 benign fascicular tumors
Fibrous Histiocytoma
Fibromatosis
Neurofibroma
Schwannoma
what
what
benign fibrous histiocytoma - note pushing stellate border
ihc for deep fibromatosis, syndromic assoc, gene alterations
nuclear beta catenin, apc, gardners (and sporadic)
what, ihc
what, ihc
Neurofibroma, note how central portion is more cellular, S100, CD34
name, dz
name, dz
wagner meisser corposcle
diffuse nf
skin findings of NF1
Café-au-lait macules appear
shortly after birth
lisch nodules, axillary freckle and neurofibromas occur in childhood or at puberty
findings in NF1 (not skin)
Neurofibromas
Optic glioma (pilocytic astrocytoma)
Bone changes: osteoporosis, kyphoscoliosis, and pseudoarthrosis (tibia)
Vasculopathy: arterial dysplasia, spontaneous rupture (renal, cerebral vessels)
mutation in NF1
loss of neurofibromin Nf1 (generally
suppresses Ras), chromosome 17, Tumor
Suppressor Gene
what
what
schwannoma
what
what
hyaline vascularization in antoni B (myxoid area) of Schwannoma
what
what
pericapsular lymphoid cuffing in cellular schwannoma
ihc for schwannoma
- S100 protein diffuse
– CD34 only in Antoni B
– EMA at periphery in capsule
(perineurium)
– Cellular schwannoma has diffuse S100
protein, GFAP, and occasionally keratin
reactivity
what
what
Madelung Lipomatosis, posterior shoulder, can be assoc with etoh
cytogenetic changes in spindle cell lipoma/pleomorphic lipoma
13q changes and 16q
losses with partial monosomy
what
what
chondroid lipoma
kidney, ihc, syndrome
kidney, ihc, syndrome
histo: thick walled vessels, 2) immature specialised smooth muscle cells which may be pleomorphic , 3)mature fat
ihc: desmin, HMB45
syndrome: TS
what
what
myxoid liposarcoma, plexiform vessels, t(12;16)
what, cytogenetics
what, cytogenetics
round cell liposarcoma, t(12;16), CHOP by FISH
Mesenchymal chondrosarcoma ihc
SOX9
Evans low grade fibromyxoid sarcoma FISH
FUS
ihc for ewings
vimentin, keratins, CD99, glycogen
pnet same but add in neural markers or EM
name 4 ish tumors that have the t(12;22)(q13;q12)
EWS-ATF1 fusion finding
Ewings/PNET
angiomatoid MFH
clear cell sarcoma
name 4 ish tumors with the same t(12;15)(p13;q25) ETV6-NTRK3 fusion
Infantile fibrosarcoma
Congenital mesoblastic nephroma
Acute myeloid leukemia
Secretory breast carcinoma
name two tumors with t(X;17)(p11.2;q25)ASPL-TFE3 fusion
Alveolar soft part sarcoma
Papillary renal cell carcinoma
two mutations in syn sarcoma
t(2;13)(q35;q14)
– PAX3-FKRH
t(1;13)(p36;q14)
– PAX7-FKRH
what
what
Nodular fasciitis;
MYXOID DEGENERATION
EXTRAVASATED ERYTHROCYTES AND
LYMPHOCYTES
honeycomb pattern in subcutis
DFSP
Neurofibroma
cf diffuse NF vs. DFSP
cd34 in both
s100 negat in dfsp, S100 pos in nf
look for weigner-m. corpusles in diffuse nf
see keloidal collagen think:
Keloid
nodular
fasciitis
fibromatosis,
see central necrosis think:
Epithelioid Sarcoma
Necrobiotic Granuloma (CD163, CD68 positive, negative for keratin, EMA)
Diabetic Lipoidica,
Rheumatoid Nodule,
Infection,
Granuloma Annulare
see extravascated rbcs, think:
Nodular fasciitis
Myxoid desmoid
Kaposi Sarcoma