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56 Cards in this Set

  • Front
  • Back
em of melanosome
melanosome 4 stages- stage 2 - can tell it's a melanosome, stage 3 with pigmentation
elongated football shaped structure with lines in cytoplasm
blue nevus
pigmented lesion spares epidermis, involves superficial dermis, heavily pigmented dendritic melanocytes (long, wavy)
increased fibroblasts and thicker collagen - NO EPIDERMAL INVOLVEMENT
hmb45 is positive
cellular blue nevus
children, lumbosacrum, dumbbell shaped, bullous base
cells that pigmented wavy dendritic melanocytes
islands of spindled/epithelioid (pale abundant cyto, little to no pigment)
macrophages in background
NO EPIDERMAL INVOLVEMENT
deep penetrating nevus, plexiform spindle cell nevus
bulky melanocytic lesion; occurs in upper back, shoulder
wedge-shaped
fascicles/plexiform of spindle-epitheloid abundant, finely pigmented cytoplasm
macrophages
no or few mits
abc cells of nevus
A - epitheloid (most superficial)
B - lymphocyte
C - neural cells
Spitz nevus (spindle and epitheloid cell nevus)
children most commonly
low mag - symmetric
epidermal hyperplasia
nests in junction (vertical orientation, bunch of bananas)
cells disperse as single cells at base
High mag up near junction - kimono bodies (eosinophilic lobules of BM material - right beneath epidermis), large nuclei, prominent nucleoli (smooth contours, fine chromatin), cytoplasm - amphophilic, delicate
can have pagetoid spread, focally, groups, in center
what benign pigmented lesions can have pagetoid spread
spitz nevus
acral nevus
recurrent nevus
congenital nevus
melanoma SS types limited set of fx
pagetoid spread (even into corneum), diffuse
no maturation
four types of melanomas
lentigo maligna - face, elderly, sun-damaged skin; if invasive spindled or desmoplastic, can run down hair follicle
SS - 70%, nests and single
acral/mucosal/lentingous type - pigmented lesion with increase of continguous DE junction
nodular melanoma - no epidermal component
radial growth phase
in situ vs non tumorogenic
vertical growth phase
large in dermis is larger than any nest in epidermal or any dermal mits
how know on face
increased sebacous elements
b cell lymphoma how to distinguish between melanoma and lymphoma
b cell lymphoma - bottom heavy, bulky, spares epidermis, diffuse blue, no follicle formation
primary and secondary forms
nodular melanoma vs. lymphoma - high mag and look for pigment, look more superficially for that pigment
look for DE junction component
what
what
steatocystoma (multiplex)
epithelial lined cyst with no granular layer, corregated eosinophilic lining
what
what
warty dyskeratoma (like darier's but isolated and centered on H&N, genital)
solitary lesion, face, cup-shaped invagination, filled with keratin, corrons, corgrains
large cells with ample cytoplasm, prominent nucleoli, large nuclei, all layers, compress adjacent keratinocytes
paget's - do ihc
extramammary pagets
primary, originates from apocrine glands at those sites, vulva, anogenital (less associated with underlying neoplasm)
what
what
circumscribed, dermis, two cell types, basophilic (matrical), ghosts cells (shadow cells), FBGCrxn, calcium
pilomatricoma
sebaceous adenoma
sebaceous adenoma
well-circumscribed, lobular, uniform sebaceous cells, nucleus can be scalloped, not assoc with follicle
two cells: peripheral basaloid cells, mature sebaceous cells (if adenoma 50% sebacous; if sebaceous epithelioma more of the peripheral cells; if carcinoma, on eyelid, aggressive)
what is assoc with muir torre syndrome
sebaecous carcinoma, while carcinoma less aggressive than sporadic
nevus sebaceous
nevus sebaceous
abortive hair follicles, epidermal hyperplasia, sebaceous hyperplasia, ectopic apocrine gland formaiton
most common b9 and malign neoplasms to develop within nevus sebaceous
syringocytoadenoma papillerfum
bcc
hidradenoma papilleferum
females, genital/vulvar
circumscribed, papillary, one-two cell layers, no connection to overlying epidermis, apocrine decapitation secretion
what
what
papillary, connects to epidermis, packed with plasma cells, apocrine decap secretion
scalp, face
syringocystadenoma papillerfum
what
what
pieces of jigsaw puzzle, two cell types, darker peripheral cells, central pink cells, basement lamina-material
tubular lumina (eccrine origin)
cylindroma
??
like cylindroma: two cell types, darker peripheral cells, central pink cells, basement lamina-material
tubular lumina (eccrine origin)
but anatomosing cords
syringoma
syringoma
tadpole lesions, epithelial cells with tails
dense collagen background
protein debris (sweat jello)
mac
follicular/eccrine differentiation (latter at base)
deep infiltrative
what
what
epidermal hyperplasia, elongation of rete ridges and basal hyperpigmentation (dirty fingers), grenz zone, spindle cell proliferation, entrapment of keloidal fibers
dermatofibroma
ihc for dermatofibroma
13a + cd34-
dfsp
dfsp
infiltrative, spindle cells, honeycomb of fat, storiform
ihc of dfsp
13a-, cd34+
what
what
similar ihc to dfsp, in kids, vascular like spaces, multilobated cells
giant cell fibroblastoma (juvenile counterpart to dfsp)
what
what
elderly, exophytic, ulcerated, atypical pleomorphic cells, high mits
AFX
"mfh is a deeper form of"
AFX
what
what
epidermal hyperplasia, dilated spaces right up to epidermis, protein debris (lymph fluid)
lymphangioma circumscriptum
what, ass/w
what, ass/w
dilated spaces with blood abut epidermis
angiokeratoma
fabry's
what, a/w
what, a/w
associated with Castlemans
glomeruloid hemangioma
kaposi's sarcoma - evolution
increased in slit-like vascular spaces, increased dermal spindle cells, promitory sign
spindle cells proliferative, hyaline globules
nodular formation with loss of vascular proliferation
four flavors of kaposi's
-all HHV8 associated
- aids associated one, visceral more common
angiosarcoma
vascular spaces, atypical cells
three clinical settings for angiosarcoma
1. elderly, white
2. chronic lymphadema (stuart-treves)
3. irradiated sites
glomus tumor
uniform round cells
HAND glomus body is a modified smooth muscle cell
solid form
if thin walled vessels (glomangioma)
if smooth muscle glomangiomyoma
ihc for spindle cell lipoma
cd34 +
sites of granular cell tumor
tongue, skin
merkel cell
skin, elderly, extremities
neuroendocrine chromatin pattern with little cytoplasm, molding
dot perinuclear staining of CK20
gorlin's syndrome
basal cell syndrome
AD
patched, czome 9
numerous basal cell carcinomas
associations: OKCs, palmar pits, rib abnormalities, medulloblastomas, calcificaiton of falx
muir torre syndrome
AD
HNPCC MSI mlh1 msh2
sebaceous tumors, colon, gu, endometrial tumor
burk hogg dube
AD
renal tumor/oncocytic, pulmonary cysts
cowden
AD
czome 10
trichellommas, breast and thyroid
gardners
AD
czome 5 apc
EICs, osteomas, polyps, desmoid tumors
Peutz jeghers
pigmented macules lips
hamartomatous polyps, colon carcinoma
TS
AD
two proteins:
angiofibromas (adenoma sebaceum),
cns hamartomas, subependymal
angiomyolipoma, etc
NF1
pheo
cerebral, a/w
cerebral, a/w
pheo
cerebral hemangioblastomas
skin: angiomatosis
vhl
men 2b
ret gene, pheochromocytoma