mutation in flat epithelial atypia, LG DCIS, ADH, lobular
deletion of ch 16q
cystic neutrophilic granulomatous mastitis
Corynebacterium
lymphocytic mastopath/sclerosi na lymphocytic lobulitis
DM type 1 female
function of BRCA 1/2
tumor suppressor genes
HER2 amplification in what chromosome
17q
Luminal pathway
BRCA2 - 1q gain, 16q loss - FEA - PIK3CA - ADH - DCIS - ER positive, HER2 neg
HER2 positive pathway
TP53, HER2 amp - DCIS - HER2 positive
Basal/TNBC pathway
BRCA1 mutation, TP53 - BRCA1 inactivation - DCIS - TNBC
HER2 IHC stain in Paget cells
positive
mutation in male breast CA
BRCA2
additional mutation in malignant phyllodes
TERT
mutation in HG DCIS
17q loss
ETV6-NTRK3 mutations
secretory CA
infantile fibrosarcoma
cellular variant congenital mesoblastic nephroma
mitotic count field diameters for
0.44
0.59
0.63
6-10
10-19
12-22
post-radiation angiosarcoma mutation
MYC
masson tumor
intravascular papillary endothelial hyperplasia