1/55
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai | Chat |
|---|
No analytics yet
Send a link to your students to track their progress
this disorder of development causes supernumerary nipples that can extend from the axilla to the perineum
milk line remnants
this developmental disorder is from the ductal system extending into subcutaneous tissue or axillary fossa
accessory breast tissue
this disorder occurs in the 1st month of breast feeding and is caused by a local infection with staph aureus. it can create an abscess, erythematous and painful breast
acute mastitis
this disorder causes a painful erythematous subareolar mass, seen in smokers, there is a presence of keratinizing squamous metaplasia of the nipple ducts which slough off and create an inflammatory response
squamous metaplasia of the lactiferous ducts
this disorder creates a palpable periareolar mass associated with white nipple secretions, is not associated with smoking, pain or erythema
duct ectasia
what disorder can duct ectasia mimic both clinically and radiographically
invasive carcinoma
this disorder forms after trauma or prior surgery and contains small chalky white foci within firm gray white nodules
fat necrosis
this term refers to lumpy bumpy breasts with densities with cysts on mammorgraphy
fibrocystic change
what are the 3 principle morphologic features of fibrocystic change?
cysts, fibrosis, adenosis
this disorder produces an increased number of both luminal and myoepithelial cell types which fill the ducts and lobules creating slit like fenestrations at the periphery
usual ductal hyperplasia
this disorder is characterized by an increased number of acini compressed by a dense stroma arranged in a swirling pattern with calcs in the lumens
sclerosing adenosis
this disorder mimics invasive carcinoma mammographically, grossly and histologically, contains a central nidus of small tubules entrapped by a fibrotic stroma that projects at the periphery with cyst formation
complex sclerosing lesion
this disorder is characterized by a growth within a dilated duct which is composed of multiple branching fibrovascular cores which arborize within the lumen. it is associated with nipple discharge
papilloma
this disorder is associated with a subareolar enlargement of male breasts with increased number of ducts with loose cellular stroma. no LOBULE formation
gynecomastia
this precursor lesion is associated with variably dilated acini lined by columnar epithelial cells producing microcalcs
columnar cell lesion
this precursor lesion is characterized by a a columnar cell lesion with cytologic atypia lacking architectural complexity
flat epithelial atypia
this precursor lesion shows proliferation of epithelial cells arranged in cribriform or micro papillary patterns resembling DCIS, the duct is partially involved by atypical epithelial proliferation
atypical ductal hyperplasia
this precursor lesion is neoplastic proliferation of dyscohesive epithelial cells confined to the ductal-lobular system with loosely cohesive cells partially filling a lobule. the cells do not extend >50% of the acini of the lobule
atypical lobular hyperplasia
DCIS is cahracterized by malignant clonal proliferation of epithelial cells limited to the ducts and lobules by the:
basement membrane
what is the mammography appearance of DCIS
linear branching pattern
this form of DCIS creates a cookie cutter pattern with spaces filled with calcified secretly material
cribriform
this form of DCIS creates a complex bulbous protrusion without a fibrovacular core
micropapillary
this form of DCIS creates true papillae with fibrovascular core and lacks a myoepithelial layer
papillary
what are two important clues for identification of DCIS
intraductal calcifications and comedo
this disease is characterized by cells extending from DCIS within the ductal system via the lactiferous sinuses into the nipple skin without crossing the BM still
paget disease
this carcinoma is characterized by malignant proliferation of epithelial cells within ducts and lobules growing discohesively
LCIS
what is there a loss of in LCIS?
E-cadherin
what is it called when LCIS spreads into adjacent lobule but still not involving the nipple or skin?
pagetoid spread
what is the most common and deadly malignancy in women?
invasive carcinoma of the breast
what gene mutations are associated with the low-grade pathway of invasive breast cancer
PIK3CA
what gene mutations are associated with the high grade pathway of invasive breast cancer
tp53, brca1/2, HER2
this invasive cancer type is well-differentiated, strong ER/PR +, with low proliferation and mutations in PIK3CA
luminal A
this invasive cancer type is more poorly differentiated with lower ER/PR expression, high proliferation rate, aggressive and frequently in patients with BRCA2 mutations
Luminal B
this invasive cancer is a subtype of cancer found in patients with li fraumeni syndrome from germline tp53 mutations
HER-2 carcinoma
this invasive cancer type arises through an estrogen independent pathway with the most commonly mutated gene being Tp53. It exhibits solid growth pattern with nuclear pleomorphism and necrosis with high proliferation
Triple negative breast cancer
what is the term for grading of invasive breast cancers using glandular differentiation, nuclear pleomorphism and mitotic rate
nottingham histologic score
this type of luminal breast cancer expresses a loss of e-cadherin with increased risk with loss of CDH1, metastasizes to peritoneum/retro, leptomeninges, go, ovaries, UT
lobular carcinoma
dyscohesive infiltrating tumor cells arranged in linear cores often with signet ring cells with minimal desmoplasia is characteristic of which luminal breast cancer subtype?
lobular carcinoma
this luminal breast cancer subtype is characterized by being soft, rubbery, with pale gray blue gelatin with pushing or circumscribed borders. histologically there cells are arranged in small islands with large lakes of mucin
mucinous carcinoma
this luminal carcinoma subtype consist of well formed tubules and is often mistaken for a benign sclerosing lesion
tubular carcinoma
this luminal carcinoma subtype produces true papillae with fronds of fibrovascular tissue lined by tumor cells
papillary carcinoma
this HER-2 carcinoma subtype resembles cells lining sweat glands with prominent nucleoli and eosinophilic cytoplasm
apocrine carcinoma
this HER-2 carcinoma subtype forms hollow balls of cells floating within an intercellular fluid which mimics true papillae with no fibrovascular core
invasive micropapillary carcinoma
this subtype of triple negative breast cancer displays tumors demonstrating squamous or mesenchymal differentiation with poor prognosis
metaplastic carcinoma
this triple negative breast cancer subtype displays round to oval tumor cells in microcytic or tubular patterns with intraluminal secretions
secretory carcinoma
how does inflammatory carcinoma travel in the breast to penetrate the skin
lymphovascular space
does a low PR expression or a strong PR expression have a better clinical outcome?
strong PR expression
what is the most important familial factor in male breast cancer
mutation in BRCA2
what are the majority of male breast cancers?
invasive cancer of no special type (ER/PR+, HER-2-)
what are the common mutations of intralobular stroma lesions
MED12 and RARA
what is the most common benign stromal tumor of the female breast
fibroadenoma
this interlobular tumor has mutations in MED12/RARA along with others like tp53, rb, TERT, presents in 6th decade, varies from small to massive lesions with leaflike growth and bulbous protrusions
phyllodes tumor
what is themes important predictor of local recurrence following excision of phyllodes tumors?
margin status
this interlobular stromal tumor is equally common in males, benign and composed of myofibroblasts
myofibroblastoma
this interlobular stromal tumor is malignant, can arise sporadically in younger women with a poor prognosis or be due to radiation therapy or lymphedema with MYC amplification
angiosarcoma
what cancer can be associated with breast implants due to chronic inflammation
anaplastic large T cell lymphoma