Chapter 33: Disorders of the Breast Flashcards

1
Q

How do hormones affect the breast tissue

A

Hormones: Estrogen is primarily responsible for the growth of adipose tissue and lactiferous ducts. Progesterone leads to lobular growth and alveolar budding.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

How often does breast pain/breast mass = cancer?

A

a. History: Breast pain and/or mass. Pay attention to this as the patient’s anxiety can be high. Only about 6% of evaluated breast symptoms are cancer.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

How helpful is a mammogram at detecting cancer?

A

i. Mammogram: Breast lesions 2 years before they become palpable. 4 shots, 2 craniocaudal and 2 medio-lateral. Evaluate for calcium, fibrocystic change, and distortion of normal architecture. Easier to detect ductal carcinoma than lobular.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Discuss BIRADs

A

Breast imaging reporting and data system)
a. 0 = need additional imaging due to nondiagnostic lesion
1 = negative
2 = benign
3 = Probably benign = F/u, most likely benign though
4a = Low suspicion = Needs intervention
4b = intermediate suspicion = Possible malignancy
4c = Moderate concern = No classic sign but malignancy expected
5 = highly suggestive
6 = Bx proven malignancy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

When do we use US vs MRI?

A

ii. US: Used in younger women with fibrocystic change or those with dense tissue to discern better detail. Less than 40 typically get this more than mammogram.
iii. MRI: Can’t detect microcalcifications and is $$$, but can show good detail otherwise. Good adjunct

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

FNA vs. core biopsy

A

iv. FNA Bx: Aspirate with 22-24 gauge needle. Fluid = cyst, return in 4-6 months for standard CBE. If reappears, return for diagnostic mammo or US. Bloody fluid needs to go for cytology with imediate diagnostic mammo and US
v. Core needle: Larger bore, 14-16 gauge, for larger solid masses. 3-6 2cm samples taken

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Three types of mastalgia

A
  1. Cyclic - Begins with luteal phase of menstrual cycle and resolves with onset of menses. Bilateral pain, often the upper quadrants
  2. Non cyclic - Not associated with cycle. Tumors, mastitis, cysts, history of breast surgery, medications like hormones, antidepressants, setraline and amitriptyline, antihypertensives, etc.
  3. Extramammary - Chest wall trauma, rib fractures, shingles, fibromyalgia. Give NSAIDs, r/o dangerous stuff like heart pthology
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Three options for treatment of mastalgia

A
  1. Danazol is the only one FDA approved for this use, lots of SEs.
  2. SERMs can help, like Tamoxifen. Estrogen antagonist, but increase endometrial hyperplasia and DVT, hot flashes, VB. Only give in severe mastalgia cases not helped by anything else. Raloxifen a bit better, does not stimulate endometrium
  3. Some with cyclic mastalgia have decrease in pain with oral contraceptives or the injectable medroxyprogesterone acetate
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Ductal ectasia and it’s link to nipple discharge

A

i. Usually benign but can be an early sign for bad stuff. Bilateral non-bloody often associated with fibrocystic change and ductal ectasia (ductal dilation with inflammation and fibrocystic changes). Can also see green, brown, or yellow

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Milky discharge =

A

ii. Milky = TCAs, oral contraceptives, lactation, hyperprolactinemia, hypothyroid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Bloody discharge and what we can do about it if we’re fancy

A

iii. Bloody + bilateral = invasive ductal, intraductal papilloma or intraductal carcinoma. Ductography to diagnose with potential excision. Fiberoptic ductoscopy allows visualization and biopsy (not very available)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Chances of a nonproliferative breast mass becoming cancer

A

Nonproliferative: No increased chance of developing invasive carcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

6 types of nonproliferative change

A
  1. Fibrocystic change - Fibrous change associated with ruptured cysts
  2. Cysts - Lobules grow and shrink, can fill with fluid
  3. Fibrosis - Firmness of breast
  4. Adenosis - Increased glands with growing lobules. No change in architecture of lobules.
  5. Lactational adenomas - Secondary to exaggerated hormone response
  6. Fibroadenomas - Round, solid, rubbery, mobile. Structural and glandular components. Can enlarge in pregnancy due to hormones and cause pain
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Proliferative without atypia increases our cancer risk by how much?

A

1.5 - 2.0x

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Types of proliferative but not atypical breast changes

A

Epithelial hyperplasia
Sclerosing adenosis
Complex sclerosing lesions
Pappillomas

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Epithelial hyperplasia is what exactly?

A
  1. Epithelial hyperplasia - More than the normal two layers of cells (myoepithelial and luminal)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Sclerosing adenosis vs complex sclerosing lesions

A
  1. Sclerosing Adenosis - Increasing fibrosis within an expanded lobule that compresses against epithelium
  2. Complex sclerosing lesions (radial scar) - Nidus of tubules entrapped in a densely hyalinized stroma surrounded by radiating arms of epithelium. Mimics invasive carcinoma
18
Q

What are papillomas?

A
  1. Papillomas - Intraductal growths composed of abundant stroma lined by both luminal and myoepithelial cells. Can lead to serous or serosanguinous drainage in women aged 30-50 years
19
Q

When we think atypical proliferation, what is happening? How much of an increased chance of cancer is there?

A

Proliferative with atypia = 8-10x increased risk. When malignant cells replace the normal epithelium lining the ducts or lobules, the lesion is known as a carcinoma in situ. Basement membrane remains intact.

20
Q

LCIS vs DCIS and what we do about them

A
  1. LCIS - uniform small atypical cells obliterating glandular acini
    a. Excisional biopsy. Preventative therapy with SERMs like Tamoxifen in order to reduce the risk of invasive breast cancer
  2. DCIS - Epithelial cell atypical proliferation
    a. Core needle biopsy followed by surgical biopsy or excision. Prevent therapy like with LCIS.
21
Q

How common is breast cancer?

A
  1. Breast Cancer: Second most common malignancy in women, ranking only behind skin cancer. Also second leading cause of death in women cancer related. Lifetime risk is 1/8 (12%) with lifetime risk of dying is 3.6%
22
Q

Most important risk factor for breast cancer?

A

Age, most over 50

23
Q

6 other important risk factors to know besides age

A

i. Menarche before age 12
ii. Menopause after 55
iii. > 20cGy radiation (0.3 in a mammogram), takes 5-10 years after high dose exposure
iv. Firmer breasts
v. Overweight after menopause
vi. Women who drink 2-4 alcoholic drinks per week are at 30% greater risk of dying of breast cancer than women who never drink.

24
Q

BRCA1 vs BRCA 2

A

b. Genetics: BRCA 1 on 17q21. Associated with half of early-onset breast cancers and 90% of hereditary ovarian cancers. BRCA 2 on 13q12-13 has lower incidence of early onset breast cancer and much lower risk of ovarian cancer.

25
Q

What is the gail model and what are the limitations?

A

i. Gail Model: Calculates risk of getting breast cancer in the next 5 years and lifetime risk. Seven risk factors: History of LCIS or DCIS, age, menarche age, age of first birth, number of first degree relatives with breast cancer, history of breast biopsy, and race/ethnicity.

Falsely increased in women who have had multiple biopsies and less useful for those with second degree contacts. This tool, unlike reality, uses family history as the leading risk factor (recall that age is the leading risk factor).

26
Q

What is a “poor” outcome with the Gail model and what can we do with it?

A
  1. Women at “high risk” (1.7%+ chance in 5 years) referred for prophylactic therapy via SERMs (Tamoxifen, Raloxifene) and prophylactic mastectomy
27
Q

Commonality and behavior of invasive ductal vs invasive lobular

A

ii. 70-80% are invasive ductal. Cannot lead to lobular. Unilateral, unicentric and only the ipsilateral breast.
iii. 5-15% are invasive lobular, multifocal and bilateral, can spread to become ductal and/or more lobular.

28
Q

To define as a cancer as stage 1 or 2, what are the limits?

A

Up to 5cm

0-3 nodes involved

NO METS

29
Q

Stage 3 of breast cancer

A

Locally advanced.

Basically any number of local nodes affected without metastasis, size can be larger than 5cm.

30
Q

Stage 4 of breast cancer

A

Distant metastasis

31
Q

Surgery options for breast cancer

A

i. Surgery: Lumpectomy with radiation, mastectomy, modified radical mastectomy (axillary nodes) and don’t forget SLNBx. Tissue expanders and reconstructive therapy great for image.

32
Q

Adjuvant medical therapy for breast cancer

A
  1. Adjuvant systemic therapy for all breast cancer regardless of LN status. Chemo to kill cells and tamoxifen to prevent estrogen acting to cause more cancer (ER+) and for 5 years post-op.
33
Q

Talk about aromatase inhibitors

A

Aromatase inhibitors - Prevent production of estrogen in women. Extend survival in metastatic women and act as primary adjuvant therapy, in conjunction with tamoxifen to reduce recurrence rate

34
Q

When do we use Trastuzumab?

A

Trastuzumab against Her2/neu. SE: Heart failure, respiratory problems, life threatening allergic reactions

35
Q

How do we follow women after treatment for breast cancer

A

Every 3-6 months for first 2 years. Annually after that. Most re-occurrences occur within first 5 years

36
Q

Breast cancer screening review

A

Screening: Breast self-awareness in low risk patients and breast self exams in high risk.

CBEs every 1-3 years from 20-39, annually thereafter. Mammography annually after 40, or 50 with your decision from 40-50. Nothing after 75.

If Genetic issues, monthly BSEs from 18-20, annual CBEs, screening mammograms after 25 or 5-10 years before the age of diagnosis of affected relative.

37
Q

How do we treat stage 0 cancer?

A

BCT or mastectomy. No adjuvant therapy needed unless using radiation with BCT

38
Q

How do we treat stage 1 cancer?

A

BCT or mastectomy. Chemotherapy if >2cm, consider tamoxifen. Consider SLnBx.

39
Q

How do we treat stage 2 cancer?

A

Modified radical or BCT with axillary LN dissection if indicated. Chemo if greater than 1 cm, again consider tamoxifen as well. Radiation of supraclavicular nodes, consider chest wall, if mastectomy performed and/or 4+ affected LNs

40
Q

Stage 3 treatment

A

Same as Stage 2 as far as surgery. If inflammatory breast cancer, radiation to breast.

41
Q

Stage 4 treatment

A

Surgery for local control, chemotherapy, consider hormones