Breast Disorders Flashcards

1
Q

Structure of a terminal ductule-lobular unit

A
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2
Q

TDLU histology

A
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3
Q

Breast cysts

A
  • Non-proliferative breast mass
  • Common in women ages 30-50
  • Round or ovoid in shape
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4
Q

Fibrocystic change

A
  • Nonproliferative breast mass
  • VERY common
  • Cycic pain and nodularity with menstrual cycle
  • Histology shown below
    • Dilation of ducts and acini
    • Dense stroma
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5
Q

Benign proliferative breast lesions without atypia

A
  • Intraductal papilloma
  • Fibroadenoma
  • Usual ductal hyperplasia
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6
Q

Intraductal papilloma

A
  • Benign proliferative breast lesion w/o atypia
  • Usually found ~2 cm from nipple
  • Assocaited with bloody or serous nipple discharge
  • Histology shown below
    • Proliferation of epithelial cells w/in the duct
    • Fibrous stalk usually present
  • Surgical excision recommended
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7
Q

Fibroadenoma

A
  • Benign proliferative breast lesion w/o atypia
  • Common in ages 15-35
  • Well-defined, mobile mass
  • Histology shown below
    • VERY dense stroma
    • Compressed ducts
    • Well circumscribed by normal breast tissue
  • May be observed or surgically excised
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8
Q

Usual ductal hyperplasia

A
  • Benign prolfierative breast lesion without atypia
  • Retain usual cytologic features of benign cells
  • No treatment needed
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9
Q

Benign proliferative breast lesions with atypia

A
  • Atypical ductal hyperplasia
  • Atypical lobular hyperplasia
  • Lobular carcinoma-in-situ
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10
Q

Atypical ductal hyperplasia

A
  • Beingn proliferative breast lesion w/ atypia
  • < 0.2 cm in size
  • Takes up part of, but not the entirety, of the duct (unlike DCIS)
  • Surgical excission recommended to prevent progression to DCIS (10% of cases)
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11
Q

Atypical lobular hyperplasia

A
  • Benign proliferative breast lesion w/ atypia
  • <50% of acini involved
  • Slight breast distension
  • Can be treated w/ observation since rate of progression is fairly low
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12
Q

Lobular carcinoma-in-situ

A
  • Benign proliferative breast lesion w/ atypia
  • Greater extent of disease than ALH w/ higher risk of progression
  • Nuclear grade usually low
  • Homogenous cells that are “discohesive” (loosely arranged)
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13
Q

Ductal carcinoma-in-situ

A
  • Malignant breast lesion
  • Cells fill the ducts without invading through the basement membrane
  • May be low nuclear grade and homogeneous, or high nuclear grade and heterogeneous
  • Cohesive, unlike the discohesive lobular carcinoma-in-situ
  • Comedo necrosis (shown below) is when there is a central necrotic core within the DCIS
    • This increases risk of invasion and of recurrence
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14
Q

DCIS vs LCIS histology

A

A is DCIS, B is LCIS

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15
Q

DCIS is sometimes referred to as. . .

A

. . . “stage 0” breast cancer

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16
Q

Clinical diagnosis and management of DCIS

A
  • Microcalcifications on mammogram are suggestive of DCIS
  • Treatment is with surgical excision (lumpectomy)
  • Frequent followup due to high risk of progression to invasive breast cancer
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17
Q

Major prognostication and treatment factors for invasive breast cancer

A
  • Hormone receptor status
  • Nuclear grade
  • Her2/neu expression
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18
Q

HER2/neu and Estrogen receptor positive cancers have a ___ prognosis

A

HER2/neu and Estrogen receptor positive cancers have a good prognosis

We can treat them with targeted agents!

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19
Q

Lymphatics of the breast

A
20
Q

Invasive ductal carcinoma

A
  • Invasive malignancy
  • 80% of breast cancers
  • Often found with co-existing DCIS
  • Presents as a solitary, firm mass with poorly defined margins
  • Is often painless
21
Q

Invasive ductal carcinoma susceptibility

A

75% of ductal carcinoma is ER+

22
Q

Invasive lobular carcinoma

A
  • Invasive breast cancer
  • 15% of invasive breast cancers
  • Forms “single file cords” on histology
23
Q

Invasive lobular carcinoma susceptibility

A

>90% ER+

24
Q

Types of invasive breast cancer

A
  • Invasive ductal carcinoma
  • Invasive lobular carcinoma
  • Inflammatory breast cancer
  • Paget disease of the nipple
25
Q

Paget disease of the nipple

A
  • Eczematous patch on the nipple
  • Associated with underlying DCIS or invasive ductal carcinoma
  • Intraepidermal proliferation of mammary-type epithelial cancer cells
26
Q

Distinctive cell morphology in Paget disease of the nipple

A
27
Q

Treatment of invasive breast cancer

A
  • Surgery:
    • Lumpectomy vs Mastectomy
  • Adjuvant therapy:
    • Radiation (for all, to reduce recurrence)
    • Hormonal therapy for 5 years (all ER+ tumors)
    • Chemotherapy (if high risk characteristics of tumor)
28
Q

When is the best time to perform a breast exam?

A

The follicular phase of the menstrual cycle

This is because there will be less secretory tissue or fibrocystic change at this time

29
Q

Sequence of evaluations of breast mass

A
  1. Breast exam and mammogram
  2. Ultrasound (if mammogram inconclusive)
  3. MRI (for women at extremely high risk of breast cancer, for example BRCA1 or 2 carriers)
30
Q

Cyclic mastalgia

A
  • Often involves luteal phase of the menstrual cycle
  • Pain often in outer quadrants of the breast
31
Q

Non-cyclic mastalgia

A
  • May be associated with antihypertensives, antidepressants, or hormone use
  • Potential causes:
    • Iatrogenic
    • Tumors
    • Cysts
    • Hx breast surgery
    • Mastitis
    • Idiopathic
32
Q

Approach to mastalgia should first start by differentiating. . .

A
  1. Cyclic mastalgia
  2. Non-cyclic mastalgia
  3. Chest wall pain (extra-mammary)
33
Q

Treatments for mastalgia

A
  • Behavioral:
    • Type fitting bra
    • Weight reduction
    • Regular exercise
  • Pharmacologic
    • Danazol (Androgen approved by FDA for treating cyclic mastalgia from fibrocystic change, but has significant side effects and should be second-line after behavioral therapy)
34
Q

Approach to nipple discharge

A
  • Spontaneous or expressed?
  • Unilateral or bilateral?
  • Uniductal or multiductal?
  • Color?
  • Associated mass?
35
Q

Characteristics of benign nipple discharge

A
  • Non-spontaneous
  • Non-bloody
  • Green, yellow, or brown
  • Bilateral
36
Q

Characteristics of malignant nipple discharge

A
  • Bloody, unilateral discharge
  • With associated mass
37
Q

Patient presents with bloody, unilateral, uniductal breast discharge. No mass is palpable on exam. What is the next step in workup?

A

Ductography

38
Q

Characteristics of a breast mass that suggest malignancy

A
  • Size > 2 cm
  • Immobility
  • Poorly defined margins
  • Firmness
  • Overlying skin changes
  • Retraction or changes in nipple
  • Bloody nipple discharge
  • Ipsilateral axillary lymphadenopathy
39
Q

What do you do with a suspicious breast mass?

A

Core needle biopsy!!!

40
Q

Overview of breast masses

A
41
Q

Once you have your core needle biopsy of a breast mass, the next step is. . .

A
  • For nonproliferative and proliferative without atypia:
    • Monitoring, no treatment
  • For proliferative with atypia (aka ADH, ALH, or LCIS):
    • Surgical excision
    • If confirmed non-invasive by surgery, close surveillence, lifestyle and diet change, and possibly chemoprevention w/ SERM
    • If found to be invasive, chemotherapy and radiation
42
Q

In a young patient, ___ is usually peferred to ___ as an imaging modality

A

In a young patient, ultrasound is usually peferred to mammography as an imaging modality

Since breast tissue tends to be firm and dense on mammography

43
Q

Mammography in a breastfeeding woman

A

All of the breast milk can make imaging poorer quality!

Have them pump just prior to your imaging.

44
Q

“Rubbery” breast mass

A

Buzzword for texture associated with fibroadenoma

Usually firm, nontender, rubbery masses, < 1 cm, that does not change with the menstrual cycle

A breast mass with benign features in a woman below age 25 is HIGHLY likely to be a fibroadenoma.

Confirm with FNA.

45
Q

___ is preferred to ___ as a biopsy modality for breast masses in patients with a low risk of breast cancer

A

Fine needle aspirate is preferred to core needle biopsy as a biopsy modality for breast masses in patients with a low risk of breast cancer

46
Q

Mammography schedule

A

Breast exams annually starting at age 40

Mammography annually starting at age 50 for no risk factors

Mammography annually starting at age 35 for FHx breast cancer