Borders of the Breast:
Superior: Clavicle
Medial: Lateral edge of the sternum
Inferior: Inframammary fold
Lateral: Medial edge of the latissimus dorsi
Borders of the Axilla:
Superior: Axillary vein
Deep: Serratus anterior muscle
Posterior: Subscapularis muscle
Inferior: Meeting of the latissimus dorsi and chest wall forming a triangular structure
Nerves at Risk:
Long thoracic nerve: Injury results in winged scapula
Thoracodorsal nerve: Injury results in weakness of should ADduction
Axillary Lymph Node Levels:
Level I: Lateral to the pectoralis minor
Level II: Posterior to the pectoralis minor
Level III: Medial to the pectoralis minor
During axillary node dissection for breast cancer, levels I and II should be removed, but it's not necessary to extend to level III.
Symptoms:
Inquire about any symptoms that prompted the visit
Masses: Note any changes in size, consistency, or cyclical nature related to the menstrual cycle
Nipple changes: including discharge or retraction
Skin changes: erythema, dimpling, etc
Risk Factors:
Age of first menarche and menopause
Age of first live birth
Breastfeeding history
Family history: Including breast, gynecologic, and ovarian cancers
Prior mammograms and biopsies: including results
Oral contraceptive use
Fertility treatments
Hormone replacement therapy
Estrogen exposure is a risk factor for breast cancer. Factors such as early menarche, late menopause, and hormone replacement therapy increase estrogen exposure, while multiple pregnancies and breastfeeding decrease exposure.
Risk Assessment Models
Gail Model: Used to calculate lifetime risk of breast cancer.
Physical Exam:
Perform both seated and supine
Inspection: Assess symmetry, skin changes, and nipple changes
Palpation: Systematically palpate for lumps or bumps, noting location, size, distance from the nipple, and quadrant.
Axillary exam: Always include axillary nodes; also consider supraclavicular and inframammary nodes.
Screening Mammography:
Standard Views: Craniocaudal (CC) and Mediolateral Oblique (MLO)
Guidelines: Start at age 40 for average-risk women; repeat annually
High-Risk Patients:
>20% lifetime risk (Gail model) or BRCA mutation: Annual MRI and mammogram, staggered every six months
Diagnostic Mammography:
Used for further investigation of abnormalities, with additional compression and magnification views
Concordance:
Ensure agreement between imaging, physical exam, and biopsy results; discordance may indicate sampling error and the need for repeat or excisional biopsy.
BI-RADS (Breast Imaging Reporting and Data System):
0: Technical limitation, needs repetition
1: Negative, no findings
2: Benign findings
3: Probably benign, short interval follow-up (6 months or less)
4: Suspicious, biopsy required
5: Very suspicious/probably malignant, biopsy required
6: Known malignancy (post-biopsy, pre-excision)
Symptoms: Pain, erythema, swelling
Association: Often related to lactation, common during breastfeeding, especially after the first child
Mastitis vs. Abscess:
Mastitis: Cellulitis-like, red, painful skin infection
Abscess: Fluid or purulent collection in addition to skin changes
Workup for Suspected Abscess: Ultrasound to detect fluid collection if no palpable fluctuation.
Common Bacteria: Staph aureus and streptococci
Treatment:
Early antibiotics (e.g., Augmentin), avoiding tetracyclines or Cipro
Supportive measures for mastitis: Compresses, supportive bras
Can continue breastfeeding.
Breast Abscesses: Aspiration preferred over incision and drainage (I&D) to minimize scarring; repeat aspiration if recurrence. I&D is indicated if aspiration fails.
Benign Features: Bilateral, milky, cyclical (hormonally related); green discharge (fibrocystic disease).
Concerning Features: Bloody or serous, unilateral, spontaneous, non-lactational, persistent. Requires workup with mammogram and ultrasound to rule out cancer
Intraductal Papilloma:
Most common cause of bloody nipple discharge
Treatment: Excision, often requiring localization via ductography
Characteristics: Benign, common in adolescents and young women, painless, slow-growing, rubbery, well-circumscribed, palpable mass.
Imaging: Ultrasound is preferred over mammogram due to dense breast tissue in younger patients. Findings are described as well circumscribed, regular borders.
Diagnosis: Ultrasound-guided biopsy is required to confirm.
Treatment: Excision if symptomatic, growing, or >3 cm.
Characteristics: Fibroepithelial tumor, grows larger than fibroadenomas, occurs in older adults. Histology shows leaf-like pattern, cleft-like spaces, hypercellular stroma.
Diagnosis: Core needle biopsy cannot determine if the tumor is benign or malignant. Diagnosis require excision.
Treatment: Excision with wider margins than fibroadenomas. No axillary surgery is needed.
Metastasis: Ten percent can be malignant and spread hematogenously, commonly to the lungs.
Presentation: Eczematous, scaly, red, or ulcerated bloody changes around the nipple; often mistaken for a skin rash.
Etiology: Malignant cells in the skin of the nipple.
Workup: Diagnostic mammography, ultrasound; MRI if initial imaging is negative.
Treatment: Treat the underlying malignancy (DCIS vs. invasive cancer), with excision of the nipple-areolar complex during surgery.
Description: Malignant cells confined to the duct lumen (stage 0 breast cancer).
Progression: Premalignant, 50% progress to invasive cancer.
Presentation: Usually presents as calcifications on screening mammogram.
Diagnosis: Core biopsy is essential for diagnosis and hormone receptor testing.
Treatment: Lumpectomy followed by radiation (standard) or mastectomy (for diffuse, multi-quadrant DCIS or contraindication to radiation).
Lumpecteomy requires 2mm negative margins
Axillary Surgery: Sentinel lymph node biopsy is not needed, as DCIS does not invade lymphatics.
Adjuvant Therapy: Endocrine therapy (e.g., Tamoxifen) is recommended if ER/PR positive.
Characteristics: Usually found incidentally, less associated with calcifications or masses, considered a marker of increased breast cancer risk (1% per year per breast).
Risk Implication: Increases the risk for both breasts, ductal carcinoma likely to come back.
Treatment: Complete excision to rule out other pathologies (e.g., DCIS), adjuvant endocrine therapy (prevention measure), high-risk screening, or prophylactic mastectomy in select cases.
Types: Ductal carcinoma (more common) and lobular carcinoma.
Staging: Based on TNM (Tumor, Node, Metastasis) system.
T1: Small tumors (≤2 cm).
T2: Tumors between 2cm and 5cm
T3: >5cm
T4: invading other structures (like pec)
N: Nodes assessed via axillary exam.
M: Distant metastases.
Workup: Physical exam (lymph nodes), diagnostic mammogram, ultrasound, core needle biopsy (grade, receptor status, HER2 status).
Presentation: Peau d'orange (skin erythema, dimpling, and thickening) due to dermal lymphatic invasion.
Diagnosis: Clinical diagnosis based on peau d'orange and swelling, confirmed by skin punch biopsy.
Imaging: Mammogram and ultrasound are primary; MRI is sometimes used in high-risk patients.
Treatment: Neoadjuvant chemotherapy, modified radical mastectomy (mastectomy with complete axillary lymph node dissection), and adjuvant radiation.
Breast-Conserving Therapy (Lumpectomy/Partial Mastectomy):
Excision of the tumor with a rim of normal tissue (no tumor on ink at margins).
Almost always includes radiation to reduce recurrence.
Mastectomy:
Complete removal of all breast tissue.
Radiation may not always be required.
Often combined with reconstruction modalities (tissue expander followed by implant or flap, e.g., DIEP flap).
Both options have the same overall survival rates; mastectomy has a slightly lower recurrence rate.
Sentinel Lymph Node Biopsy:
For clinically node-negative patients.
Uses radioactive tracer and blue dye to identify and excise the first draining lymph nodes.
Excise any palpable, blue, or hot nodes (uptaking >10% of maximum).
Axillary Lymph Node Dissection:
For inflammatory breast cancer or clinically node-positive patients.
Removal of all level I and II lymph nodes.
Indicated if nodes remain positive after neoadjuvant therapy or if sentinel lymph node biopsy is not feasible.
Chemotherapy:
Can be given neoadjuvant (before surgery) or adjuvant (after surgery).
Neoadjuvant chemotherapy is used for large tumors, clinically node-positive disease, skin/chest wall involvement, and aggressive histologies (triple-negative or HER2-positive).
HER2-positive cancers require HER2-directed targeted therapy (trastuzumab, pertuzumab).
Adjuvant chemotherapy may be indicated based on genomic risk factors (Oncotype DX score).
Radiation:
Local treatment to reduce recurrence after lumpectomy or mastectomy (depending on pathology).
Endocrine Therapy:
Selective Estrogen Receptor Modulators (SERMs): Tamoxifen for premenopausal, ER/PR-positive tumors, or chemo-prevention (LCIS).
Aromatase Inhibitors (Letrozole, Anastrazole): For postmenopausal patients.
Side effects: Hot flashes, joint pains, osteopenia (monitor with DEXA scans).
Goal: Administer endocrine therapy for approximately five years.