Breast Surgery JC076: Breast Mass: Breast Cancer, Benign Breast Diseases, Mammography, Breast Cancer Screening Flashcards

1
Q

Management of Breast disease

A

Triple assessment:
1. Clinical
- History + P/E
- S/S

  1. Radiological
    - Mammography
    - USG
    - MRI
  2. Pathological
    - FNAC
    - Core biopsy
    - Incisional biopsy
    - Excisional biopsy

—> Combined: sensitivity 99.6% + specificity 93%

  • Triple assessment is positive if ***ANY of above is positive
  • negative if ***ALL 3 negative
  • if findings not correlate —> further investigations / monitoring necessary
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2
Q

History taking of Breast disease

A
  1. HPI / Breast symptoms
    - **Lump
    - **
    Pain (Mastalgia)
    - ***Discharge from nipple (Unilateral / Bilateral, Single / Multiple ducts, Nature)
  2. Symptoms characterisation
    - **Duration
    - **
    Changes of symptoms (e.g. change with menstrual cycle, analgesia)
    - Unilateral / Bilateral
    - Characteristics (
    SSSTCM: Site, Size, Shape, Tenderness, Consistency, Mobility)
  3. Family history
    - 1st / 2nd degree
    - ***Age of onset (correlate with familial risks)
  4. ***Hormonal risk (esp. Steroid receptor +ve breast cancer)
    - Early menarche / Late menopause
    - Gestational history (Nulliparity)
    - Breast feeding history (↓ risk)
    - OC pills (exogenous estrogen)
    - Hormonal replacement therapy (exogenous estrogen)
  5. Previous breast disease / screening
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3
Q

P/E of Breast disease

A

Position + Exposure (at least clavicle to abdomen)

  1. Inspection (end of bed)
    - Asymmetry
    - Scar (esp. inframammary fold)
    - Mass
    - Skin changes
  2. Palpation (along clock face)
    - Breast mass
    - Nipple discharge
    - Axillary LN
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4
Q

Nipple discharge

A

Types:
1. Blood stained
- mostly pathological

  1. Serous
    - pathological / physiological
  2. Milky
    - lactation
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5
Q

Skin changes

A
  1. Eczematous change
    - scaling of skin + areola
    - if scaling / involvement of **nipple —> **Paget’s disease of nipple —> need incisional biopsy for Paget’s cells
  2. Peau d’orange
    - **skin tethering + **SC lymphedema changes —> associated with underlying cancer
    (from wiki: hair follicles become buried in edema)
  3. Inverted nipple
    - ask how long its been there
    - underlying tumour causing retraction of nipple
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6
Q

***DDx of Breast mass

A

Benign (Mobile, Round, Smooth):
1. Fibroadenoma
2. Breast cyst
3. Fat necrosis
4. Skin / SC lesions (Sebaceous cyst, Lipoma)

Other DDx of Benign breast lump
1. Galactocele (if lactating)
2. **Lipoma
3. **
Fat necrosis
4. Diabetic mastopathy
5. Infective causes: Mastitis, ***Breast abscess, Chronic recurrent subareolar infections e.g. from ductal ectasia
(6. Skin lesions: Sebaceous cysts
7. Postpartum engorgement)

Malignant (Irregular shape, Diffuse / Poorly defined border, Rapidly growing, Harder):
1. In-situ cancer
- DCIS
- LCIS
2. Invasive cancer
- Invasive Ductal
- Invasive Lobular
- Special types
3. Malignant phyllodes tumour (indeterminate)

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7
Q

***Histological types of Breast cancer

A

In-situ carcinoma:
1. **DCIS (Low / Intermediate / High grade)
(2. **
LCIS (Lobular carcinoma-in-situ): a premalignant condition / risk factor rather than cancer, commonly bilateral —> only surveillance needed)

Invasive carcinoma:
1. **Invasive Ductal (80%) (now called **Invasive carcinoma of no special type (NST))
2. **Invasive Lobular (3%)
3. **
Special types (unimportant, better prognosis)
- Tubular / Cribriform
- Papillary (Malignant form of Intraductal papilloma)
- Mucinous
- Medullary
- Paget’s (Nipple areolar complex involvement)
- Inflammatory (Skin infiltration)

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8
Q

***5 Steps in treating ANY cancer

A
  1. Confirm diagnosis (by biopsy / triple assessment)
  2. Metastatic workup (know extent of disease)
  3. Assessment of co-morbidities
  4. Nutritional assessment
  5. Definitive treatment
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9
Q

***Treatment options of Breast cancer

A

Curative treatment:
1. Surgery
- Mastectomy (Simple / Skin sparing / Nipple-Areolar sparing)
- Breast conserving surgery (BCS) (Wide local excision) (Need RT)

Adjuvant treatment (↓ recurrence risk + improve survival):
1. Chemotherapy
2. RT
3. Hormonal therapy
4. Targeted therapy

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10
Q

***Choice of treatment in Breast cancer

A

Patient factor:
1. Age / Menopause status

Tumour factor:
1. Tumour size
2. Tumour grade
3. No. of involved LN
4. ER / PR status
5. HER2 gene amplification (gene signatures)

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11
Q

***Surgical treatment option of Breast cancer

A

Aim:
- Oncological outcome vs Cosmetic outcome
1. Loco-regional control
2. Cosmesis

  1. Breast surgery
    - **Mastectomy
    - **
    BCS
  2. Axillary surgery
    - **Sentinel LN biopsy (SLNB) (+ Frozen section)
    - **
    Axillary dissection (AD)
  3. Reconstruction (additional option)
    - Autologous (Flap reconstruction)
    - Implant
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12
Q

CI to BCS

A

Absolute CI:
1. Tumor size **too large (Large Tumour to Breast size ratio)
- BCS will not result in a good cosmetic result
2. **
Multicentric cancer (across quadrants)
3. Where ***RT is contraindicated (e.g. Pregnancy, SLE, previous radiation, ipsilateral breast recurrence)

Relative CI:
1. Multifocal (within same quadrant)
2. Cancer underneath nipple or nipple involvement (can perform lumpectomy if large breasts)

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13
Q
  1. Mastectomy
A
  1. Simple mastectomy
    - removal of whole breast + some skin
    - most of the cases
  2. Skin sparing mastectomy
    - leave a lot more skin behind for future ***reconstruction
  3. Nipple / Areolar sparing mastectomy
    - reserved for selective low risk patients with **no nipple involvement of cancer
    - **
    prophylactic mastectomy
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14
Q
  1. Axillary surgery (SLNB / AD)
A

Landmark of LN: Pectoralis ***minor muscle (NOT major!!!)
- Level 1: Lateral
- Level 2: Posterior
- Level 3: Medial

Axillary dissection (AD):
- Clear ***Level 1 + 2 LN
- 20% lymphedema rate

NOT remove everything ∵ avoid lymphedema

Sentinel LN biopsy (SLNB):
- **First LN which drains the tumour
- **
Dye / Radioisotope (Dual tracer: injection of **methylene blue dye + **99Tc colloid in the sub-areolar area —> identify dyed or radioactive LN using gamma probe (“hot and blue”)
—> travel along lymphatics to Sentinel LN
—> biopsy for **frozen section (done **intra-operatively)
—> -ve: no need AD, +ve: need AD

Aim of SLNB:
- Suitable for **early stage cancers to avoid unnecessary AD
- Avoid **
complications related to AD
- Do less surgery without compromising **oncological outcome (e.g. early breast cancer often not involve LN)
- AD may not be necessary in patients with **
minimal tumor load in axillary LN + receiving BCS and RT

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15
Q

***Complications of AD

A

Early complication:
1. Nerve damage
- **Thoracodorsal bundle (i.e. artery + vein + nerve) —> **Latissimus dorsi —> Unable to raise trunk with upper limb e.g. climbing
- **Long thoracic nerve —> **Serratus anterior —> Pain, weakness, limitation of shoulder elevation, scapular winging
- **Intercostobrachial nerve —> **Sensory nerve to Triceps area
- Brachial plexus (uncommon ∵ more upward (area around level 3 LN))

  1. Vessel damage
    - **Thoracodorsal bundle
    - **
    Axillary vein

Late complication:
3. ***Lymphedema

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16
Q

***Surgical strategy for Breast cancer

A

4 combinations (2 Breast surgery + 2 Axillary surgery):
1. Mastectomy + SLNB
2. Mastectomy + AD (i.e. ***MRM: Modified radical mastectomy)
3. Breast conserving + SLNB
4. Breast conserving + AD

Choice of breast surgery (Mastectomy vs BCS?):
1. **Tumour response / size
2. **
Breast size
3. Tumour **location + **Multiplicity
4. Patient’s preference

(Modified Radical vs Radical mastectomy:
- Modified Radical: Mastectomy + Level 1+2 LN
- Radical: Remove pectoralis as well)

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17
Q
  1. Reconstruction
A

Types:
1. Implant based
- saline / silicon gel
- temporary / permanent
- one stage / two stage
- placed behind pectoralis muscle
- advantages: simpler procedure, **no donor site morbidity (i.e. no additional scar)
- disadvantages: **
↑ risk of infection, questionable ***durability, asymmetry more common

  1. Autologous tissue based
    - **Latissimus dorsi (LD)
    - **
    Transverse rectus abdominis myocutaneous (TRAM) —> Pedicle flap / Free flap / Deep inferior epigastric perforator flap (DIEP flap) (only skin + vessel, no muscle —> avoid herniation in future)
    - advantages: better cosmetic result
    - disadvantages: need ***additional scar / wound, may cause complications e.g. hernia in abdomen, ↑ chance of wound infection, longer surgery, more complex procedures
  2. Mixture of both types
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18
Q

Nipple-Areola reconstruction

A
  • Final touch up procedure (i.e. 2nd stage procedure)
  • Usually performed >=6 months after initial operation
  • Under local anaesthesia as day case
  • Use of ***local flaps to recreate nipple projection
  • Expect 50% reduction in height
  • Nipple sharing nearly obsolete
  • ***Tattoo to restore natural colour
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19
Q

Adjuvant therapy: RT

A

Indications:
1. >=4 LNs involved
2. Large tumours
3. Multifocal tumours
4. High grade
5. Lymphovascular permeation
6. ***BCS

Method:
- Whole breast RT / Partial breast RT / Intraop RT

Complications from radiation:
Early:
1. **Skin burn (preventable with radiogel)
2. **
Infection

Late:
3. **Lung fibrosis
4. **
Cardiomyopathy
5. **Lymphedema —> **Lymphangiosarcoma (Stewart-Treves syndrome) (Resection + RT / CT)
6. Skin discolouration
7. ***Sternal necrosis (in bilateral breast cancer)

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20
Q

Adjuvant therapy: Chemotherapy

A

Types:
1. Adjuvant: Kill of microscopic disease
2. Neoadjuvant: Pre-surgery control
3. Palliative / Salvage: At recurrence

Indications:
1. LN involvement
2. High risk (e.g. young age)
3. High grade
4. Large tumour

SE:
- N+V
- Injection site reaction, extravasation
- Hair loss
- **Bone marrow suppression (infection risk: Neutropenic fever)
- Allergic reaction
- Cardiotoxicity
- **
Neuropathy —> Numbness
- Nephrotoxicity
- Hepatotoxicity
- Amenorrhoea —> Infertility
- Hepatitis B flare up

21
Q

Adjuvant therapy: Hormonal therapy

A
  1. SERM (Selective estrogen receptor modulator) (e.g. Tamoxifen)
    - Suitable in **Pre + Postmenopausal patients
    - Increase **
    endometrial cancer risk, ***clotting disorders
    - Beneficial effect in blood lipids (lower LDL)
  2. Aromatase inhibitor (e.g. Letrozole)
    - Only in **Postmenopausal patients
    - Type I: Enzyme inactivator (steroidal)
    —> Exemestane
    - Type II: Competitive antagonist (non-steroidal)
    —> Anastrozole
    —> **
    Letrozole
    - **Decrease bone density
    - **
    Dyslipidaemia
    - ***Multiple joint pain
  3. Estrogen receptor antagonist (e.g. Fulvestrant)

Others:
4. Oophorectomy
5. Ovarian irradiation
6. Endocrine therapy (GnRH analogue) (Zoladex)

22
Q

Adjuvant therapy: Targeted therapy

A

Based on HER2 overexpression:
- Trastuzumab
- Pertuzumab
- Lapatinib

SE:
- Cardiotoxicity (Trastuzumab)
- Skin rash (Lapatinib)

Other new emerging drugs:
- CDK4/6 inhibitors
- Parp inhibitors
- Everolimus

23
Q

Neoadjuvant therapy

A
  1. Reduce size of tumour —> increase ***BCS rate
  2. Improve **local control + **long term outcome
24
Q

Benign breast disease

A
  • A spectrum of diseases
  • 90% of clinical presentation
  • ANDI (Aberrations of Normal Development and Involution of the breast) (—> now known as **Fibrocystic disease???)
    —> all encompassing term to describe a wide spectrum of benign breast diseases: **
    Cysts to ***Fibroadenoma
    —> allow better description of benign disease vs normal breast

S/S:
- Nodularity
- Tenderness
- Mobile

25
Q

***Fibrocystic disease: Physiological cyclical swelling + tenderness

A

**Fibrocystic disease (aka **Fibroadenosis)
- ***NOT a disease but general term that refers to a group of anomalies / symptoms
- main benign diagnosis in 30-40 yo

S/S:
1. **Cyclical mastalgia, **Lumpiness, **Nodularity
- areas of pronounced nodularity can mimic a lump
- **
premenstrual breast tenderness with mild swelling (engorgement of breast during menstrual period) —> result from variation in plasma concentration of gonadotrophic + ovarian hormones

  1. Breast can be nodular with ***no definitive mass —> Not considered abnormal breast
26
Q

***Fibroadenoma

A
  • A disease entity
  • most common benign breast tumour

Onset:
- any time after puberty
- most frequently 20-30 yo

S/S:
- **Painless (記住!)
- **
Well-circumscribed
- ***Freely movable tumours with rounded lobulated / discoid configuration —> “Breast mouse”
- Multiple in 10-15%
- Can become quite large

Prognosis:
- **NOT regress with time but tends to grow slowly
- Estimated incidence of malignancy: 0.12-0.3%
- **
Giant Fibroadenoma (>5 cm): may rapid growth
—> require excision (usually in young girls)
—> ∵ triple assessment not 100% accurate
—> have to rule out ***Phyllodes tumour

Treatment options:
1. Surveillance (USG)
2. Surgery (Excision)
3. HIFU
- can be used to treat various solid tumours (e.g. Fibroadenoma, Thyroid adenoma)

27
Q

Cyst

A
  • A disease entity
  • Commonest breast lump in 30-50 yo

Types:
1. **Simple cysts: Accumulation of fluid
2. **
Complex cysts: contain debris (solid components) —> need to rule out ***cystic tumour by Triple assessment

Treatment:
1. Aspiration to confirm nature (to rule out cystic tumour), also therapeutic to relieve symptom
2. **Fluid for cytology
3. **
Excision for suspicious lesions (e.g. complex cysts with solid components)

28
Q

Mastalgia

A
  1. ***Cyclical
  2. ***Non-cyclical
    - Muscular pain
    - Costochondritis
    - Non-specific
29
Q

Nipple discharge

A
  1. Unilateral vs Bilateral
    - ***Unilateral: pathological likely (involving single site)
    - Bilateral: physiological likely (e.g. lactation (but can be prolactinoma))
  2. Single ductal vs Multiductal
    - ***Single duct: pathological likely (involving single site)
    - Multiductal: physiological likely
  3. Nature of discharge
    - Milk (Galactorrhoea): Lactation, Prolactinoma
    - ***Blood / Brown (Suspicious): Intraduct papilloma, Malignancy
    - Yellowish / Green: Infection, Ductal ectasia
    - Serous / Colourless: Physiological, Ductal ectasia

Investigations:
Triple assessment
- +/- **Ductogram (inject contrast into diseased duct to look for filling defect —> identify cause of nipple discharge + location of lesion)
- +/- **
Ductoscopy (allow direct visualisation of lining of lactiferous ducts via a small fibreoptic scope)

30
Q

Other benign breast disease

A
  1. ***Sclerosing adenosis
  2. Radial scars and complex sclerosing lesions
  3. ***Papillomas
    - Intraductal papilloma (usually only involves single duct)
  4. **Atypical lesions
    - **
    Atypical ductal hyperplasia
    - Atypical lobular hyperplasia
    - Atypical columnar cell hyperplasia
    - etc.
    —> Atypia ↑ risk of breast cancer —> whenever see this in biopsy —> **excise (*surveillance NOT an option)
31
Q

Investigations: Imaging

A
  1. Mammography
    - used for screening
    - for older female
  2. USG
    - for younger female (denser breast: USG better penetration)
  3. MRI breast
32
Q
  1. Mammography
A

Malignant features on mammogram
1. **Clustered + **Pleomorphic microcalcifications
- apoptosis of dead cells (a normal phenomenon, but if ↑ cell turnover —> clustered instead of scattered)
- different size and shape (∵ some cells die quickly / slowly)
- Coarse calcifications: likely ***benign

  1. ***Spiculated border, High density mass
  2. Architectural distortion
    - ***tethering of skin
    - involvement of muscles etc.
  3. ***Asymmetrical density
    - compare both breasts + both views
33
Q
  1. USG
A

Benign features:
1. **Regular border
2. **
Oval in shape (grow along anatomical plane) (Width > Height)
3. Lobulated (sometimes)
4. **Posterior enhancement (indicate fluid in lesion) (Solid tumour: posterior shadowing)
5. **
Homogeneous

Malignant features:
1. **Irregular outline
2. **
Height > Width (i.e. grow across anatomical planes: invading up / down)
3. ***Posterior shadowing (Acoustic shadowing)
4. Echogenic halo

34
Q
  1. MRI breast
A

Not routinely done
- very sensitive but not specific

Indications:
1. Screening women at high risk of breast cancer (e.g. BRCA carriers)
2. Patients with **
breast implants / augmentation (obscure view on USG)
3. Evaluate questionable suspicious lesions seen on mammography / USG (
conflicting between imaging and histology)
4. Identify patients with clinical **
occult tumour presenting with positive axillary LN
5. Monitor result of neoadjuvant therapy
6. Identify extent of residual disease after excision which show positive margins

35
Q

Pathological exam (Biopsy)

A

Indication:
1. Evaluation of a palpable breast mass
2. Evaluation of a non-palpable breast mass
3. Evaluation of nipple discharge

4 techniques:
1. FNAC
2. Core biopsy
3. Incisional biopsy
4. Excisional biopsy

36
Q

FNAC vs Core biopsy

A

FNAC:
Advantages:
- safe, simple, inexpensive
- immediately distinguishes ***cysts from solid masses (tumour)

Disadvantages:
- cannot reliably distinguish **DCIS from invasive cancer
- cannot perform **
immunohistochemical staining

Core biopsy:
Advantages:
- distinguishes DCIS from invasive cancer
- allow **immunohistochemical staining for **ER / PR / C-erbB2 (HER2) status

Disadvantages:
- relatively ***more invasive, require local anaesthesia
- small stab incision

37
Q

Evaluation of a non-palpable breast mass

A
  1. Imaging
    - USG
    - Mammogram
    - MRI
  2. Biopsy (depends on which imaging picked up the lesion)
    - USG picked up —> USG guided FNAC / Core biopsy
    - Mammogram picked up —> Mammogram-guided biopsy (aka **Stereotactic guided biopsy —> for **microcalcifications)
    - MRI picked up —> MRI guided biopsy

Biopsy techniques:
1. FNAC / Core biopsy (when clinical suspicion)
2. Vacuum assisted core biopsy (***larger bore, more traumatic, vacuum to suck lesion, can achieve complete removal of small lesion)
3. Hookwire guided excisional biopsy (can do specimen mammogram / radiology / USG)
4. Radio-guided occult lesion localisation (ROLL)

Excisional vs Incisional biopsy:
Incisional:
- **Fungating / **Ulcerative tumour
- take out a strip of tissue directly from skin surface from **fungating edge (because **rapidly-growing area)
- cannot be done on a breast lump ***without ulceration

Excisional:
- when conflict between radiological vs core biopsy —> to be **100% sure
- cannot be done on a breast lump **
without ulceration

38
Q

Breast cancer screening

A
  • Aim to detect cancer as an asymptomatic + curable stage
  • Already proven decrease mortality rate in international studies
  • Problems: Psychological impact / over-diagnosis, Cost effectiveness

Why suitable for screening?
- Common disease / high prevalence
- Significant impact to population
- Detectable in early phase
- Low cost
- Accurate
- Specific
- Critical point before clinical diagnosis
- Short lag phase
- Tool is acceptable / tolerable to population
- Treatment available after diagnosis
- Treatment acceptable to population

“Standard” screening guidelines:
30s:
- ***Yearly breast examination
- Monthly self-breast examination

40s:
- Mammogram every ***2 years
- Yearly breast examination
- Monthly self-breast examination

50s:
- Mammogram every ***1 year
- Yearly breast examination
- Monthly self-breast examination

39
Q

Interactive tutorial: Management of breast cancer
Breast cancer screening

A

Pros:
- Decreased breast cancer mortality + total mortality
- Decreased morbidity from breast cancer (Reduction of late-stage breast cancer)

Cons:
- Radiation exposure
- False-positive and false-negative mammography results, additional imaging + biopsies
- Anxiety, distress, psychological responses

World:
- Variation in different countries depending on resources
- Voluntary: Not population screening
- Privately / Charity funded
- Means of screening: Mammography
- USG as part of screening (but lack evidence)
- Age 40: every 1-2 years
- Age 50: every 2 years
- Can consider screening earlier if family history

HK:
Past: Voluntary breast screening
Last year (2021):
***Risk based breast screening:
- Starting at age 44 based on risk calculation model
- Screening every 2 years

40
Q

Signs of Breast cancer on Mammogram

A
  1. **Microcalcifications
    - **
    Clustered / Segmental
    - **Pleomorphic (有大有細)
    - **
    Stellate patterns (星狀)
  2. ***Spiculated, high density mass
  3. ***Architectural distortion
  4. ***Asymmetrical density

**BiRADS score: Mammogram reporting (now for USG + MRI as well)
Category 0: Need further investigations (without any clinical examinations)
Category 1: Normal
Category 2: **
Benign
Category 3: Probably benign (<2% malignant)
Category 4: Suspicious of malignancy
Category 5: Highly suggestive of malignancy >=95%
Category 6: Malignancy proven with biopsy

41
Q

Limitations of mammography

A
  1. Breast implant
  2. Dense breast
  3. Paraffin calcification
42
Q

USG

A
  • Mammography still most sensitive test for breast cancer detection
  • USG used in conjunction with mammography
  • USG is commonly used in our locality to add diagnosis of breast lesion

Cons:
- USG not as sensitive for macrocalcification detection
- Less useful in fatty breast

Pros:
- Good at: mass lesions, cysts
- Easy to use, fast, cheap
- Useful in breasts with dense parenchyma

Reading USG:
- R93N: Right, 9 o’clock , 3 cm from nipple

43
Q

MRI breast indications

A
  • Screening women at ***high risk of breast cancer e.g. strong family history, hereditary cause
  • Evaluate ***questionable suspicious lesions seen on mammography / USG
  • Identify patients with **clinically occult (i.e. **non-palpable) tumour presenting with positive axillary nodes
  • Monitor result of ***neoadjuvant therapy
  • Exclude ***multifocal lesions when planning breast conservation surgery

MRI breast kinetic curve:
- leaky neovascularisation —> type 3 kinetic curve —> contrast concentration drops rapidly (vs benign disease will hold contrast)

44
Q

Staging of Breast cancer

A

Purpose (ALWAYS answer in exam):
1. Stage to plan treatment
2. Prognostication

Methods:
1. PET-CT / PET-MR

Alternative ways:
2. Bone scan
3. CT thorax / abdomen
4. USG

(AJCC TNM staging:
T stage:
T0: no evidence of primary tumour
Tis: Carcinoma in Situ
T1: Tumour **<2cm
- T1a: 0.1-0.5cm
- T1b: 0.5-1.0cm
- T1c: 1.0-2.0cm
T2: Tumour **
>2cm but <5cm
T3: Tumour **>5cm
**
T4: Tumour with **direct extension to
- T4a: chest wall (ribs, IC, serratus)

- T4b: skin (Peau d’orange, ulceration, satellite skin nodule)
- T4c: T4a + T4b
- T4d: inflammatory breast cancer

N stage (**Clinical / **Pathological):
N0: no lymph node involvement
N1: mets to movable ipsilateral level I, II axillary LN
N2: mets to ipsilateral level I,II axillary LN – clinically fixed or matted or mets to ipsilateral mammary LN in absence of axillary LN
N3: mets to ipsilateral infraclavicular (level III) lymph nodes, ipsilateral mammary LN, ipsilateral supraclavicular LN (with or w/o level I & II axillary LN)

M stage:
M0: no distant mets
M1: distant detectable metastasis (histologically proven > 0.2mm))

45
Q

Biopsy of Breast lumps

A
  1. FNAC
  2. Core biopsy (e.g. Vacuum assisted core biopsy)
  3. Excisional biopsy

If **palpable —> **Direct / Free hand
If **non-palpable —> **Image-guided
- USG guided
- Mammogram (Stereotactic) guided
- MRI guided
(others: Wire guided, Radio-guided occult lesion localisation (ROLL))

46
Q

Cytology Reporting Categories

A

C1: Inadequate
C2: Benign
C3: Atypia, probably benign
C4: Suspicious of malignancy
C5: Malignant

47
Q

***Risk factors of Breast cancer

A

Hormonal factors:
1. Early menarche <12
2. Late menopause >55
3. Pregnancy after age 30
4. Nulliparity
5. Use of OC pills / HRT
6. Obesity

Non-hormonal factors:
7. Family history of breast cancer (BRCA1, 2)
8. History of breast biopsy showing a premalignant condition, atypical ductal hyperplasia, proliferative fibrocystic changes, LCIS, DCIS
9. Smoking, Alcohol
10. Diet
11. Lack of exercise
12. Advanced age

48
Q

BRCA1, BRCA2

A

BRCA1:
- Breast cancer
- Ovarian cancer
- Prostate cancer
- Colon cancer

BRCA2:
- Breast cancer
- Male breast cancer
- Ovarian cancer
- Prostate cancer
- Laryngeal cancer
- Bile duct cancer
- Stomach cancer
- Colon (minimal) melanoma
- Pancreatic cancer

49
Q

Infertility issues

A

Pre-surgery / Pre-chemotherapy egg harvesting + storage can be offered