ERS33 Pathology Of Breast Cancer Flashcards

1
Q

Clinical presentations of breast cancer

A
  1. ***Presence of lump / thickening
  2. Change in size / shape
  3. ***Nipple retraction
  4. ***Blood nipple discharge

Unusual presentations (distinguish from benign lesion):

  1. ***Rash on nipple / surrounding area (Paget’s disease of breast)
  2. ***Dimpling of skin / skin appear inflamed (Inflammatory breast cancer)
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2
Q

What to feel for during breast exam

A

Best time to check: a few days ***after period (after Estrogen ↓ —> any potential fluid retention / cysts gone —> not obscure real lump)

  1. Lump (hard / immovable / lemon seed)
  2. LN (axilla, soft bean)
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3
Q

Paget’s disease of breast

A

***ALWAYS have underlying Intraductal / Invasive carcinoma

Clinical presentation:
Eczema, Rashes, ***Erosion of nipple + areola
—> Red, weeping
—> Dry, scaly, psoriatic (occasionally)

(may be mistaken with skin lesion)

Histology:
Invasion of epidermis by ***Paget’s cells (Carcinoma cells with Large, Round/oval nuclei, Pale cytoplasm, Mucin-containing)

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4
Q

Inflammatory breast cancer

A

Clinical presentation:
- **NO single lump / tumour
- Skin appear inflamed (may be ~ mastitis)
—> **
Red, Warm, Peau d’orange (Puckering of skin)
—> 1. Blockage of lymph vessel in the skin by cancer cells (Dermal lymphatic spread)
—> 2. Tumour cells infiltrate Fibrous septa + Suspensory ligament

Prognosis:

  • Poorer than typical invasive cancer
  • Higher chance of metastasis
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5
Q

Histological classification of breast carcinoma

A

Non-invasive:

  1. Ductal carcinoma-in-situ (DCIS)
  2. Lobular carcinoma-in-situ (LCIS)

Invasive:

  1. Invasive carcinoma of no special type (NST)
  2. Special subtypes
    - Invasive lobular carcinoma
    - Tubular carcinoma
    - Mucinous carcinoma
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6
Q
  1. Ductal carcinoma-in-situ (DCIS)
A
  • Confined within Ductal basement membrane
  • ***Micro-calcification —> may be detected by Mammography at early stage
  • 50% centrally situated —> form palpable mass

Histology:
- ***Cohesive cancer cells (癡埋一齊)

High grade comedo DCIS:

  • Large pleomorphic cells
  • ***Central comedo necrosis (necrosis of ducts)
  • 50% evolve into invasive carcinoma within 5 years

Low grade non-comedo DCIS:
- only 30% evolve into invasive carcinoma within 10-15 years

—> subsequent invasive carcinoma usually in ***same area as initial DCIS (invade into surrounding CT stroma)

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7
Q
  1. Lobular carcinoma-in-situ (LCIS)
A
  • Cancer cells within Acini
  • Confined within Acini basement membrane
  • Peri-menopausal women, less common with advancing age
  • ***NO distinguishing clinical features —> usually radiologically undetectable / impalpable —> may be missed by Mammography

Gross:

  • Multicentric (70%) (i.e. multiple areas of breast)
  • Bilateral (20-35%)
  • Concentrated within 5cm of nipple in outer / upper inner quadrants

Histology:

  • Lobules expanded by cancer cells
  • Smaller, ***Discohesive cancer cells (散開)

Prognosis:

  • 10x greater chance of developing into invasive carcinoma than general population
  • absolute risk 20-25% in 15 years

—> Site of later invasive carcinoma equally divided between **either breast
—> **
may be Ductal / Lobular

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8
Q
  1. Invasive carcinoma of no special type (NST)
A

Aka:

  • Ductal carcinoma (NST)
  • Invasive carcinoma (NOS)
  • Infiltrating ductal carcinoma
  • **MOST common type of breast cancer
  • a heterogeneous group of tumours
  • fail to exhibit sufficient characteristics to be classified as a specific histological type
  • 70% of invasive breast cancer

Gross:

  • ***Poorly defined
  • Hard, yellow-grey mass
  • ***Radiating fibrous trabeculae (Fibrosis)
  • ***Gritty sensation and chalky streaks (crab-like, legs of crabs infiltrating)

Histology:

  • Clusters of carcinoma cells (poorly differentiated / more differentiated)
  • Nuclear pleomorphism
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9
Q
  1. Special subtypes of invasive carcinoma
A
  1. Invasive lobular carcinoma
    - 5% of all breast tumours
    - Multifocal + Bilateral
    - Poorly circumscribed mass
    - Single cell infiltration
    - Single file (Indian filing: 一列隊) / Concentric rings around a duct (Target-like lesion) of ***Small-medium tumour cells (∴ lesion may be impalpable)
  2. Tubular carcinoma
    - 90% of tumour composed by **Open tubules lined by **Single layer of cells
    - Excellent prognosis
    - Distant metastasis unlikely, rarely kill
  3. Mucinous carcinoma
    - Older women
    - Slow-growing circumscribed mass
    - produce Bulky, **soft, gelatinous material
    - **
    Islands of tumour cells floating in ***large lakes of mucin
    - Excellent prognosis
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10
Q

Spread of breast carcinoma

A
  1. Lymphatic spread
    - influenced by location
    - Lateral tumours (more common): **Axillary LN (level 1-3 —> Supraclavicular LN)
    - Medial / Deep tumours: **
    Internal mammary LN

Sentinel LN
- 1st LN most likely to spread to
- Sentinel LN biopsy
—> determine whether cancer cells are present
—> -ve result suggest cancer not yet spread to nearly LN / other organs
—> patient spared from further LN surgery
—> ↓ potential SE of LN surgery e.g. lymphoedema (e.g. swelling of arm)

  1. Haematogenous spread
    - Bone (more common), Lung, Liver, Ovaries, Adrenal glands, Brain
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11
Q

Prognosis of breast cancer

A

Different types of breast cancer —> Differ
Prediction based on statistical probability generated from outcomes of large series of patients

Options of treatment:

  1. ***Local excision
  2. Partial mastectomy / ***Mastectomy
  3. Combinations of **Radiotherapy + **Chemotherapy
    - Hormonal therapy SERMs e.g. Tamoxifen
    - Targeted therapy e.g. Herceptin

Clinical-pathological prognostic assessment:

  • Appropriate clinical decision making
  • Predict survival in >= first 5 years

Importance of Pathology report / Pathologist:

  • Diagnosis of breast cancer
  • Prognostic + Predictive profile of each patient
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12
Q

Pathology examination for stereotactic image guided excision for impalpable lesion

A
  • **Block selection (一階一階) to establish character lesion and size
  • superior / inferior / lateral / medial
  • need to correlate with specimen X-ray
  • embedded blocks in numbered sequence —> allow reconstruction and size assessment
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13
Q

Prognostic / Predictive marker

A
  1. Size
  2. Histological type / grade
    - Grade I - III (based on Tubule formation (more the better), Nuclear grade, Mitotic rate)
  3. Presence of DCIS
    - assessment of margins, size of lesion, classification of pathological subtype
    - low / intermediate / high nuclear grade (comedo necrosis)
  4. Lympho-vascular invasion
    - predictor of local recurrence after conservation therapy
  5. LN status (Number + Level of nodal involvement)
  6. Proliferation rate
  7. Clearance from resection margins
  8. Steroid hormone receptor status (nuclear receptor)
    - ER +ve tumour are responsive to ***Anti-estrogen treatment
  9. HER2 oncogene overexpression (membrane receptor)
    - marker of poor prognosis in LN +ve patients
    - predict response to chemotherapy
    —> **Doxorubicin-based
    —> **
    Herceptin (Anti-HER2 Ab)
    - Immunohistochemical assay widely used but reliability being questioned
    —> ***Fluorescent in-situ hybridisation (FISH) gold standard to see whether gene is amplified
    —> but expensive + time-consuming
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14
Q

HER-2 breast cancer

A

HER-2 +ve:

  • more aggressive than other types of breast cancer
  • less responsive to hormone treatment
  • treatments specifically target HER2 are very effective:
    1. Trastuzumab (Herceptin)
    2. Lapatinib (Tykerb) (Tyrosine kinase inhibitor)
    3. Doxorubicin (Adriamycin)
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15
Q

Stages of breast cancer

A

Determining staging by:

  1. Pathology - Sentinel LN / LN biopsy
  2. Imaging - CXR, Bone scan, CT, PET

Revised TNM staging by AJCC:

  1. pTis - DCIS (including Paget’s disease)
  2. pT1
    - pT1a (<= 5mm)
    - pT1b (5-10mm)
    - pT1c (10-20mm)
  3. pT2 - 20-50mm
  4. pT3 - > 50mm
  5. pT4 - direct extension to skin / chest wall
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16
Q

Molecular classification of breast cancer

A

New way of tumour classification

∵ Different tumour subtypes —> Distinct gene expression signatures

Gene expression profiling by ***cDNA microarray
—> prediction for individual patients by molecular testing
—> High concordance in outcome predictions
—> but showed absence of gene overlap
—> each molecular platform with its pros / cons

Tumour classification now done according to

  1. Clinical outcome (prognostic)
  2. Response to therapy (predictive)

***Major molecular subtypes:
1. Luminal (ER +ve)
2. HER2 (HER +ve, ER -ve)
3. Basal-like (HER -ve, ER -ve, High basal epithelial/CK)
—> each with characteristically different clinical features, treatment response, outcome
—> broadly divided into ER +ve / -ve
—> can also be approximated with use of traditional immunomarkers ER, PR, HER2 (thus no need for gene profiling)

17
Q

Luminal vs HER2 vs Basal-like

A

ER +ve:

  1. Luminal:
    - ER/PR +ve
    - **Hormone responsive
    - **
    Good prognosis
    - Luminal A (ER/PR +ve, HER2 -ve), Luminal B (triple +ve)

ER -ve (HER2 / Basal-like):

  • Hormone non-responsive (can only give chemo)
  • Poor prognosis
  1. HER2:
    - ER/PR -ve
    - **Herceptin / Anthracyclines-based responsive
    - **
    Poor prognosis
  2. Basal-like:
    - ER/PR/HER2 -ve
    - No response to endocrine treatment / Herceptin
    - only sensitive to **Platinum, **PARP inhibitors
    - ***Poor prognosis