Breast Pathology Flashcards

1
Q

Breast Anatomy

A

15-20 lobes

Each composed of groups of lobules

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2
Q

What is the functional unit of the breast?

A

TDLU - terminal duct lobular unit

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3
Q

Triple Assessment

A

Clinical - history and examination
Radiological - mammography (>35y) USS
Pathological - FNA, core biopsy

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4
Q

Pathology reporting categories

A
C1/B1 - inadequate or not diagnostic
C2/B2 - benign
C3/B3 - favours benign
C4/B4 - favours malignant 
C5/B5 - malignant
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5
Q

Fibroadenoma

A

Commonest benign tumour
Typically under the age of 30
Firm, painless, mobile lump - may be multiple
Well circumscribed

Reassurance, dischange, excision

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6
Q

Fibrocystic change

A

result of minor aberrations in the normal response to cyclical hormonal changes
Typically in women 25-45 years
Changes affect the TDLU - characterised by fibrosis and cyst formation

Breast pain, tenderness, lumps/cysts

Triple assessment

Reassurance, analgesics, cyst aspiration, excision (rare)

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7
Q

Major risk factors for breast cancer

A

Increasing lifetime oestrogen exposure
Family history
Alcohol consumption

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8
Q

Clinical features of breast cancer

A
50% in outer quadrant of breast
Hard painless lump
fixed to wall or overlying skin
nipple incursion and skin dimpling
ulceration/fungation
peau d'orange
nipple eczema (Paget's disease)
palpable axillary nodes
metastatic disease
B symptoms
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9
Q

Breast cancer investigations

A

Triple assessment

Biopsy = grade
Staging needs to be done

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10
Q

Breast cancer pathophysiology

A

Most are invasive adenocarcinomas

75% are ductal carcinoma
10-15% are lobular carcinoma

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11
Q

Ductal Carcinoma In Situ (DCIS)

A

epithelial cells showing cytological changes of malignancy
present in the TDLE
basement membrane is in tact - cells have not invaded through

PRE CANCER

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12
Q

Invasive Ductal Carcinoma (IDC)

A

tumour cells have invaded through the basement membrane into adjacent tissue

CANCER

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13
Q

Paget’s disease of the nipple

A

due to the presence of DCIS cells in the epidermis which may extend along the major ducts and reach the nipple
the affected skin reacts to their presence and give the characteristic eczematous appearance

biopsy is required for a definite diagnosis

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14
Q

Invasion Lobular Carcinoma (ILC)

A

second most common type of invasive breast cancer
10-15% of cases
tumour cells infiltrating the normal breast tissues linear cords of cells (single file)
due to loss of E-cadherin-catenin cell adhesion system

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15
Q

What are the other less common types of breast cancer?

A

Tumular
Cribriform
Mucinous

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16
Q

What are the genetic subdivisions of invasive breast cancers?

A

Luminal A
Luminal B
HER-2-enriched
Basal-like

17
Q

Prognostic factors of breast cancer

A
Tumour stage (TNM)
Tumour grade
Histological subtype
Vascular invasion
Excision markings
Oestrogen receptor and HER2 status
18
Q

Oestrogen receptors (ER)

A

correlates with aggressiveness and predicts response to therapy

ER +ve = lower grade, less aggressive, likely to respond to hormonal therapy

ER -ve = higher grad,e more aggressive, less likely to respond to hormonal therapy

19
Q

HER2

A

oncogene that encodes transmembrane tyrosine kinase receptor
over expressed in about 15% of invasive breast cancers
over expression is associated with poorer prognosis, but good response to Herceptin

20
Q

What is the sentinel lymph node

A

the first node draining a cancer

if it doesn’t contain cancer then there is a very high likelihood that the cancer has not spread to any other nodes or elsewhere

21
Q

Advantages of the sentinel node technique

A

important prognostic information

patients with a negative sentinel node are spared an axillary node clearance

22
Q

how is the sentinel node identified?

A

dye/isotope injected into the tissue around the tumour
visually inspect nodes for staining and uses a gamma prove to assess which nodes have taken up the radionuclide
can then be identified and removed

23
Q

NHS breast screening programme

A

Identify premalignant or very early stage cancer

All women aged 50-70 (pushing to 47-73) are screened every 3 years

24
Q

Further assessment following screening

A

Imaging e.g. ultrasound
clinical examination
needle test, usually core biopsy