Session 7: Breast Cancer Flashcards

1
Q

Physiological changes seen in breast tissue.

A

Prepubertal breast with a few lobules.

Menarche hits and there is an increase in lobules, increased volume of interlobular stroma.

During menstrual cycle after ovulation there is proliferation and stromal oedema. With menstruation there is a decrease in size of lobules.

In pregnancy there is an increase in size and number of lobules, there is a decrease in stroma, and there are secretory changes.

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2
Q

Physiological changes in increasing age of breast tissue.

A

Terminal duct lobular units decrease in number and size.

The interlobular stroma is replaced by adipose tissue.

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3
Q

How may breast conditions present?

A

Pain

Palpable mass

Nipple discharge

Skin changes

Lumpiness

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4
Q

Give examples of types of pain experience in breast conditions.

A

Cyclical or diffuse (most commonly physiological)

Non-cyclical and focal (might be a ruptured cyst, injury or inflammation)

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5
Q

Give examples of breast conditions that cause a palpable mass.

A

Normal nodularity

Invasive carcinomas

Fibroadenomas

Cysts

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6
Q

When are palpable breast mass most worrying?

A

When they are hard, craggy and fixed

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7
Q

What are the most worrying findings on mammographs?

A

Densities

Calcifications

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8
Q

What might densities suggest?

A

Invasive carcinomas

Fibroadenomas

Cysts

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9
Q

What might calcifications suggest?

A

Ductal carcinoma in situ (DCIS)

Benign changes

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10
Q

Women of which ages are invited to mammographic screening each year?

A

47-73 years of age

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11
Q

Most common benign breast tumour

A

Fibroadenoma

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12
Q

What kind of tumour is most common in <30 years?

A

Fibroadenomas

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13
Q

When are phyllodes tumours most present?

A

In 60s

They can be malignant

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14
Q

In which ages are breast cancer common?

A

Rare in young ages and especially younger than 25.

Incidence rises with age and 77% of all breast cancers occur in women >50 years

The average age of diagnosis is 64 years.

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15
Q

Explain acute mastitis.

A

Almost always occurs during lactation and is usually due to S. aureus infection from nipple crack and fissures.

The presentation is usually erythematous and painful, Patient is also pyrexic.

It may produce breast abscesses.

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16
Q

How is acute mastitis treated?

A

Expressing milk and antibiotics

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17
Q

What is fat necrosis in breast tissue?

A

An inflammatory condition which presents as a mass, skin changes or mammographic abnormality.

There is often a history of trauma or surgery.

It can mimic carcinoma both clinically and mammographically.

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18
Q

Explain fibrocystic change.

A

Benign epithelial lesions which are the most common breast lesions.

They may present as a mass or mammographic abnormality.

The mass often disappears after fine needle aspiration.

Can mimic carcinoma clinically and mammographically.

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19
Q

Histology of fibrocystic change.

A

Cyst formation

Fibrosis

Apocrine metaplasia

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20
Q

Give examples of stromal tumours.

A

Fibroadenoma

Phyllodes tumours

Lipoma

Leiomyoma

Hamartoma

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21
Q

Macroscopical features of fibroadenomas.

A

Present with a mass, usually mobile or mammographic abnormality.

Often called breast mouse as they are mobile and elusive.

Can be multiple and bilateral.

They might grow very large and replace most of the breast tissue.

They are well circumscribed, rubbery and greyish/white.

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22
Q

What is gynaecomastia?

A

Enlargement of male breast which can be either unilateral or bilateral.

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23
Q

What is gynaecomastia caused by?

A

Relative decrease in androgen effect or increase in oestrogen effect.

Can often be seen at pubery and in the elderly.

It can mimic breast cancer especially if it is unilateral.

However there is no increased risk of cancer.

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24
Q

Give examples of conditions causing gynaecomastia.

A

Neonatal secondary to circulating maternal and placental oestrogens and progesterone.

Transient gynaecomastia in puberty as oestrogen production peaks earlier than testosterone.

Klinefelter’s syndrome (XXY)

Oestrogen excesses like due to liver cirrhosis

Gonadotrophin excess (functioning testicular tumour, leydig and sertoli cell tumours, testicular germ cell tumours)

Drug-related

25
Q

Give examples of drug-related gynaecomastia.

A

Spironlactone

Chlorpromazine

Digitalis

Cimetidine

Alcohol

Marijuana

Heroin

Anabolic steroids

26
Q

Most common type of breast cancer.

A

95% are adenocarcinomas

27
Q

Where are most breast cancer seen?

A

In the upper outer quadrant

28
Q

Give examples of risk factors of breast cancer

A

Gender

Uninterrupted menses

Early menarche

Late menopause

Reproductive history such as parity and age at first full term pregnancy

Obesity and high fat diet

Exogenous oestrogens

Geographic influence

Previous breast cancer

Radiation

Breast density

29
Q

How common is hereditary breast cancer

A

10% of breast cancers

30
Q

What genes are associated with breast cancer?

A

BRCA1

BRCA2

p53 (Li-Fraumeni syndrome)

31
Q

What are BRCA 1 and BRCA 2.

A

Tumour suppressor genes which increases the risk of breast cancer significantly.

The lifetime risk of female carriers is 60% to 85%

32
Q

How can breast carcinoma be classified?

A

Divided into in situ and invasive

Divided into ductal or lobular

33
Q

What is an in situ breast carcinoma?

A

Neoplastic population of cells that is limited to duct and lobular by the basement membrane

The myoepithelial cells are preserved

They do not invade into vessels and therefore cannot metastasise or kill the patient.

34
Q

If a ductal carcinoma in situ cannot metastasise or kill the patient, why is it a problem then?

A

Because it is a precursor of invasive carcinoma.

It can still spread through ducts and lobular and be extensive.

35
Q

What is Paget’s disease?

A

Cells that can extend to nipple skin without crossing the basement membrane.

They are unilateral red and crusting nipple.

36
Q

How does invasive carcinoma differ from DCIS?

A

Invasive means it has invaded beyond the basement membrane and into the stroma.

It can invade into vessels and can therefore also metastasise to lymph nodes and other sites.

By the time a cancer is palpable more than half of the patients will have axillary lymphnode metastasis.

37
Q

What is peau d’orange?

A

Involvement of lymphatic drainage of skin in breast cancer.

38
Q

You can see breast cancer sometimes with the naked eye.

How?

A

In breast cancer there can be nipple retraction.

39
Q

How is invasive breast carcinoma classified?

A

Invasive ductal carcinoma, no special type (IDC NST)

Invasive lobular carcinoma

Other types such as tubular and mucinous.

40
Q

Most common invasive breast carcinoma

A

Invasive ductal carcinoma (70-80%)

Invasive lobular carcinoma (5-15%)

Mucinous (1-6%)

Tubular (1-2%)

41
Q

Explain the features of invasive ductal carcinoma

A

Well differentiated with tubules lined by atypical cells.

There is also a poorly differentiated type with sheets of pleomorphic cells.

42
Q

Prognosis of IDC NST

A

35-50% 10 year survival

43
Q

Explain features of invasive lobular carcinoma

A

Infiltrating cells in a single file and cells that lack cohesion.

Similar prognosis to IDC NST

44
Q

How does breast cancer spread?

A

Lymph nodes via lymphatics and then usually to the ipsilateral axilla.

Distant metastases via blood vessels and then to bones, lungs, liver and/or brain.

45
Q

There are some odd targets of invasive lobular carcinoma.

Give examples.

A

Peritoneum

Retroperitoneum

Leptomeninges

GI tract

Ovaries

Uterus

46
Q

What factors determine prognosis in breast cancer?

A

Whether it is in situ or invasive

Tumour stage (TNM)

Tumour grade

Histological subtype

Molecular classification and gene expression profile

47
Q

What is the molecular classification of breast cancer?

A

Breast carcinoma can either be oestrogen receptor positive or oestrogen receptor negative.

If it is positive then you look at Her2 positive or negative.

If it is negative then you also look at Her2 positive or negative

There is a better prognosis of oestrogen receptor positive breast carcinoma.

48
Q

How is breast cancer investigated and diagnosed?

A

Triple approach of:

Clinical - history, FH and examination

Radiographic imaging - mammogram and ultrasound scan

Pathology with a core biopsy and fine needle aspiration cytology

49
Q

What do you look for on mammographic screening?

A

Asymmetric densities, parenchymal deformities and calcifications.

50
Q

What are the therapeutic approaches in breast cancer?

A

Breast surgery

Axillary surgery

Post-operative radiotherapy to chest and axilla

51
Q

When is breast surgery done?

A

Mastectomy or breast conserving surgery where the decision depends on the patient choice

It also depends on the size and site of tumour and number of tumours as well as size of breast.

52
Q

When is axillary surgery done?

A

The extent depends on whether there are involved nodes (sentinel node sampling or axillary dissection)

53
Q

What is sentinel lymph node biopsy?

A

Reduces the risk of postoperative morbidity and is an intraoperative lymphatic mapping with dye and/or radioactivity of the draining of sentinel lymph node(s).

Sentinel lymph node is the most likely to contain breast cancer metastases.

54
Q

When is axillary dissection avoided?

A

If the sentinel lymph nodes are negative.

55
Q

Give examples of systemic treatment of breast cancer.

A

Chemotherapy

Hormonal treatment

Herceptin treatment

56
Q

What is hormonal breast cancer treatment?

A

E.g. tamoxifen which is given in oestrogen receptor positive breast cancers. (ER+)

Doesn’t work effectively in ER-

57
Q

Explain herceptin treatment.

A

Depends on the Her2 receptor status.

If the cancer is Her2 receptor positive then Herceptin treatment can ensue.

Herceptin is trastuzumab which is a humanised monoclonal antibody against the Her2 protein.

58
Q

How do we improve survival from breast cancer?

A

Early detection

Neoadjuvant chemo

Use of new therapies such as herceptin

Gene expression profiles

Genetic screening

59
Q
A