Gynae cancers Flashcards

1
Q

When to do hysteroscopy and biopsy?

A

If 4mm or more (endometrial thickness) –> do hysteroscopy and endometrial biopsy

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2
Q

Types of cervical cancer?

A

squamous cell cancer (80%)

adenocarcinoma (20%)

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3
Q

Features of cervical cancer?

A

may be detected during routine cervical cancer screening
abnormal vaginal bleeding: postcoital, intermenstrual or postmenopausal bleeding
vaginal discharge

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4
Q

RFs for cervical cancer?

A

Human papillomavirus (HPV), particularly serotypes 16,18 & 33 is by far the most important factor in the development of cervical cancer. Other risk factors include:
smoking
human immunodeficiency virus
early first intercourse, many sexual partners
high parity
lower socioeconomic status
combined oral contraceptive pill*

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5
Q

Mechanism that HPV causes cervical cancer?

A

HPV 16 & 18 produces the oncogenes E6 and E7 genes respectively
E6 inhibits the p53 tumour suppressor gene
E7 inhibits RB suppressor gene

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6
Q

regularity of cervical screening?

A

25-49 years: 3-yearly screening
50-64 years: 5-yearly screening

cervical screening cannot be offered to women over 64

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7
Q

What happens to cervical screening in pregnancy?

A

cervical screening in pregnancy is usually delayed until 3 months post-partum unless missed screening or previous abnormal smears.

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8
Q

Explain how cervical smears are tested?

A

sample is tested for high-risk strains of human papillomavirus (hrHPV) first and cytological examination is only performed if this is positive.

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9
Q

Mx of negative hrHPV?

A

return to normal recall, unless
the test of cure (TOC) pathway: individuals who have been treated for CIN1, CIN2, or CIN3 should be invited 6 months after treatment for a test of cure repeat cervical sample in the community
the untreated CIN1 pathway
follow-up for incompletely excised cervical glandular intraepithelial neoplasia (CGIN) / stratified mucin producing intraepithelial lesion (SMILE) or cervical cancer
follow-up for borderline changes in endocervical cells

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10
Q

Mx of positive hrHPV?

A

samples are examined cytologically

if the cytology is abnormal → colposcopy
this includes the following results:
this includes the following results:
borderline changes in squamous or endocervical cells.
low-grade dyskaryosis.
high-grade dyskaryosis (moderate).
high-grade dyskaryosis (severe).
invasive squamous cell carcinoma.
glandular neoplasia

if the cytology is normal (i.e. hrHPV +ve but cytologically normal) the test is repeated at 12 months:

  • if the repeat test is now hrHPV -ve → return to normal recall
  • if the repeat test is still hrHPV +ve and cytology still normal → further repeat test 12 months later:
    • If hrHPV -ve at 24 months → return to normal recall
    • if hrHPV +ve at 24 months → colposcopy
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11
Q

Mx of inadequate cervical screen sample?

A

If the sample is ‘inadequate’
repeat the sample within 3 months
if two consecutive inadequate samples then → colposcopy

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12
Q

Mx of individuals who have been treated for CIN?

A

should be invited 6 months after treatment for a test of cure repeat cervical sample in the community.

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13
Q

WHen should a woman >65yo be screened for cervical cancer?

A

A recent cervical cytology sample is abnormal.

They have not had a cervical screening test since 50 years of age and they request one.

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14
Q

WHen should a cervical sample not be taken?

A

if the woman:
Is menstruating.
Is less than 12 weeks postnatal.
Is less 12 weeks after a termination of pregnancy, or miscarriage.
Has a vaginal discharge or pelvic infection — treat the infection and take the sample on another occasion.

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15
Q

Situations where more frequent cervical screening required?

A

kidney failure and require dialysis - screen at siagnosis

about to undergo organ transplantation - screen within a year before transplantation

are starting sytotoxic drugs for rheum disorders - if the screening history is incomplete at the start of treatment.

HIV positive - at Dx and annually therafter

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16
Q

Define CIN 1, 2, and 3

A

CIN1 — one-third of the thickness of the surface layer of the cervix is affected.
CIN2 — two-thirds of the thickness of the surface layer of the cervix is affected.
CIN3 — sometimes called high-grade or severe dysplasia or stage 0 cervical carcinoma in situ. The full thickness of the surface layer is affected.

17
Q

Appearance of CIN on colposcopy?

A

ceto-white epithelium (AWE).
• V ascular abnormalities, especially mosaic and punctuation.
• B izarre or grossly abnormal vessels are suggestive of micro-invasive
carcinoma.

18
Q

Mx of CIN 1, and 2,3

A

CIN 1:
C onservative monitoring with colposcopy and/or cytology every
6mths.
• LLETZ if persistent.

CIN2,3:
LLETZ
- follow-up cytology and high risk HPV test-of-cure at 6mths.

19
Q

Complications of LLETZ?

A
Short term
• Haemorrhage.
• Infection.
• Vaso-vagal reaction.
• Anxiety (disproportionately high in colposcopy clinic attenders).

Long term
• Cervical stenosis (dysmenorrhoea and/or diffi culty in follow-up).
• Cervical incompetence and premature delivery (evidence suggests
absolute risk of adverse effect on neonatal outcome is very low).

20
Q

RFs for endometrial cancer?

A
obesity
nulliparity
early menarche
late menopause
unopposed oestrogen. The addition of a progestogen to oestrogen reduces this risk (e.g. In HRT). The BNF states that the additional risk is eliminated if a progestogen is given continuously
diabetes mellitus
tamoxifen
polycystic ovarian syndrome
hereditary non-polyposis colorectal carcinoma
21
Q

Ix for endometrial cancer?

A

first-line investigation is trans-vaginal ultrasound - a normal endometrial thickness (< 4 mm) has a high negative predictive value
hysteroscopy with endometrial biopsy

22
Q

protective factors for endometrial cancer?

A

COCP and smoking

23
Q

Mx of endometrial hyperplasia?

A

simple endometrial hyperplasia without atypia: high dose progestogens with repeat sampling in 3-4 months. The levonorgestrel intra-uterine system may be used
atypia: hysterectomy is usually advised

24
Q

Simple vs complex endometrial hyperplasia?

A

depends on the

glandular:stromal ratio (much less stroma in complex hyperplasia).

25
Q

Histology of endometrial carcinoma?

A

Back-to-back atypical glandular

cells (i.e. no stromal component) = endometrial carcinoma.

26
Q

Causes of unopposed oestrogen?

A

E ndogenous:
• p eripheral conversion in adipose tissue of androstenedione to
oestrone
• o estrogen-producing tumour (granulosa cell tumour)
• p olycystic ovarian syndrome or anovulatory cycles at menarche or
during climacteric period (lack of progesterone as no luteal phase).

Exogenous:
• o estrogen-only HRT
• t amoxifen (oestrogen agonist in endometrial tissue).

27
Q

When to perform an endometrial biopsy?

A

Perform endometrial sampling if ET ≥ 4mm or persistent bleeding in woman with ET <4mm (in which case consider formal hysteroscopy).

28
Q

RFs for ovarian cancer?

A

BRCA1 and 2, lynch syndrome
increasing age
nulliparity
family history

29
Q

What cancers is lynch syndrome associated with?

A

Also known as Hereditary Non Polyposis Colorectal Cancer

• Associated with colorectal, ovarian and endometrial cancer

30
Q

protective factors for ovarian cancer?

A

multiparity, COCP

31
Q

Px of ovarian cancer?

A
Asymptomatic
•
Non specific GI symptoms: bloating,
NV, change in bowel habit, early satiety
•
Chronic pelvic pain
•
Incidental finding
32
Q

What is a red flag for ovarian Ca?

A

A new diagnosis of IBS

over the age if 50 is a red flag

33
Q

Ix for ovarian cancer?

A

First Step: CA
125 and Transvaginal Ultrasound Scan (TVUS)

then RMI (RMI > 200 =
>75% Risk of Ovarian Cancer)

if greater than 200 –>Gynae MDT 2ww for CT abdo pelvis

34
Q

How to identify type of ovarian cancer?

A

Exploratory laparoscopy - offers dx and provides tx

Peritoneal washings
-
Peritoneal biopsies
-
TAH and BSO
-
Lymph node dissection
-
Omentectomy
35
Q

Tumour markers for suspected ovarian cancer?

A

CA125 in all women

if less than 40yo - measure levels of AFP and beta-hCG as well as serum CA125, to identify women who may not have epithelial ovarian cancer.

36
Q

When might CA125, Carcinoembryonic antigen (CEA) and CA19.9 be raised?

A

CA125 - raised in 80% of epithelial cancers
CEA - raised in colorectal cancers
CA19.9 0 raised in mucinous tumours (more likely to have normal CA125). Also pancreatic and breast