Neoplasms of the Reproductive System Flashcards

1
Q

State the type of cancer found in vulva

A

Squamous cell carcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Describe the epidemiology of vulva tumours

A
  • More commonly found in older women

- 30% of cancers are related to HPV infections

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Describe the possible causes of tumours of the vulva

A
  • Vulvar intraepithelial neoplasia (VIN)
    • Atypical squamous cells within the epidermis - no invasion
    • Precursor for vulval squamous cell carcinoma
  • Vulval squamous cell carcinoma
    • Involve invasion of the epidermis
    • Spreads initially to inguinal, pelvic, iliac and para-aortic lymph nodes
    • Can also spread to lungs and liver
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Describe the epithelium at the cervix

A
  • Endocervix covered by glandular epithelium
  • Exocervix coveted by squamous cell epithelium
  • Transformation zone is area between glandular and squamous cell epithelium and where cell proliferation takes place
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Describe how HPV can cause cervical cancer

A
  • Infect immature metaplastic squamous cells in transformation zone
  • Produce viral proteins E6 and E7
    • E6 inhibits p53 and E7 inhibits RB
    • Causes inability to repair damaged DNA and increased proliferation of cells
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

List the risk factors of cervical cancer

A
  • Sexual intercourse
  • Early first marriage
  • Early first pregnancy
  • Multiple births
  • Many partners
  • Partner with carcinoma of the penis
  • Long term use of oral contraceptive pills
  • Immunosuppression - susceptible to HPV infections
  • Smoking
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

State the pathology related to cervical tumours

A
  • Cervical intraepithelial neoplasia (CIN)

- Invasive cervical carcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Describe cervical intraepithelial neoplasia and its treatment

A
  • Dysplasia of squamous cells within the cervical epithelium, induced by infection with high risk HPV
  • A small proportion of CIN I progress to CIN II and then CIN III
    • CIN III is a carcinoma in situ - with 10% progressing to invasive carcinoma
  • Treatment - progression of CIN identified through cryoscopy and treatment based on progression
    • CIN I treated through follow-up or cryotherapy
    • CIN II and CIN III treated by superficial excision - large loop excision of the transformation zone
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Describe invasive cervical carcinoma presentation and treatment

A
  • 80% squamous cell carcinoma and 15% adenocarcinoma
  • May be exophytic (localise on surfaces) or infiltrative
  • Spreads to para-cervical soft tissue, bladder, ureters, rectum and vagina
    • Spread to lymph nodes and can spread distally
  • Present with post-coital, intermenstrual or postmenopausal vaginal bleeding
  • Treatment - micro-invasive carcinomas treated with cervical cone excision
    • Invasive carcinomas require hysterectomy, lymph node dissection and chemotherapy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Explain the principles of HPV vaccination

A
  • Given to girls 12-13 and protects for 10 years (period highest risk to infection)
  • Doesn’t protect against all high risk infections - screening still needed
  • Currently boys not vaccinated, but vaccination can protect against penile cancer and decrease risk of spread
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Explain the principles of cervical screening

A
  • Cervix accessible to visual examination (colposcopy) and sampling
  • Slow progression from precursor lesions to invasive cancers - have time to screen and detect
    • Early detection and treatment
  • Cells from the transformation zone are scraped off and stained (smear test)
  • Can also test for HPV DNA in cervical cells
  • Starts age 25, then every 3 years until 50, when it becomes every 5 years
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Explain endometrial hyperplasia link to endometrial adenocarcinoma

A
  • Endometrial hyperplasia common precursor to endometrial carcinoma
  • Increased gland to stroma ratio
  • Associated with prolonged oestrogen stimulation (causes proliferation of endometrium)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Explain endometrial adenocarcinoma epidemiology and presentation

A
  • Most common invasive cancer of the female genital tract
  • Common in older women
  • Present with irregular or postmenopausal vaginal bleeding - early detection and good survival rate
  • Can be polypoid or infiltrative
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Describe the 2 types of endometrial adenocarcinomas

A
  • Endometrioid
    • More common
    • Mimics proliferative glands - many glands seen microscopically
    • Arises after endometrial hyperplasia
    • Associated with unopposed oestrogen and obesity (increased adipose tissue and therefore oestrogen)
    • Spreads by myometrial invasion and direct extension to adjacent structures, to local lymph nodes and distant sites
  • Serous carcinoma
    • Poorly differentiated, aggressive worse prognosis
    • Can spread very easily - to Fallopian tubes, peritoneal surfaces
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Describe the presentation and prognosis of leiomyoma

A
  • Leiomyoma (fibroids) - most common tumour in women
  • Benign tumour of myometrium (uterine smooth muscle)
  • May be asymptomatic but can cause heavy periods, urinary frequency, infertility
  • Very rarely becomes malignant
  • Growth is oestrogen dependent and usually regress after menopause
  • Well circumscribed, round, firm and white tumours
  • Bundles of smooth muscle - resembles normal myometrium
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Describe a cancerous tumour of the myometrium

A
  • Uterine leiomyosarcoma
  • Highly malignant
  • Doesn’t arise from leiomyomas
  • Commonly metastasize to the lung
17
Q

Describe the epidemiology of ovarian tumours

A
  • Most are benign and occur in younger women
  • Malignant tumours occur in older women
  • Tend to spread beyond ovaries before time of presentation so poor prognosis
  • Commonly bilateral
  • Some associated with BRCA mutations - possible breast cancer or family history of breast cancer
18
Q

Describe the presentation of ovarian tumours

A
  • Most non-functional - do not produce hormones
    • Produce symptoms when they become large, invade adjacent structures or metastasize
    • Abdominal pain, abdominal distension, ascites
  • Can be functional - produce hormones (high oestrogen in blood)
    • Menstrual disturbances, inappropriate sex hormones
19
Q

Describe the spread of ovarian cancer and how its monitored

A
  • Commonly spread to other ovary and through peritoneal cavity
  • Spread to regional nodes as well as liver and lungs
  • Serum CA-125 used in diagnosis and to monitor disease recurrence and progression
20
Q

State the classification of ovarian cancer

A
  • Epithelium tumours (Mullerian)
  • Germ cell ovarian tumours
  • Sex cord-stromal tumours
  • Metastases
21
Q

Describe the risk factors associated with epithelial ovarian tumours

A
  • Risk factors include BRCA mutations, smoking, endometriosis
  • More ovulations (such as no OCP, early menarche, late menopause) means more damage and healing to ovaries and thus higher chance of mutations
22
Q

Describe the types of epithelial ovarian tumours

A
  • Serous ovarian tumour - often spread to peritoneal surfaces and omentum
    • Commonly associated with ascites
    • Cells can fall off ovary and spread around the body
  • Mucinous ovarian tumour - large cystic masses filled with sticky, thick fluid
    • Usually benign or borderline
    • Pseudomyxoma peritonei - extensive mucinous ascites
      • Epithelial implants on peritoneal surfaces
  • Endometrioid ovarian tumour - contain tubular glands resembling endometrial glands
    • Can arise in endometriosis
    • Some associated with endometrial endometrioid adenocarcinoma
23
Q

Describe germ cell ovarian tumours

A
  • Pluripotent
  • Most are teratomas - usually benign
  • Mature teratomas / dermoid cysts
    • Benign and most common
    • Most are cystic
    • Contain hair, sebaceous material, tooth structures , skin like structures
    • Often tissue from other germ layers
  • Monodermal teratomas - struma ovarii benign but composed of mature thyroid tissue and produces thyroid hormones
24
Q

Describe sex cord-stromal tumours

A
  • Functional tumours as derived from endocrine apparatus of the ovary
  • Most occur in post-menopausal women
  • Sex cord produces Sertoli and Leydig cells in testes and granulosa and theca cells in ovaries
  • Tumours resembling all of these four cell types can be found in the ovary
  • May produce large amounts of oestrogen - precocious puberty in children, breast disease, endometrial hyperplasia in adults
  • May produce masculine features if testosterone levels are high
25
Q

Describe the cause of ovarian metastases

A
  • Most commonly Mullerian tumours - uterus, fallopian tubes, contralateral ovary, pelvic peritoneum
  • GI tumours and breast tumours
26
Q

Describe the classification of testicular tumours

A
  • Germ cell tumours
    • Seminomas
      • Treatment is radiotherapy and radical orchiectomy
    • Non-seminomatous germ cell tumours (NSGCT)
      • Have high hCG and alpha fetoprotein levels in blood
      • Treatment is chemotherapy and surgery (radical orchiectomy)
  • Sex cord-stromal tumours
    • Sertoli and Leydig cell tumours
  • Lymphomas