Neoplasms of the Reproductive System Flashcards
State the type of cancer found in vulva
Squamous cell carcinoma
Describe the epidemiology of vulva tumours
- More commonly found in older women
- 30% of cancers are related to HPV infections
Describe the possible causes of tumours of the vulva
- 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
Describe the epithelium at the cervix
- 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
Describe how HPV can cause cervical cancer
- 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
List the risk factors of cervical cancer
- 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
State the pathology related to cervical tumours
- Cervical intraepithelial neoplasia (CIN)
- Invasive cervical carcinoma
Describe cervical intraepithelial neoplasia and its treatment
- 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
Describe invasive cervical carcinoma presentation and treatment
- 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
Explain the principles of HPV vaccination
- 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
Explain the principles of cervical screening
- 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
Explain endometrial hyperplasia link to endometrial adenocarcinoma
- Endometrial hyperplasia common precursor to endometrial carcinoma
- Increased gland to stroma ratio
- Associated with prolonged oestrogen stimulation (causes proliferation of endometrium)
Explain endometrial adenocarcinoma epidemiology and presentation
- 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
Describe the 2 types of endometrial adenocarcinomas
- 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
Describe the presentation and prognosis of leiomyoma
- 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
Describe a cancerous tumour of the myometrium
- Uterine leiomyosarcoma
- Highly malignant
- Doesn’t arise from leiomyomas
- Commonly metastasize to the lung
Describe the epidemiology of ovarian tumours
- 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
Describe the presentation of ovarian tumours
- 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
Describe the spread of ovarian cancer and how its monitored
- 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
State the classification of ovarian cancer
- Epithelium tumours (Mullerian)
- Germ cell ovarian tumours
- Sex cord-stromal tumours
- Metastases
Describe the risk factors associated with epithelial ovarian tumours
- 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
Describe the types of epithelial ovarian tumours
- 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
Describe germ cell ovarian tumours
- 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
Describe sex cord-stromal tumours
- 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
Describe the cause of ovarian metastases
- Most commonly Mullerian tumours - uterus, fallopian tubes, contralateral ovary, pelvic peritoneum
- GI tumours and breast tumours
Describe the classification of testicular tumours
- 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)
- Seminomas
- Sex cord-stromal tumours
- Sertoli and Leydig cell tumours
- Lymphomas