Cancers Flashcards

1
Q

What type of cancer are vulval cancers usually and how do they commonly appear

A

Usually SCC but can have melanoma and basal cell carcinoma

SCC appear as lumps, ulcers or other skin changes

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2
Q

What are some predisposing factors for vulval cancers

A

Squamous hyperplasia

Lichen sclerosus

VIN

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3
Q

What is vulval intraepithelial neoiplasia

A

In situ precursor of vulval SCC

Is a risk factor for SCC but may or may not develop into SCC

Have atypical squamous cells but no invasion of basement membrane

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4
Q

How is HPV infection related to vulval cancers

A

HPV infection is a cause of VIN and vulval SCC in pre-menopausal women

No relation to HPV in post-menopausal women with VIN or vulval SCC

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5
Q

Where does vulval cancer typically spread to

A

Direct extension: anus, vagina, bladder

Lymph nodes: inguinal, iliac, para-aortic

Distant metastases: lung, liver

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6
Q

Which infection causes cervical cancers, which subtypes and how does it cause cancer

A

HPV infection in the transitional zone

Subtypes 16 and 18 are high risk subtypes

These subtypes produce E6 and E7 proteins that inactive p53 and Rb protein (tumour suppressor genes) -> causes uncontrolled cell growth and proliferation

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7
Q

What is cervical intraepithelial neoplasia

A

Dysplasia of cervical epithelium that does not invade through the basement membrane

Caused by HPV infection

Divided into CIN 1,2,3 with increasing thickness of dysplasia and increasing risk fo progression to invasive SCC

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8
Q

What are the risk factors for CIN and cervical carcinomas

A

Increased risk of exposure to HPV: sexual partner with HPV, multiple partners, early age of 1st intercourse

Multiple births

Early first pregnancy

Smoking

Low socio-economic class

Immunosuppression

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9
Q

How does invasive cervical cancer present, what staging system is used for it and what is the treatment

A

Presentation: post-coital, post-menopausal or inter-menopausal bleeding, may have mass

Uses FIGO staging system

Treatment: hysterectomy, lymph node dissection, chemoradiotherapy

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10
Q

What is endometrial hyperplasia, what are the symptoms and what are the causes

A

Endometrial thickening >11mm. Can be precursor to endometrial cancer

Symptoms are non-specific, e.g. inter-menstrual/post-menopausal bleeding

Caused by excessive oestrogen:

Endogenous - obestiry, early menarche, late menopause, oestrogen secreting tumour

Exogenous - unopposed oestrogen HRT, tamoxifen

Irregular cycles - polycystic ovary syndrome

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11
Q

What are the two types of endometrial cancer and describe their features

A

Endometrioid adenocarcioma - has enlarged glands which appear fused with no visible stroma. Commonly arises from endometrial hyperplasia

Serous carcinoma - more aggressive. Is poorly differentiated. It spreads via transcoelomic spread into peritoneum -> deposits found on peritoneal surface. Has psammoma bodies

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12
Q

How are endometrial cancers managed

A

Hysterectomy

Bilateral salphingo-oophrectomy

Lymph node dissection

Chemoradiotherapy

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13
Q

How do leiomyomata present

A

Asymptomatic

Pelvic pain

Heavy periods

Urinary frequency/GI symptoms due to secondary mass effects

Infertility

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14
Q

What are the symptoms of ovarian cancer

A

Often vague and non-specific

Later symptoms usually caused by mass effect from the tumour

Can have hormonal disturbances

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15
Q

Which tumour marker is used in ovarian cancer and which mutation is associated with ovarian cancer

A

Ca-125 is a serum marker for ovarian cancer

BRCA1/2 mutations

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16
Q

What are the types of ovarian tumours

A

Epithelial tumour

Germ cell tumour

Sex cord stromal tumour

17
Q

Describe the subtypes of ovarian epithelial tumours and how ovarian tumours typically present

A

Ovarian tumours usually present as cystic mass

Serous tumour - highly atypical, pleomorphic cells. Often have psammoma bodies. Spread into peritoneal body via transcoelomic spread

Mucinous tumour - atypical epithelilal cells that secrete mucin

Endometrioid tumour - similar to endometrial endometrioid. Have glands resembling endometrium

Subtypes can be benign, malignant or borderline

18
Q

Describe the subtypes of teratomas (germ cell tumours) and what tumour markers are used for teratomas

A

Mature/dermatoid cyst - benign. Contain fully mature, differentiated tissue from all germ cell layers

Immature - malignant. Contains immature, embryonic tissue

Mono-dermal - contains high specialised, differentiated tissue. Most common is thyroid tissue which is benign but can cause thyroid problems

Markers - AFP, beta-hCG

19
Q

Name some other germ cell tumours, other than teratoma. Are these benign or malignant

A

Are all malignant

Dysgerminoma

Choriocarcinoma

Embryonal carcinoma

Yolk sac tumour

20
Q

Name and describe the two types of sex cord stromal tumours

A

Theca and granuloma cell tumours - produce oestrogen so cause symptoms relating to oestrogen production. Pre-pubtery: precocious puberty. Post-puberty: breast cancer, endometrial hyperplasia/carcinoma

Sertoli-Leydig cell tumours - produce testosterone. Pre-puberty: prevents normal female pubertal changes. Post-puberty: sterility, amenorrhoea, hirsutism, male pattern baldness, breast atrophy

21
Q

What cancers metastasise to the ovary

A

Breast cancer

GI cancers

Gynae cancers - endometrial, ovarian, fallopian

Krukenburg

22
Q

What predisposes a patient to testicular cancer and how does testicular cancer present

A

Cryptorchidism pre-disposes patient to any type of testicular cancer

Patients present with testicular mass +/- pain (usually painless)

23
Q

Which tumours markers are produced by testicular cancers and for which types of testicualr cancer

A

Beta-hCG - choriocarcinoma

AFP - yolk sac tumours

24
Q

What are the types of testicular cancers

A

Germ cell - seminomatous and non-seminomatous

Non-germ cell - sex cord stromal and other

25
Q

Describe testicular germ cell tumours

A

All malignant in post-pubertal males

Have familial predisposition

Cancer in one testis is associated with increased risk of cancer in the other

Divided into seminomas and non-seminomatous germ cell tumours

26
Q

Describe seminomas

A

50% of germ cell tumours

Peak age is 40-50

Often confined to testis for long periods of time

Metastasise to lymph nodes: commonly iliac and para-aortic

27
Q

Describe the types of NSGCTs

A

Yolk sac tumours - occur in young children. Good prognosis

Embryonal carcinomas, choriocarcinomas and mixed NSGCTs occur in young adults

Teratomas - occur in all ages. If pre-pubertal usually benign, if post-pubertal then malignant

28
Q

What is the management of testicular cancer

A

Radical orchiectomy with further treatment depending on whether tumour is seminoma or NSGCT

Seminomas are radiosensitive -> radiotherapy

NSGCTs treated with chemo after surgery

29
Q

What do you look for in histology of cancer biopsies

A

Pleomorphic cells

Hyperchromatic cells

Increased nuclear to cytoplasmic ratio

Irregular nuclear outlines

Coarse speckled/abnormal chromatin appearance