• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/68

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

68 Cards in this Set

  • Front
  • Back

Breast disorders: Key points

Upper outer quadrant has a high density of breast tissue which is why cancer is commonly located here. Also beneath the nipple.




Oestrogen stimulates ductal and alveolar cell growth, fat and stroma, progesterone stimulates alveolar cell proliferation and lobule differentiation for milk production, breast swelling in secretory phase.




Prolactin stimulates lactogenesis and secretion. Oxytocin released by suckling reflex causes expulsion of milk into ducts.




Lymph nodes


- Outer quadrant cancers drain to axillary lymph nodes and inner quadrant cancers drain to the internal mammary nodes.

Nipple discharges

Galactorrhoea


- Mechanical stimulation of nipple due to prolonged sucking, sexual intercourse


- Prolactinoma, most common pathological cause


- Primary hypothyroidism, most common nonpituitary endocrine cause due to increased TRP which stimulates prolactin


- Drugs: OCPs, phenothiazines, methyldopa, H2-receptor blockers, anxiolytics, tricyclic antidepressants (TCAs)




Bloody nipple discharge


- Intraductal papilloma, ductal cancer




Purulent nipple discharge


- Acute mastitis due to S.aureus


- Usually occurs during lactation or breast-feeding


- Treatment, if not methicillin resistant, dicloxacillin or cephalexin. If resistant, co-trimoxazole double strength.




Greenish-brown nipple discharge


- Mammary duct ectasia (plasma cell mastitis)

Breast pain

Most common cause is fibrocystic change


Mondor disease (rare)


- Superficial thrombophlebitis of veins overlying the breast


- Presents as a palpable painful cord

Examples of benign types of micro-calcification in mammograms

Popcorn calcifications




Round calcifications

Fibrocystic change (FCC)

Most common painful breast mass in women <50 years old


Occurs in >50% of women in the reproductive period of life


Distortion of normal cyclic breast changes




Small and large cysts


- Some cysts haemorrhage into the cyst fluid, called blue dome cysts


- Vary in size with menstrual cycle


- No malignant potential


- May have to surgically remove if recurrent




Fibrosis


- No malignant potential




Sclerosing adenosis


- Proliferation of small ductules/acini in the lobule, pattern confused with infiltrating ductal cancer


- Often contains micro-calcifications




Ductal hyperplasia


- Ducts are estrogen sensitive


- Pathological findings, papillary proliferation is called papillomatosis, apocrine metaplasia refers to the presence of large, pink-staining cells, atypical duct hyperplasia increases the risk of developing cancer as it is due to excess oestrogen stimulation



Inflammation

Acute mastitis




Mammary duct ectasia (plasma cell mastitis)


- 25% of women in menopause


- Main duct fills up with debris, causing dilation, rupture and inflammation. Greenish-brown nipple discharge


- May produce skin and nipple retraction simulating cancer


- No increased risk for breast cancer




Treatment


- Antibiotics if infection present


- Surgical removal of blocked duct




Traumatic fat necrosis


- Trauma to breast tissue


- Microscopic findings, lipid-laden macrophages with foreign body giant cells. Fibrosis, dystrophic calcification.


- Painless, indurated mass. (painful in acute stage)


- May produce skin retraction simulating cancer




Silicone breast implant


- Polymer of silica, oxygen and hydrogen


- Silicone gel can leak and implant can rupture, silicone produces foreign body giant cells and chronic inflammation


- Associations with autoimmune disease has not been proved

Benign breast tumours

Fibroadenoma


Phyllodes tumour


Intraductal papilloma

Fibroadenoma

Most common breast tumour in women <35 years old


Most commonly diagnosed breast tumour


Develop in 50% of women who receive cyclosporin after renal transplant




Discrete movable, painless or painful mass


- Multiple lesions may be present (10-15% of cases)




Benign tumour derived from the stroma


- Stroma proliferates and compresses the ducts


- Duct epithelium is not neoplastic


Increases in size during pregnancy


- oestrogen sensitive




May spontaneously disappear or involute during menopause


Do not progress into cancer; however breast cancer may secondarily develop within duct epithelial cells as a separate event (3% of cases)




Diagnosis


- Fine needle or core needle biopsy




Treatment


- Surgical removal


- Cryoablation

Phyllodes tumour

Bulky tumour derived from stromal cells


Most often benign but can be malignant in some cases, hypercellular stroma with mitoses are signs of malignancy


Lobulated tumour with cystic spaces containing leaf-like extensions. Often reaches a massive size.


Treat by wide excision

Intraductal papilloma

Most common cause of a bloody nipple discharge in women <50 years old


Develops in the lactiferous ducts or sinuses


No increased risk for cancer


Surgically remove the duct or sinus

Breast cancer: overview

Most common cancer in adult women (1:8 lifetime risk)


- Mean age is 64 years old


- Risk increases with age




Most common breast mass in women >50 years old




Slightly decreasing in incidence due to early detection and treatment




Second most common cancer-producing death in women, second most common cancer-producing death in adults

Breast cancer: Factors increasing risk

Two main features are:


- Prolonged oestrogen stimulation


- Genetically susceptible background




Increased risk if breast cancer involves first generation relatives


- Mother, sister


Genetic basis is involved in <10% of cases


- Autosomal dominant BRCA1 and BRCA2 association, breast or ovaries are frequently prophylactically removed


- Li-Fraumeni multicancer syndrome, inactivation of p53 tumour suppressor gene




Other gene relationships: RAS oncogene, ERBB2, RB1 suppressor gene




Prolonged oestrogen stimulation


- Early menarche/late menopause


- Nulliparity


- Postmenopausal obesity - aromatisation of androstenedione to estrone


- Hormone replacement therapy


- DCIS, LCIS




Atypical ductal hyperplasia


Endometrial cancer, ionising radiation, smoking cigarettes


High breast density (determined by mammogram)


Recent use of OCPs

Breast cancer: Factors that decrease risk

Breast-feeding


Moderate or vigorous physical training


Healthy body weight

Breast Cancer: Clinical findings and mammography

Clinical findings


- Painless mass in breast, usually in the upper outer quadrant


- Skin or nipple retraction


- Painless axillary lymphadenopathy


- Hepatomegaly, bone pain if metastasis has occurred




Mammography


- Primarily a screening test, detects non-palpable breast masses (80-90% of non-palpable masses)


- Does not distinguish benign from malignant lesions


- Screening usually starts at 40, earlier if patient is at high risk


- Identifies micro-calcifications and and spiculated masses with or without micro-calcification (30-50% of cases). Most often occur in DCIS and sclerosing adenosis (FCC). The following pattern suggests malignancy, five or more tightly clustered microcalcifications that are punctate, micro-linear or branching

Types of breast cancer

Noninvasive


- Ductal carcinoma in situ


- Lobular carcinoma in situ




Invasive


- Infiltrating ductal carcinoma


- Paget disease of nipple


- Medullary carcinoma


- Inflammatory carcinoma


- Invasive lobular carcinoma


- Tubular carcinoma


- Colloid (mucinous) carcinoma

Breast cancer: Natural history, treatment and prognosis

Spread first by lymphatics and then a hematogenous route


- Outer quadrant spreads to axillary nodes


- Inner quadrant cancers spread to internal mammary nodes




Extranodal metastasis


- Common sites for metastasis: lungs, bone, liver, brain, ovaries


- May metastasise 10-15 years after treatment


- Pain in bone metastasis is relieved with radiation




Staging


- Extranodal metastasis has greater significance than nodal metastasis


Sentinel node biopsy (initial node that drains the tumour is sampled), If negative for metastasis, the other nodes in that group are usually negative. If positive for metastasis, there is a 1/3 chance that other nodes in that group have metastases.




Estrogen and progesterone receptor assays (ERA and PRA)


- Most often positive in postmenopausal women


- Clinical significance, confers an overall better prognosis, however, this improvement decreases as the follow-up interval increases


- Candidate for antioestrogen therapy (tamoxifen, oophorectomy)




Other tests performed on tissue


- S phase fraction (>5% is poor prognosis)


- DNA ploidy, diploid tumour is better than an aneuploid tumour


- ERBB2 (HER-2NEU) oncogene status, poor prognosis if amplification or over-expression are present

Breast cancer: Treatment and prognosis

High risk patients without breast cancer


- Treatment with tamoxifen or raloxifene reduces risk




Surgical procedures


- Modified radical mastectomy (nipple/areolar complex, All breast tissue, pectoralis minor, axillary node dissection). Risk of developing winged scapula (long thoracic damage) or lymphadenopathy.


- Breast conservation therapy (lumpectomy with microscopically free margins), sentinel node biopsy and breast irradiation




Prognosis


- Prognosis after curative therapy is dependent on tumour size, extent of nodal metastasis, pathologic grade of the tumour and systemic adjuvant chemotherapy


- Patient with 1 cm tumour with no axillary node involvement has a 10-year disease free survival rate of 90%


- Patient with 3 cm tumour with metastasis in 4 nodes has a 10-year disease free survival rate of 15% if no adjuvant therapy is given


- Outlook for most other is somewhere in between these extremes

Ductal carcinoma in situ (DCIS)

Non-palpable


Patterns: cribriform (sieve-like), comedo (necrotic center)


Commonly contain microcalcifications, cannot be detected by mammogram unless microcalcifications are present


1/3 eventually invade


Treated with lumpectomy

Lobular carcinoma in situ (LCIS)

Non-palpable; virtually aways an incidental finding in a breast biopsy for other reasons; cannot be identified by mammography. (no calcifications)


Lobules are distended with bland neoplastic cells, 1/3 eventually invade, usually positive for oestrogen and progesterone receptors


Increased incidence of cancer in the opposite breast (20-40% of cases)

Infiltrating ductal carcinoma

Stellate morphology (gross specimen and mammogram), indurated, gray-white tumour


1/3 have amplification of the ERBB2 oncogene


Gritty on cut section: induration is caused by reactive fibroplasia (desmoplasia) of the stroma of the tumour

Paget disease of nipple

Extension of DCIS into the lactiferous ducts and skin of the nipple producing a rash, with or without nipple retraction


Paget cells are present


Palpable mass is present in 50-60% of cases

Medullary carcinoma

Associated with BRCA1 mutations


Bulky, soft tumour with large cells and a lymphoid infiltrate


Majority are negative for oestrogen and progesterone receptors

Inflammatory carcinoma

Erythematous breast with dimpling like an orange (peau d'orange) due to fixed opening of the sweat glands, which cannot expand with lymphedema


Plugs of tumour blocking the lumen of dermal lymphatics cause localised lymphoedema


Very poor prognosis


Combination chemotherapy is followed by surgery and irradiation

Invasive lobular carcinoma

Neoplastic cells are arranged linearly or in concentric circles (bull's eye appearance) in the stroma; invasive carcinoma develops in contralateral breast in 5-10% of cases

Tubular carcinoma

Develops in terminal ductules


Increased incidence of cancer in opposite breast (10% of cases)

Colloid (mucinous) carcinoma

Usually occurs in elderly women


Neoplastic cells are surrounded by extracellular mucin

Cervical Pap smear

Purpose - screening test to rule out squamous dysplasia and cancer. To evaluate the hormone status of the woman.




Sample sites


- Vagina, exocervix, TZ




Transformation zone is the site for squamous dysplasia and squamous cancer, it must be adequately sampled. The presence of metaplastic squamous cells or mucus-secreting columnar cells indicates proper sampling. Absence indicates that the smear should be repeated.




Interpretation


- Superficial squamous cells indicate adequate oestrogen


- Intermediate squamous cells indicate adequate progesterone


- Parabasal cells indicate a lack of oestrogen and progesterone


- Normal, nonpregnant adult women have 70% superficial squamous cells, 30% intermediate squamous cells


- Pregnant women - 100% intermediate squamous cells from progesterone effect


- Elderly woman with lack of oestrogen and progesterone, atrophic smear with parabasal cells and inflammation


- Woman with continuous exposure to oestrogen without progesterone, 100% superficial squamous cells. Woman may be taking oestrogen without progesterone or she has a tumour secreting oestrogen. (granulosa cell tumour of the ovary)

Cervical (endocervical polyp)

Nonneoplastic polyp that protrudes from the cervical os


Arises from the endocervix, not the cervix


Most commonly present in perimenopausal women and mutligravida women


Most commonly occurs between 30 and 50 years of age


Not precancerous




Pathogenesis


- Inflammation, trauma and pregnancy




Clinical findings


- Postcoital bleeding, vaginal discharge




Treatment - surgical excision

Cervical intraepithelial neoplasia: Causes

Majority of cases are associated with HPV


- Types 6 and 11 carry a low risk


- Types 16 and 18 carry a high risk


- HPV produces koilocytosis in squamous cells, clear halo with a wrinkled, pyknotic nucleus. Enlarged and hyperchromatic.




Peak incidence is 35 years of age. False negative rate for detecting dysplasia on a cervical pap smear is 40%.




Risk factors:


- Early age of onset of sexual intercourse


- Multiple, high-risk partners


- High-risk types of HPV in a biopsy


- Smoking, oral contraceptive pills (OCPs), immunodeficiency

Cervical intraepithelial neoplasia: Classification, Clinical findings, Treatment

Classification


- CIN I - Mild dysplasia involving the lower 1/3 of epithelium


- CIN II - Moderate dysplasia involving the lower 2/3 of epithelium


- CIN III - Severe dysplasia involving the full thickness of the the epithelium




Progression from CIN I to CIN III is not inevitable


- Reversal to normal is more likely in CIN I


- Requires approx 10 years to progress from CIN I to CIN III


- Requires approx 10 years to progress from CIN III to invasive cancer. Average age for cervical cancer is approx 45 years.




Clinical findings


- Dysplasia is not usually visible under the naked eye and require colposcopy. May see flat to warty condyloma acuminata.


- Colposcopy findings after application of acetic acid include, white areas with punctation, mosaic pattern or abnormal vascularity




Treatment


- Electrocoagulation


- Cryotherapy


- Laser ablation


- Local surgery (conization)

CIN morphology

Hyperchromatic etc.

Cervical cancer

Least common gynaecological cancer and least common gynaecological cancer producing mortality


Higher incidence in developing countries (no easy access to healthcare)




Majority are SCC (75-80% of cases)


- Small cell cancer and adenocarcinoma are less common types


- Cause and risk factors: Same as for CIN




Cervical Pap smears have markedly reduced the incidence and mortality from cervical cancer


- Pap smear detection of low-grade cervical dysplasia had a sensitivity of 70 and spec of 75%


- Pap smear detection of high-grade cervical dysplasia has a sensitivity of 75% and spec of 95%




Clinical findings


- Abnormal vaginal bleeding (most common), usually postcoital


- Malodorous discharge




Cancer characteristics


- Extends down into the vagina


- Extends into lateral wall of cervix and vagina


- Frequently infiltrates the bladder wall and obstructs the ureters, postrenal azotemia leading to renal failure is a common cause of death


- Distant metastasis (e.g. lungs)




Treatment of invasive cancer


- Surgery, radiation or both


- Chemotherapy in selected cases




Prognosis


- 1 and 5 year relative survival rates are 88% and 72%

Endometritis

Definition: Uterine infection following delivery (vaginal/cesarean section) or abortion


Rate of postpartum endometritis (1-8%)


Most common genital tract infection after delivery


More common in preterm deliveries




Acute endometritis


- Most often due to bacterial infection following delivery or miscarriage


- Group B streptococcus (streptococcus agalactiae) is a common pathogen


- Other pathogens: Group A strep, Staphylococcus aureus, Bacteroides fragilis, C.trachomatis, N.gonorrhoea, E.Coli




Clinical findings


- Fever


- Uterine tenderness


- Purulent or foul vaginal discharge (lochia)


- Abdominal pain




Treatment


- Cefoxitin, ticarcillin-clavulanate, ampicillin-sulbactam




Chronic endometritis




Causes


- Retained placenta


- Gonorrhoea, IUD (Actinomyces isrealii)




Key histologic finding is the presence of plasma cells.




Treatment as for acute case

Adenomyosis

Definition - Invagination of stratum basalis into the myometrium




- Glands and stroma thicken myometrial tissue


- Uterus becomes enlarged


- Highest incidence occurs in women in mid to late 40s


- Common finding in hysterectomy specimens




Clinical findings


- Menorrhagia, dysmenorrhoea, pelvic pain




Definitive diagnosis with myometrial biopsy




Treatment


- Hysterectomy

Endometriosis: Overview, pathogenesis and common sites

Definition - Functioning glands and stroma are located outside the uterus, cyclic bleeding of gland and stromal implants wherever they are located.




Prevalence is highest in women with dysmenorrhoea (40-60% of cases)


Average age at time of diagnosis is 25-29 years old


Multifactorial inheritance has been implicated, approximately 7% occurrence rate in first degree-female relatives




Pathogenesis


- Reverse menses through fallopian tubes (most common), implantation of viable endometrial cells


- Coelomic metaplasia


- Vascular or lymphatic spread




Common sites


- Ovaries (most common), rectal pouch, fallopian tubes, intestine

Endometriosis: Clinical findings, Diagnosis and treatment

Clinical findings


- Dysmenorrhoea (most common)


- Abnormal bleeding, premenstrual spotting, menorrhagia


- Painful stooling during menses (bleeding implants on the rectal serosa in the pouch of douglas are stretched with stooling)


- Intestinal obstruction and intestinal bleeding during menses


- Increased risk for ectopic pregnancy


- Infertility, dyspareunia


- Enlargement of ovaries (blood-filled cysts)




Diagnosis


- Laparoscopy useful for diagnosis and treatment, implants have a powder burn appearance


- Increased serum cancer antigen 125 (CA125), excellent sensitivity but poor specificity. More useful in excluding endometriosis when it returns negative.




Treatment


- Combination oral contraceptives


- Progestins (medroxyprogesterone acetate)


- Gonadotrophin-releasing hormone agonists


- Laparoscopic removal of implants

Endometrial polyp

Benign polyp that enlarges with oestrogen stimulation


Does not progress to endometrial carcinoma


Can protrude through cervix into vagina




Clinical findings


- Common cause of menorrhagia in 20-40 year old age bracket


- Spotting occurs between menstrual periods or after menopause




Diagnosis


- Vaginal ultrasound


- Dilation and curettage




Treatment


- Dilation and curettage


- Hysteroscopy

Endometrial hyperplasia: Overview and risk factors





Definition - Endometrial gland hyperplasia due to prolonged, unopposed oestrogen stimulation




Risk factors


- Early menarche or late menopause


- Nulliparous


- Obesity (increased aromatisation of androgens to estrogen in adipose)


- PCOS
- Taking estrogen without progesterone


- Anovulatory menstrual cycles


- HNPCC

Endometrial hyperplasia: Classification, Clinical findings, diagnosis and treatment

Simple hyperplasia


- Increased number of cystically dilated glands


- No glandular crowding




Complex hyperplasia


- Increased number of dilated glands with branching


- Glandular crowding




Atypical hyperplasia


- Glandular crowding and dysplastic epithelium


- Greatest risk for endometrial cancer




Clinical findings


- Menorrhagia, metorrhagia, menometorrhagia


- Postmenopausal bleeding




Diagnosis


- Endometrial biopsy




Treatment


- OCPs


- Medroxyprogesterone acetate


- Hysterectomy if atypia is present

Endometrial carcinoma: Overview

Most common gynaecological tumour


Median age at onset, 60 years old




Pathogenesis


- Prolonged oestrogen stimulation, same risk factors as endometrial hyperplasia


- OCPs decrease risk due to antioestrogen effect of progestins


- Slightly increased risk for breast cancer




Types of endometrial cancer


- Well-differentiated adenocarcinoma, most common type made up of adenocanthoma (contains foci of benign squamous tissue (no prognostic significance) and adenosquamous carcinoma (contains foci of malignant squamous cancer (worse prognosis)




- Papillary adenocarcinoma (highly aggressive cancer)




Cancer characteristics


- Spreads down into the endocervix


- Spreads out into the uterine wall


- Lungs are the most common site of metastasis




Clinical findings


- Postmenopausal bleeding (90% of cases)




Diagnosis


- Endometrial biopsy




Treatment


- Surgery, radiation, hormones (tamoxifen), or chemotherapy depending on stage

Leiomyoma (fibroids)

Benign smooth muscle tumour


Most frequently diagnosed gynecologic tumour


Occurs in 20-50% of women >30 years old


More common in blacks than whites


Estrogen-sensitive tumours (may become larger during pregnancy)




Tumour characteristics


- Commonly undergo the following


1) Degeneration


2) Dystrophic calcification


3) Hyalinisation (reason for the term fibroids)




Rarely transform into leiomyosarcomas (<1% of cases)




Clinical findings


- Menorrhagia (when located in submucosa)


- Obstructive delivery


- Cramping during menses


- Pressure on colon (constipation)


- Pressure on bladder (increasing frequency, urgency, incontinence)




Diagnosis


- Transabdominal or transvaginal ultrasound


- MRI




Treatment


- Myotomy for women who want to preserve fertility


- Hysterectomy

Ovarian tumours: Overview and risk factors

Tumours are more likely benign if <45 years of age


- Risk increases with age


- Median age of presentation is 61 years of age


- Incidence peaks in women in their late 70s


- Approximately 60% present with advanced disease




Risk factors


- Nulliparity (greater number of ovulatory cycles increases risk), risk for surface-derived ovarian tumours is increased




- Genetic factors - BRCA1 and BRCA2 suppressor genes, Lynch syndrome, Turner syndrome increased risk for dysgerminoma. Peutz-Jeghers syndrome, increased incidence of ovarian sex cord tumours.




- History of breast cancer




- Postmenopausal oestrogen therapy, obesity (increased oestrogen)




- OCPs/pregnancy decrease risk for surface-derived ovarian cancers as they decrease number of ovulatory cycles

Classification of ovarian tumours

Surface-derived tumours


- Account for 65-70% of ovarian tumours


- Derive from coelomic epithelium


- Account for the greatest number of malignant ovarian tumours


- Malignant tumours commonly seed the omentum




Germ cell tumours


- They account for 15 - 20% of ovarian tumours


- Cancers are similar to those seen in the testicle


- A relatively small number of germ cell tumours are malignant




Sex cord-stromal tumours


- Account for 3-5% of ovarian tumours


- Derives from stromal cells


- Some of these are hormone producing (granulosa cell tumour produces oestrogen)


- Majority of these tumours are benign




Metastasis


- Accounts for 5% of ovarian tumous


- Majority are haematogenous metastasis; seeding is less common


- Common primary cancers metastasising to ovaries include mullerian origin from uterus, fallopian tubes, contralateral ovary. Extramullerian origin from breast, GI tract. Krukenberg tumour is unique in that signet ring cells and present and implicate diffuse cancer of the stomach or breast cancer as the primary site.

Ovarian tumour: Clinical findings

Abdominal enlargement due to fluid (most common sign)


- Malignant ascites is most often due to seeding


- Signs of malignant ascites due to seeding include induration in the rectal pouch on DRE. Intestinal obstruction with colicky pain.




Palpable ovarian mass in a postmenopausal woman


- Ovaries should not be palpable in menopausal women because they are atrophic




Malignant pleural effusion


- Pleural cavity is a common site for ovarian cancer metastasis




Cystic teratomas undergo torsion leading to infarction


- Radiographs show calcification from bone and/or teeth




Signs of hyperestrinism from oestrogen-secreting tumours


- Bleeding occurs from endometrial hyperplasia/cancer


- 100% superficial squamous cells are present in a cervical Pap smear




Hirsutism or virilisation is associated with androgen-secreting tumours


- Sertoli-Leydig cell tumour







Ovarian tumour: Tumour markers, Treatment and Prognosis

Tumor markers


- Cancer antigen 125 (CA125)


- Only increased in surface-derived malignant tumours




Treatment


- Surgery, chemotherapy, occasionally radiation




Prognosis


- Better prognosis if <65 years old


- Overall 1- and 5- year relative survival rates for ovarian cancer are 75% and 45% respectively.





Surface derived tumours

Serous tumours


Mucinous tumours


Endometrioid


Brenner tumour

Serous tumours

Most common group of primary benign and malignant tumours


Most common group of tumours that can be bilateral


Cysts are lined by ciliated cells (similar to the fallopian tube)




Serous cystadenoma: benign and most common benign ovarian tumour




Serous cystadenocarcinoma: malignant. Has psammoma bodies (dystrophically calcified tumour cells)

Mucinous tumours

Cysts are lined by mucus-secreting cells (similar to endocervix)


Large, multiloculated tumours


Seeding may produce pseudomyxoma peritonei (most common primary site for pseudomyxoma peritonei is not mucinous tumours of the ovary but mucinous tumours of the appendix)




Mucinous cystadenoma: benign, may be associated with Brenner tumour




Mucinous cystadenocarcinoma: Malignant

Endometrioid

Malignant tumours that are commonly associated with endometrial carcinoma (15-30% of cases); tumour resembles endometrial carcinoma.




Commonly bilateral

Brenner tumour

Usually benign


Contain Walthard cell rests (transitional-like epithelium)



Cystic teratoma

Most are benign; <1% become malignant (usually squamous cancer)


Most common benign germ cell tumour; contain ectodermal (e.g. hair), mesodermal (muscle), and endodermal tissues (thyroid); ectodermal differentiation (hair, sebaceous glands and teeth) is the most prominent component.


Most of these derivatives are found in a nipple-like structure called Rokitansky tubercle.


Immature malignant types contain mature and immature components (muscle, neuroepithelium)


Struma ovarii type has functioning thyroid tissue and will take up radioactive iodine-123

Dysgerminoma

Most common malignant germ cell tumour; same histologic appearance as a seminoma of the testis. Characteristic increase in serum LDH.




Associated with the streak gonads of Turner syndrome.

Yolk sac tumour

Malignant tumour (similar to yolk sac tumour in males)


Most common ovarian cancer in girls <4 years old; however, the average age of occurrence of the tumour is 23 years old


Contain Schiller-Duval bodies (resemble yolk sac)


Increased serum alpha-fetroprotein

Thecoma-fibroma

Benign tumour associated with Meigs syndrome (ascites, right-sided pleural effusion); regression of effusions follows removal of tumour




Commonly calcify

Granulosa-theca cell tumours

Low-grade malignant tumour


Feminising tumour (produces estrogen) that contains Call-Exner bodies

Sertoli-Leydig cell tumour

Benign masculinising tumour (produces androgens)


Pure Leydig cell tumours contain cells with crystals of Reinke


Association with Peutz-Jehgers syndrome



Gonadoblastoma

Malignant tumour with mixture of a germ cell tumour (dysgerminoma) and sex-cord stromal tumour


Associated with abnormal sexual development in 80% of cases


Commonly calcify

Metastasis from mullerian tumours or extramullerian tumours

May effect one or both ovaries; usually haematogenous spread; less commonly due to seeding


Mullerian origin - uterus, fallopian tubes, contralateral ovary


Extra-mullerian origin - breast, GI tract

Krukenberg tumour

May affect one or both ovaries


Contains signet-ring from haematogenous spread of a gastric cancer (diffuse carcinoma with linitus plastica); breast cancer also metastases to the ovaries (some breast cancer variants have signet ring cells)

Vulval intra-epithelial neoplasia

Dysplasia ranges from mild to carcinoma in situ (CIS)


Strong association with HPV type 16


Precursor for developing SCC

Squamous cell carcinoma of the vulva

Most common cancer




Risk factors:


- HPV type 16


- Smoking cigarettes


- Immunodeficiency




Affects all vulvar structures.




Metastasise first to the inguinal nodes

Extramammary Paget Disease

Red, crusted vulvar lesion


Intraepithelial adenocarcinoma


- Tumour derives from primitive epithelial progenitor cells


- Malignant Paget cells contain mucin which is periodic acid-Schiff positive


- Spread along the epithelium (rarely invades the dermis)

Non-neoplastic dermatoses of the vulva

Lichen sclerosus


- Usually occurs in postmenopausal women


- Thinning of the epidermis, parchment like appearance of the skin


- Small risk for developing squamous cell carcinoma (SCC)




Lichen simplus chronicus


- White plaque-like lesion (leukoplakia), due to squamous cell hyperplasia


- Small risk for developing SCC

Vaginal tumours

Rhabdomyoma


Embryonal rhabdomyosarcoma


Clear cell adenocarcinoma


Vaginal squamous cell carcinoma

Rhabdomyoma

Benign tumour (hamartoma?) of skeletal muscle


Other locations are the tongue and heart (associated with tuberous sclerosis)

Embryonal rhabdomyosarcoma

Most common sarcoma in girls


- Malignancy of skeletal muscle (rhabdomyoblasts with striations)


Occurs in girls <5 years old


Necrotic, grape-like mass protrudes from the vagina

Clear cell adenocarcinoma of the vagina

Occurs in women with intrauterine exposure to diethylstilboestrol, was used to prevent a threatened abortion


DES inhibits mullerian differentiation, these include the fallopian tubes, uterus, cervix, upper 1/3 of vagina




Vaginal adenosis


- Benign remnants of mullerian glands which produces red, superficial ulcerations in the upper portion of the vagina


- Precursor lesion for clear cell adenocarcinoma




Risk for developing cancer is small (1/1000)




Cancer involves the upper vagina




Other DES abnormalities


- Abnormally shaped uterus that thwarts implantation


- Cervical incompetence, common cause of recurrent abortions







Vaginal squamous cell carcinoma

Primary SCC is associated with HPV 16


Most cancers are an extension of a cervical SCC into the vagina


Primary cancers metastasise to the inguinal lymph nodes