exam 3 - Gyn Oncology Flashcards

(52 cards)

1
Q

A 67 year old G0, LMP 12 years ago presents with postmenopausal bleeding x 2 weeks. She is using 2 pads/day and denies: heavy vaginal bleeding, pain, dizziness, headache or syncope. Past medical history is significant for HTN, DM. On pelvic exam, you note no abnormal findings except for about 5-10 cc of blood in the vaginal vault. -triage- us

A

Your patient cannot tolerate the endometrial biopsy in the office.
With your supervising MD, you elect to perform dilation and curettage with hysteroscopy in the OR.
Your patient undergoes a total hysterectomy, bilateral salpingo
-oophorectomy and lymphadenectomy.
Pathology reveals stage 1A well
-differentiated endometrioid type endometrial carcinoma.
No adjuvant therapy is indicated.

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2
Q

epidemiology of endometrial cancer and risk factors

A

-About 66,000 cases/year in U.S.
-It is the 8th leading cause of cancer deaths in U.S. cisgender women

-RF:
-Unopposed estrogen
-Chronic anovulation- PCOS
-Exogenous estrogen use
-Selective estrogen receptor modulators (SERMs)- May increase or decrease risk of endometrial CA, depending on SERM
-> For ex. tamoxifen increases the risk of endometrial polyps and endometrial CA
-Obesity
-Family hx (Lynch syndrome, etc.)
-Increasing age
-MC > 50yo
-Low parity or nulliparity
-Early menarche
-Late menopause
-Smoking
-Hx of Lynch syndrome - Increased risk of colorectal CA, endometrial CA and ovarian CA

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3
Q

signs and symptoms - endometrial cnacer

A

MC sx: postmenopausal bleeding (90% of endometrial CA pts).
But only 15-25% of pts with postmenopausal bleeding have CA.
MCC of postmenopausal bleeding: endometrial atrophy.
Other symptoms: pelvic pain, pelvic mass, weight loss.

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4
Q

types of endometrial CA

A

Type 1: Endometrioid adenocarcinoma (75%), usually low grade and limited to uterus at dx.
Type 2: Clear cell and papillary serous tumors, more aggressive.
NEVER NEED TO KNOW STAGING.

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5
Q

natural hx of endometrioid type endometrial carcinoma

A

Progression: simple hyperplasia
-> complex hyperplasia
-> complex hyperplasia with atypia
-> carcinoma

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6
Q

endometrial CA triage

A

Pelvic US with attention to endometrial stripe.
Normal ≤4 mm in postmenopausal bleeding → no bx needed.
>4 mm → endometrial sampling.
No PMB but ≥11 mm → sampling.

-Pelvic US with attention to endometrial stripe (AKA endometrial echo)

-!!Normal: ≤4 mm in pts with hx of postmenopausal bleeding
-Pts with postmenopausal bleeding and this finding on US do NOT need an endometrial bx
-Pts with hx of postmenopausal bleeding and who have an endometrial stripe >4 mm require endometrial sampling (endometrial biopsy or dilation and curettage)
-In pts w/o postmenopausal bleeding, the risk of malignancy increases significantly with an endometrial echo of ≥11 mm -> endometrial sampling

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7
Q

normal

A

Pelvic ultrasound : EM stripe = 1.
48 cm

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8
Q

Hysteroscopy: normal findings in postmenopausal patient. Note R tubal ostium labeled below

A

hysteroscopy in a patient with endometrial CA

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9
Q

surgical managment endometrial cancer

A

-Surgery should be performed with or by a gynecologic oncologist
-Exam under anesthesia
-Peritoneal fluid for cytology

tx: surgical resection
-Total hysterectomy with bilateral salpingo - oophorectomy
- pelvic and para
-aortic lymphadenectomy (check for lymph node spread)
-May be performed by open procedure, laparoscopy or robotic
-assisted laparoscopy
-Ovarian preservation is possible in some premenopausal patients, but the decision must be individualized
-pic: dont need to know

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10
Q

endometrial - adjuvant therapy

A

Radiation reduces recurrence in Stage 1–2 with RF.
Chemo: paclitaxel, doxorubicin, cisplatin or carboplatin.
Hormone: medroxyprogesterone or megestrol acetate for fertility desire or poor surgical candidates.

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11
Q

A 67 year old para 0, LMP 10 years ago, has noted increased abdominal girth and indigestion for the past four months. Two months ago, her PMD suggested she was ‘just getting older’ after exam. On exam, you note a fluid wave and bilateral adnexal masses.

A

Your patient undergoes total hysterectomy, BSO, lymphadenectomy, appendectomy, and omentectomy with cytology and subdiaphragmatic scraping.
Stage 3A epithelial ovarian carcinoma.
Begins chemo with paclitaxel and carboplatin.

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12
Q

ovarian carcinoma

A

Most lethal GYN malignancy.
Etiologies: uninterrupted ovulation, inflammation, tubal CA with early metastasis.
19,000 cases/year.
Lifetime risk 1.2%.
24% have inherited mutation.
70% diagnosed at Stage III.
- 5-year survival 20–30%.
Vague sx.

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13
Q

ovarian CA RF

A

Low parity, age >50, uninterrupted ovulation, family hx, BRCA1/2 (15–45% risk), hx of other adenocarcinomas.

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14
Q

factors that decrease risk of ovarian CA

A

OCPs (risk ↓ by >40–50%), bilateral tubal ligation, bilateral salpingectomy (w/ hysterectomy), prophylactic BSO in high risk pts.

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15
Q

s&s of ovarian CA

A

-abd pain
-abd bloating
-early satiety
-urinary frequency
-increase abd girth
-indigestion
-fatigue
-back pain
-urinary incontinence
-constipation
-pelvic pain
-unexplained wt loss

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16
Q

ovarian CA: histology

A

-Epithelial ovarian carcinoma (70-75% of all ovarian neoplasms, and 90-95% of all ovarian CA)
-Germ cell tumors (15-20% of all neoplasms) -> MC in young pts
-Sex cord-stromal tumors (5-10% of all neoplasms)
-Metastatic tumors -Krukenburg tumors (GI tract)

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17
Q
A

septations ovarian ca

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18
Q
A

large pleural effusion in pt with metastatic ovarian carcinoma

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19
Q

ovarian CA: workup

A

Pelvic mass → pelvic US.
Complex adnexal mass on US→ CT or MRI, labs: CEA, CA-125, AFP.

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20
Q

ovarian CA: surgical staging/debulking procedure

A

-exam under anesthesia
-exploratory laparotomy, peritoneal fluid aspiration, subdiaphragmatic scrapings, total abdominal hysterectomy, bilateral salpingo-oophorectomy, lymphadenectomy, appendectomy, omentectomy
-optimal debulking removes all but <1cm of visible ds, if possible
-if pt is desirous of fertility AND malignancy involves ONLY 1 ovary -> pt may be candidate for unilateral salpingo-ooporectomy w/o hysterectomy

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21
Q

Abridged FIGO staging (dont need to know)

A

Stage 1: ovaries; 2: pelvic extension; 3: peritoneal or lymph node mets; 4: distant mets

22
Q

ovarian CA: adjuvant therapy

A

No radiation.
Standard chemo = taxane + carboplatin.
IV or intraperitoneal.

23
Q

A 38 year old P1001, LNMP unknown, UCG negative, complains of a history of vaginal spotting for four months, notably immediately after intercourse.

A

Colposcopy, ECC, cervical bx → squamous cell carcinoma.
Stage IA.
Undergoes radical hysterectomy.

24
Q

cervical carcinoma epidemiology

A

13,000 new cases/year; 4,000 deaths.
2nd MC cancer worldwide.
HPV is causative.
RF: CIN hx, no screening, high risk HPV, smokers, early sex, multiple partners, STIs, immunosuppression.
Histology: SCC (80%), adenocarcinoma (15%).

25
cervical CA: S&S, dx
-Postcoital bleeding -Serosanguinous vaginal bleeding -Metrorrhagia -Dx: -Colposcopy -ECC, and punch bx of cervix -To determine extent of tumor growth: -US -CT -MRI -PET scan -Nuclear bone scan- pelvic, femur, spine -Laparoscopy -surgical staging: Exam under anesthesia, Cystoscopy, Sigmoidoscopy
26
cervical CA: management
-never need to take out the ovaries for this! -Microinvasive carcinoma: simple hysterectomy without node dissection -> do it vaginally! -Early-stage (stage I-II): -Radical hysterectomy (includes removal of parametria) and lymphadenectomy OR -Primary radiation therapy -Survival rates are similar regardless of method of tx -Late stage (Stage IIb-Stage IV): -Radiation therapy AND chemotherapy -Cisplatin-based chemotherapy -Common sites of metastasis: -Bone -Kidneys, ureters, bladder -Sigmoid and rectum ## Footnote No need to remove ovaries. Microinvasive → simple vaginal hysterectomy. Early stage → radical hysterectomy or RT. Late stage → RT + cisplatin chemo. Mets: bone, urinary tract, GI.
27
Abridged FIGO staging: Cervical CA: dont need to know!
0: in situ. 1: cervix. 2: beyond uterus not to pelvic wall/lower vagina. 3: pelvic wall/lower vagina. 4: bladder/rectum or distant.
28
A 72 year old P2012, LMP 20 years ago presents with a sore on the L labium majus x 6 months. Ulcerated, exophytic lesion, 1.5 x1.5 cm. No inguinal adenopathy.
Radical vulvectomy with inguinal lymphadenectomy → stage II vulvar carcinoma.
29
vulvar carcinoma: epidemiology
5% of GYN malignancies. 6,500 cases/year. MC >60 yo. 15% <40 yo. HPV associated. MC: SCC (90%), melanoma, adenocarcinoma, verrucous, Bartholin’s gland CA, BCC, Paget’s. -MC presents with unilateral lesion with thickened vulvar skin -Pts with Paget’s ds of vulva are at increased risk of colon, breast, and other malignancies
30
vulvar carcinoma S&S
-Persistent vulvar pruritus, especially in postmenopausal women -Nonhealing vulvar ulcer -Most wait 6mo to seek tx -Risk is higher in pts with certain vulvar dermatoses: -Lichen sclerosus -Lichen planus -suspicious of red, white or black lesions -Nonhealing lesions -Use colposcope to better inspect lesions -Biopsy liberally!
31
dx of vulvar carcinoma
Punch bx ± colposcopy. Surgically staged.
32
dont need to know lichen sclerosus
Nonhealing ulcer suspicious for vulvar CA in pt with lichen sclerosus
33
Condylomata -like squamous cell CA of vulva
34
vulvar carcinoma
35
vulvar CA: staging
1: vulva. 2: adjacent structures. 3: perineal + nodes. 4: beyond pelvis.
36
vulvar CA: management
-Squamous cell CA in situ (VIN3): -Local excision -Extensive VIN3 lesions: -Skinning vulvectomy- Vulvar skin is removed and a skin graft is used -Invasive vulvar CA: -Hemivulvectomy in some cases -Radical vulvectomy with lymphadenectomy (inguinal nodes) -Clitoris is spared if not involved in some cases -50% risk of postop infection and/or wound breakdown
37
vulvar CA: adjuvant therapy and sites of metastasis
Radiation Chemo: 5-FU, mitomycin, cisplatin. Mets: lungs, liver, bone.
38
A 29 year old P1001, LMP 2 weeks ago, notes spotting and malodorous bloody discharge x1 mo. Friable mass on posterior vaginal wall.
Stage II vaginal carcinoma → responds to chemo + radiation.
39
vaginal carcinoma epidemiology
Rare (1–3%). 9,000 cses /year. 30% have h/o cervical CA. RF: age >55, hx of CIN or cervical CA, DES exposure in utero
40
vaginal CA: S&S, dx, tx
-Abnormal vaginal bleeding -Dysuria -Urinary frequency -Abnormal findings on PE: -Masses -Ulcerative lesions -Exophytic lesions -Careful and extensive colposcopy is useful -DX: -made via colposcopy and punch Bx of vaginal lesion -Tx: -Radiation therapy- typically -Initially, external beam RT -Next, brachytherapy -Surgical management may be indicated, depending on histologic type and location -May include vaginectomy, partial vaginectomy, or total pelvic exenteration
41
sarcoma botryoides -rare vaginal sarcoma occurring in young girls -grape like polypoid mass protrudes from vaginal introitus
42
vaginal CA: abridged FIGO staging
1: vagina. 2: subvaginal tissue. 3: pelvic wall. 4: bladder, rectum, distant.
43
5 year survival and sites of metastasis: vaginal CA
Stage I: 84%, II: 75%, III–IV: 57%. SCC: 54%, melanoma: 13%, adeno: 60%
44
A 14 yo G1P0, LMP 6 wks ago, with nausea, vomiting, bleeding x5 days (10 pads/24h), tremor, lid lag. Uterus 10 wks size.
Dx: Complete molar pregnancy. Suction curettage (EBL 2L), transfusion. No mets. Later placed on Mirena.
45
Molar pregnancy
-AKA hydatidiform mole or gestational trophoblastic disease -1:1500 pregnancies -Tends to occur at extremes of reproductive life -Choriocarcinoma (placenta CA) can arise from a hydatidiform mole -1:20,000 pregnancies -20% with molar pregnancy will develop choriocarcinoma -Almost 100% curable -Placental site trophoblastic tumors are very rare but can arise after any kind of gestation -dont need to know pic
46
biparental complete moles vs partial moles
biparental complete moles: -Very rare - 45 xx, 45 xy -both maternal and paternal genes are present, but only paternal genes are expressed -due to failure of maternal imprinting and seems to be a genetic, autosomal recessive trait -basically just a placenta -N/V (due to increased bHCG) -Thyrotoxicosis (due to cross-reactivity between thyroxine and HCG) -Pre-eclampsia (before 20 wks!) -Vaginal bleeding and passage of vesicular tissue -Uterine size greater than dates Partial moles: -69, XXX or 69, XXY -Results from duplication of paternal chromosomes or from dispermy - small uterine size - fetus and amniotic fluid present -> missed AB
47
molar pregnancy workup
-Serum quantitative HCG - tumor marker -Sonography -Chest x-ray if pt will have surgery for suspected molar pregnancy -CBC -Type and screen; type and crossmatch -Coagulation studies -Pre-eclamptic labs if the patient has evidence of pre-eclampsia -Dx: -bHCG: usually elevated beyond normal range for pregnancy; may plateau -US: vesicles seen on transvaginal ultrasound -Def dx: pathological analysis of tissue
48
management of molar pregnancy
-Suction curettage -Complications: -Significant blood loss -If pt has pre-eclampsia, may have pulmonary edema and hemoconcentration -If the patient is not desirous of fertility, may have hysterectomy instead -Risk of persistent disease=3-5% regardless of treatment method
49
postop management of molar pregnancy
-Rh immune globulin if Rh negative -F/U pelvic exams for 6-12 months -Evaluate for vaginal metastatic disease -F/U bHCG -q 2 days after surgery -Then q 1-2 weeks while elevated -Then q 1-2 months -Pt must be counseled to use a highly reliable method of birth control x 1 year -> bc how will you know if its a separate pregnancy or a reoccurrance!!
50
nonmetastatic gestational trophoblastic ds v choriocarcinoma
51
management of choriocarcinoma
Methotrexate, Actinomycin D
52
which of the following are the MC used chemotherapeutic agents in the initial management of ovarian carcinoma -paclitaxel and carboplatin!!! -methotrexate and vinblastine -adriamycin and daunorubicin -cisplatin and leucovorin
-paclitaxel and carboplatin!!! -methotrexate and vinblastine -adriamycin and daunorubicin -cisplatin and leucovorin