Prevention and Screening and Gynecologic Cancers Flashcards

1
Q

top causes of female morbidity and mortality for all ages

A
    1. Heart Disease
    1. Cancer
    1. Cerebrovascular events
    1. COPD
    1. Pneumonia, Influenza
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2
Q

female mobidity and mortality by age

A
  • Ages 15-34 years
      1. Accidents
      1. Cancer
      1. Homicide/Suicide
  • Ages 35-54 years
      1. Cancer
      1. Heart Disease
      1. Accidents
  • Ages 55-74 years
      1. Cancer
      1. Heart Disease
      1. COPD
  • Age 75 years and over
      1. Heart Disease
      1. Cancer
      1. Cerebrovascular events
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3
Q

disease prevention

A
  • Cervical Cancer → Pap smear, HPV vaccine
  • Breast Cancer → Mammogram
  • Skin Cancer → Physical exam, SPF use
  • Colorectal Cancer → Hemoccult testing, Colonoscopy
  • Anemia → Hemoglobin, Hemoglobin electrophoresis
  • Counseling to reduce risk factors – safe sex practices, using SPF/sun exposure, diet and exercise, healthy BMI, smoking cessation, etc.
  • Coronary Artery Disease → lipid profile, BP screening, smoking cessation, ASA
  • Thyroid Disease → TSH
  • Sexually Transmitted Infections → HPV vaccine, screening
  • Diabetes → FBS, Hgb A1c, diet/exercise
  • Osteoporosis → bone density (DXA) scan, wt bearing exercise, Ca/vit D supplements
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4
Q

well women exam

A
  • History
    • Menstrual history: menarche, LMP, menopause, abnormal bleeding, symptoms
    • Obstetric history: GaPbcde, OB complications
    • Gynecologic history: gynecologic diseases, surgeries, STI history, breast disease, urinary complaints
    • Sexual and contraceptive history: number of partners, history of sexual abuse, contraception used
  • Immunizations
  • G=pregnancies; P=outcomes of pregnancies (b=term deliveries, c=premature deliveries, d=abortions, e=living children)
  • Immunization recommendations: cdc.gov
  • No evidence exists of risk to the fetus from vaccinating pregnant women with inactivated virus or bacterial vaccines or toxoids. In spite of the lack of evidence of risk, HPV vaccine, an inactivated vaccine, is not recommended during pregnancy. Live vaccines administered to a pregnant woman pose a theoretical risk to the fetus; therefore, live, attenuated virus and live bacterial vaccines generally are contraindicated during pregnancy. Women should avoid conception for 4 weeks after vaccination with live vaccines. However, benefits of vaccinating pregnant women usually outweigh potential risks when the likelihood of disease exposure is high, when infection would pose a risk to the mother or fetus, and when the vaccine is unlikely to cause harm.
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5
Q

immunizations

A
  • Tetanus-diphtheria (Td or TDaP)
    • Every 10 years from age 11 years
    • Pregnancy in 3rd trimester (27-36 wks) of each pregnancy – INCLUDING PERTUSSIS!! GET TDAP
    • Anyone who has questionable vaccine history and current high-risk injury
    • TDaP (including pertussis) once in adulthood
  • HPV
    • HPV types vary depending on brand/formulation
    • Ages 9-26 years; start at 11-12 yr visit
    • 2 dose series given 6-12 months apart
    • Not recommended for use in pregnancy at this time
  • Cervarix = HPV vaccine types 16 & 18 only
  • Gardasil = HPV vaccine types 6, 11, 16, 18
  • Gardasil 9 = HPV vaccine types 6, 11, 16, 18, 31, 33, 45, 52, 58
  • Influenza
    • Yearly for everyone
    • Inactivated vaccine for any women who is or will be pregnant during flu season
  • Pneumococcal
    • All adults age 65 and older should get vaccinated with PCV13 and PPSV23, 1 year apart
    • Adults at high risk should be vaccinated once with each vaccine
  • MMR
    • Everyone should have 2 doses by the age of 6 years
    • Required for school entrance
    • All women of childbearing age unable to show proof of Rubella immunity with titers
    • Live virus not indicated during pregnancy
  • Hepatits B
    • IVDA, health care workers, current recipients of blood products, Hepatitis C, prostitutes
    • 3 dose series, given at 0, 4 weeks and 8 weeks
    • Now required for school entrance in most areas
    • At postpartum visit if not immune
  • Hepatitis A
    • Two-dose series, given 6 months apart
    • Recommended in endemic areas, not yet required for school entrance except in some border areas
  • Varicella/Zoster
    • Recommended for anyone not previously exposed to chicken pox
    • 2 doses given 4-8 weeks apart
    • Live virus not indicated during pregnancy
    • Zostavax available for adults >50 years of age, given routinely at age 60
  • PPD (TB skin testing)
    • Every 2 years for high-risk individuals
    • Should be considered in any patient with a cough lasting >4 weeks
    • Should be placed at the first prenatal visit
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6
Q

Vaccines for Pregnant women

A
  • Women who are pregnant should receive a dose of Tdap for the prevention of infant pertussis whether or not they have previously received Tdap. Vaccination of the mother generates antibodies that pass transplacentally to the fetus. Vaccination in the third trimester optimizes the duration of this antibody protection until after birth. Additionally, preventing pertussis in the mother reduces the risk that the infant is exposed to pertussis after birth. Health care personnel should administer Tdap during pregnancy, preferably during the third trimester. If Tdap is not administered during pregnancy to women who have never received it, it should be administered immediately postpartum. Pregnant women who are not vaccinated or are only partially vaccinated against tetanus should complete the primary series. Women for whom Td is indicated but who did not complete the recommended 3-dose series during pregnancy should receive follow-up after delivery to ensure the series is completed. One dose of the tetanus vaccine series should be Tdap, if Tdap has not already been received.
  • Pregnant and postpartum women are at higher risk for severe illness and complications from influenza than women who are not pregnant. Pregnant women have protective levels of anti-influenza antibodies after vaccination. Passive transfer of anti-influenza antibodies that might provide protection from vac­cinated women to neonates has been reported. Routine vaccination with inactivated influenza vaccine is recommended for all women who are or will be pregnant (in any trimester) during influenza season.
  • PCV13 = Pneumococcal Conjugate Vaccine (Prevnar); PPSV23 = Pneumococcal Polysaccharide Vaccine (Pneumovax)
  • Pregnant women should be evaluated for evidence of immunity to rubella and varicella and be tested for the presence of HBsAg during every pregnancy. Women without evidence of immunity to rubella and varicella should be vaccinated immediately after delivery.
  • A woman found to be HBsAg positive should be followed-up carefully to ensure that the infant receives HBIG and begins the hepatitis B vaccine series no later than 12 hours after birth and that the infant completes the recommended hepatitis B vaccine series on schedule (20). No known risk exists for the fetus from passive immunization of pregnant women with immune globulin preparations.
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7
Q

physical exam for well woman exam

A
  • Height, Weight, BMI; BP, pulse; LMP
    • Think of LMP as a vital sign for pregnant women
  • Urinalysis, UPT if indicated
    • You get urinalysis on pregnant women, but women who are not pregnant only get it if indicated
    • Infections in pregnant women can cause preterm labor
  • FBS or Hgb if indicated
  • Laboratory tests: TSH, lipid profile, CBC, Chemistry panel as indicated
  • Breast exam and lymph nodes
  • Chest (CV and Respiratory)
  • Pelvic exam, including exam of abdomen and lymph nodes
    • Bimanual exam
    • Collection of samples for STI testing, Pap smear
    • Rectovaginal exam, including guaiac testing if indicated (women who are over 50, retroflexed uterus, etc.)
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8
Q

Well woman exam: counseling and education

A
  • Diet and exercise
  • STI prevention
  • Contraception use, hormone therapy
  • (Self breast exam)
  • Skin self exam and SPF use
  • Smoking cessation, EtOH use
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9
Q

vulvar neoplasia

A
  • 4th most common gynecologic cancer
  • 5% of malignancies of female genital tract
  • Most frequently in postmenopausal women
  • Risk factors include smoking, vulvar dystrophy (eg, lichen sclerosus), vulvar or cervical intraepithelial neoplasia, HPV infection, immunodeficiency syndromes, a prior history of cervical cancer, and northern European ancestry
  • The most useful means of generating a differential diagnosis of vulvar lesions is by morphologic findings rather than by symptomatology, which is often nonspecific. In all patients, one or more vulvar biopsies should be performed if the lesion is clinically suspicious for malignancy (asymmetry, border irregularity, color variation, rapid change, bleeding, non-healing). Additional indications for biopsy are if a diagnosis cannot be made confidently by visual inspection and noninvasive methods, if the lesion does not resolve after standard therapy, or to address patient concern. Any lesion on the vulva that is not known to be benign warrants biopsy. An ulcerative lesion that does not heal may need additional and more extensive biopsy despite an initial negative office biopsy result.
  • Two independent pathways of vulvar carcinogenesis are felt to currently exist:
    • mucosal HPV infection
    • chronic inflammatory (vulvar dystrophy) or autoimmune processes
  • HPV has been shown to be responsible for 60% of vulvar cancers
    • HPV 16 and 33 are the predominant subtypes accounting for 55.5% of all HPV-related vulvar cancers
  • 90% squamous cell carcinomas; other histologies include melanoma, Bartholin gland adenocarcinoma, sarcoma, Paget disease, or basal cell carcinoma
    • Squamous is slow growing and destroys locally
  • Classification:
    • VIN-I, mild dysplasia
    • VIN-II, moderate dysplasia
    • VIN-III, severe dysplasia or carcinoma in situ
  • VIN-I and VIN-II are likely to progress to CIS or carcinoma
  • Lesions are normally localized and isolated
  • Melanoma is the second most common type of vulvar cancer. Lesions typically arise de novo on the clitoris or labia minora, but can also develop within preexisting junctional or compound nevi
  • Extramammary Paget disease (an intraepithelial adenocarcinoma) and basal cell carcinomas are associated with a high incidence of antecedent or concomitant malignancy elsewhere in the body.
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10
Q

Dds: vulvar cancer

A
  • epidermal inclusion cysts
  • lentigos
  • disorders of Bartholin gland
  • acrochordons
  • hidradenomas
  • seborrheic keratoses
  • lichen sclerosus
  • other dermatoses
  • condyloma acuminate
  • If one of these disorders is initially suspected but does not respond to appropriate treatment, biopsy should be performed
  • **UpToDate: Vulvar lesions: Differential diagnosis based on morphology
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11
Q

Ddx: vulvar lesions

A
  • Flesh colored lesions: sebaceous glands, vestibular papillae, skin tags, cysts, and infections (warts, molluscum contagiosum)
  • White lesions: lichen sclerosus, lichen simplex chronicus, and vitiligo
  • Brown, black, or red vulvar lesions can be due to a wide variety of benign, infectious, inflammatory, and malignant conditions
  • Pustules, vesicles, and erosions are usually related to infection or inflammation
  • Ulcers and fissures can be caused by infection, malignancy or systemic disease with vulvar involvement
  • We recommend that any atypical-appearing dark lesion be biopsied to exclude premalignant or malignant lesions
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12
Q

diagnosis of vulvar neoplasia

A
  • Pt c/o vulvar pruritis, chronic irritation, development of raised mass lesions
  • Diagnosis is made by biopsy
  • Any suspicious lesion, chronic pruritis, lesion that does not resolve with standard treatment should be biopsied
    • may use colposcopy for better visualization
    • Vulvar pruritus is the most common symptom of vulvar cancer and a unifocal vulvar nodule, plaque, ulcer, or mass (fleshy, nodular, or warty) on the labia majora is the most common physical finding
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13
Q

vulvar cancer

A
  • Staging using TNM & FIGO criteria (FIGO: International Federation of Gynecology and Obstetrics)
  • Treatment is primarily surgical
    • Wide local excision
    • Inguinal/femoral lymphadenectomy
    • Chemoradiation as adjunct or for advanced disease
  • 5-year survival 70% - 90% for localized disease, 20% if deep pelvic nodes are involved
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14
Q

vulvar paget disease

A
  • Extensive intraepithelial disease
  • Not common (<1%)
  • May be associated with carcinoma of the skin
  • Higher incidence of internal carcinoma, particularly of the colon and breast
  • Treatment is wide local excision or simple vulvectomy and wide margins to prevent recurrence
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15
Q

vulvar melanoma

A
  • Raised, irritated, pruritic, pigmented lesion
  • 5% of all vulvar malignancies
  • Wide local excision is required for diagnosis and staging
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16
Q

vaginal cancer

A
  • Rarest of all gynecologic cancers
  • Same risk factors as in cervical neoplasia
  • Often associated with other lower genital tract neoplasms
  • Most common in women >55 years of age
  • Squamous cell carcinoma in 95% of cases
  • Risk Factors: increased risks for HPV infection
    • Early sexual activity
    • High lifetime number of sexual partners
    • Infection with HIV
    • Smoking
    • Long-term use of oral contraceptives (>5 years)
    • Low socio-economic status
  • Most common c/o is vaginal bleeding
    • Vulvar MC complaint is itching
  • Posterior wall of the upper 1/3 of the vagina is most common site of the tumor; red ulcerated or white hyperplastic lesions
  • Colposcopy with directed biopsy for definitive diagnosis
  • Treatment includes surgical excision; chemoradiation for invasive disease
  • 5-year survival is 50% - 80% with local disease
17
Q

Endometrial (uterine) cancer

A
  • Most common gynecological cancer in US
  • Adenocarcinoma of the endometrium is the most common type of uterine cancer (more aggressive)
    • Lynch syndrome (hereditary nonpolyposis colon cancer) is a genetic syndrome associated with high risk of uterine cancer as well as other types of cancer – BOARD QUESTION
  • Average age at diagnosis is 61 yrs, most women are early stage at diagnosis
  • Risk Factors
    • Use of unopposed estrogen after menopause
    • Overweight women (high BMI)
    • Nulliparity
    • Tamoxifen therapy
  • Protective Factors
    • Childbearing, esp if last pg at older age
    • Combination oral contraceptives
    • Combination hormone replacement
  • Screening Tools
    • None
  • Effectiveness of Early Detection
    • Unknown
  • Cardinal symptom is abnormal uterine bleeding
    • Occurs in 90% of cases
    • 5-20% postmenopausal women with abnormal uterine bleeding have endometrial cancer
  • Endometrial cells on Pap smear in women ≥40 years of age need further evaluation (if they haven’t had their period in the last week)
18
Q

Diagnosis of endometrial cancer

A
  • Diagnosis must be histological – need tissue
  • Endometrial sampling
    • Endometrial biopsy is gold standard for diagnosis
  • Transvaginal US
    • Thickened endometrium (>4-5mm) worrisome
    • 20mm is the mean endometrial thickness for pts with cancer
  • Sonohysterography
    • Filling endometrial cavity with fluid (saline usually) to visualize focal lesions for biopsy
  • Postmenopausal women with abnormal bleeding will need biopsy with or without US, NEED BIOPSY
  • Endometrial sampling is the gold standard for evaluation for endometrial neoplasia. For postmenopausal women, transvaginal ultrasound evaluation of endometrial thickness may be used as an initial study to evaluate for endometrial neoplasia in selected women. For these women, it is reasonable to defer endometrial sampling if the endometrial thickness is <4 mm. However, if postmenopausal bleeding persists, endometrial sampling should be performed. Sonography is not a valid alternative to endometrial sampling in premenopausal women. Evaluation for a nonendometrial source of bleeding, such as cervical, fallopian tube or ovarian cancer, should also be pursued.
19
Q

endometrial biopsy (EMB)

A
  • Gold standard for diagnostic evaluation of all women with abnormal uterine bleeding in whom endometrial hyperplasia or carcinoma is a possibility
  • Evaluation of the endometrium for malignant and premalignant disease
    • Abnormal uterine bleeding
    • Postmenopausal bleeding
    • Abnormal PAP with atypical cells favoring endometrial origin
  • Done with minimal to no cervical dilation
  • Anesthesia is generally not required
  • The cost is 1/10 that of hospital D&C
  • Excellent correlation between histopathology of endometrial specimens taken by biopsy instruments in the office and D&C
  • 99.6% detection rate for endometrial cancer in postmenopausal women
  • Endometrial biopsy
20
Q

Sonohysterography

A
  • Used to evaluate endometrium
  • SIS = saline infusion sonohysterogram
  • Hysteroscopy is a procedure in which a telescope with a camera is used to evaluate or treat pathology of the endometrial cavity, tubal ostia, or endocervical canal. During hysteroscopy, the uterus is distended with a gas or fluid medium. Most diagnostic and brief or minor operative procedures can be performed without anesthetic or with a local anesthetic. In women undergoing hysteroscopy under local anesthetic, we suggest a paracervical block over other methods of administering local anesthesia.
21
Q

endometrial cancer

A
  • Total extrafascial hysterectomy with bilateral salpingo-oophorectomy (TAH-BSO) for staging
  • Pelvic and extended para-aortic lymph node dissection
  • Treatment depends on stage of cancer
  • Surgery alone is usually curative for women who are at a low risk of disease persistence or recurrence
  • Women with intermediate- or high-risk disease may benefit from adjuvant therapy
  • Five-year survival rates for localized, regional, and metastatic disease are 96%, 67%, and 17%, respectively
  • CA-125 tumor marker can be followed in some women
  • Obesity is greatest risk factor for recurrence
  • For women with endometrial carcinoma, surveillance consists mainly of monitoring for symptoms and physical examinations.
  • The majority of recurrences of endometrial carcinoma occur within three years after treatment and are fairly evenly distributed between vaginal/pelvic and distant (abdominal or lung) metastases. The most common sites of recurrent disease are the vaginal vault, pelvis, abdomen, and lungs.
22
Q

ovarian cancer

A
  • 2nd most common GYN cancer in US
    • Lifetime risk 1.4%
    • Higher risk in hereditary cancer syndromes
  • Most common cause of GYN cancer death
  • Average age at diagnosis is 63 yrs
  • 95% of ovarian cancers are epithelial cell origin
  • Risk Factors
    • Age >60 years
    • Family history of ovarian or other gynecologic cancer
    • Hereditary cancer syndrome
    • Smoking
  • Protective Factors
    • Childbearing
    • Combination oral contraceptives
    • Breastfeeding
    • Tubal ligation
    • Hysterectomy
  • Screening Tools
    • Pelvic exam can detect ovarian cancer
      • Cancer usually advanced by the time it can be palpated
    • CA-125 serum marker
    • TVUS may be useful
    • USPSTF recommends against routine screening (2012)
  • Effectiveness of Early Detection
    • 5-year survival rate is 89% for localized disease
    • 36% for women with regional metastases
    • 17% for women with distant metastases
  • Most women aged 40-65 years at diagnosis
  • Vague, nonspecific symptoms
    • Abdominal or pelvic pain, abdominal distention, nausea, constipation, anorexia, etc.
    • Palpation of adnexal mass usually leads to further evaluation for ovarian cancer, but is too advanced
  • US is the initial diagnostic study, followed by CT abdomen/pelvis
  • Serum CA-125 marker elevated in >80% of patients
  • Surgical removal of the ovary necessary for diagnosis, staging and treatment
  • Surgical management primarily, adjuvant therapy depends on stage
  • Survival rates low, depend on residual tumor volume
23
Q

Ddx pelvic mass

A
  • Adnexal Mass
    • Ovarian malignancy
    • Ovarian cyst
    • Ectopic pregnancy
    • PID with TOA
    • Pelvic kidney
    • GI etiology
      • Crohn’s disease
      • Diverticulitis
      • GI neoplasm
  • Central Pelvic Mass
    • Intrauterine pregnancy
    • Leiomyomata (fibroids)
    • Uterine malignancy
    • Bladder malignancy
    • Ovarian malignancy
24
Q

Risk factors for breast cancer

A
  • Age >40 years and increases with age
  • Family h/o breast cancer (BRCA genes)
  • Menarche <12 yrs of age or >40 menstrual yrs
  • Oral contraceptive use >5 years
  • Nulliparity or first delivery >35 yrs of age
  • Obesity
  • Other types of cancer, including contralateral breast, uterus, ovary, salivary gland, colon
25
Q

screening tools for breast cancer

A
  • (Self breast exam)
  • Annual breast exam by a health care professional
    • Insufficient evidence for or against
  • Mammogram – recommendations evolving, based primarily on “Gail Model” or other risk prediction model
    • General recommendation screen women 50-74 years old every 2 years; younger and older women based on individual risk
26
Q

USPSTF recommendations for breast cancer screening

A
  • The USPSTF recommends biennial screening mammography for women aged 50 to 74 years. Grade: B recommendation.
  • The decision to start screening mammography in women prior to age 50 years should be an individual one. Women who place a higher value on the potential benefit than the potential harms may choose to begin biennial screening between the ages of 40 and 49 years. Grade: C recommendation.
  • The USPSTF concludes that the current evidence is insufficient to assess the additional benefits and harms of screening mammography in women 75 years or older. Grade: I Statement.
  • The USPSTF concludes that the current evidence is insufficient to assess the benefits and harms of digital breast tomosynthesis (DBT) as a primary screening method for breast cancer. Grade: I Statement.
  • The USPSTF concludes that the current evidence is insufficient to assess the balance of benefits and harms of adjunctive screening for breast cancer using breast ultrasonography, magnetic resonance imaging, DBT, or other methods in women identified to have dense breasts on an otherwise negative screening mammogram. Grade: I Statement.
27
Q

effectiveness of early detection of breast cancer

A
  • 5-year survival approaches 90% with local disease
  • Survival rates drop to 50% - 70% when regional involvement, <50% with metastatic disease
  • 50% patients have axillary node involvement at time of dx
28
Q

cervical cancer

A
  • 3rd most common gyn cancer
  • Lifetime risk <1%
  • Mean age at diagnosis 48 yrs
29
Q

HPV link to cervical cancer

A
  • HPV central to development of cervical neoplasia
    • 99.7% of cervical ca due to HPV infection
  • 70% are squamous cell carcinoma, 25% are adenocarcinoma
30
Q

Risk factors: increased risks for HPV infection

A
  • Early sexual activity
  • High lifetime number of sexual partners
  • Infection with HIV
  • Smoking
  • Long-term use of oral contraceptives (>5 years)
  • Low socio-economic status
31
Q

protective factors against cervical cancer

A
  • Use of barrier contraception and spermicides
  • High levels of vitamin C
32
Q

Screening tools for cervical cancer

A
  • Pap smear
  • Colposcopy
  • HPV testing
33
Q

effectiveness of early detection of HPV

A
  • May prevent or delay progression to invasive cancer
  • Lowers incidence of invasive cervical cancer by 91%
  • Lowers mortality from cervical cancer 20% - 60%
34
Q

Cervical cancer diagnosis

A
  • Diagnosis made by histology/biopsy
  • Pelvic lymphadenectomy required for staging
  • Treatment of early stage (localized to uterus) includes hysterectomy, radiation w/wo chemo; fertility sparing surgery may be done with conization or removal of cervix only
  • Treatment of invasive cervical cancer includes chemoradiation followed by surgery