Disorders of the cervix Flashcards

1
Q

Are disorders of the cervix usually sx or asx? Early detection helps prevent what?

A
  • asx
  • early detection of abnormal cell changes and presence of HPV leads to tx that prevents the progression to cervical cancer
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2
Q

Why is the SCJ so impt?

A
  • this is where cancer is most likely to arise
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3
Q

What cells are affected in cervicitis? Etiologies?

A
  • primarily affects columnar epithelial cells
  • can cause visible changes of ectocervix
etiologies:
often caused by STIs - often asx
local trauma
malignancy, radiation therapy, chemical irritation (changing the pH), systemic inflammatory disease (Behcet's syndrome) 
idiopathic
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4
Q

What is impt about sexual activity to ask in hx?

A
  • number of partners
  • use of condoms
  • hx of STIs (women under 25 - 1/3 have chlamydia)
  • use of pessiary, diaphragm, douches
  • specific sxs (post-coital bleeding, deep pain, spotting)
  • constitutional sxs (fever, malaise)
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5
Q

Sxs of cervicitis?

A
  • purulent or mucopurulent d/c from vagina
  • intermenstrual or postcoital bleeding
  • dysuria or urinary frequency
  • dysparuenia
  • vulvovaginal irritation
  • pain and fever are atypical in the absence of upper tract infection
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6
Q

PE appearance of cervicitis?

A
  • purulent d/c on surface and/or exuding from the canal
  • minor trauma from insertion from a cotton swab - bleeding (friability)
  • diffuse vesicular lesions suggest HSV
  • punctate hemorrhages consistent with trichomonas infection
  • cervical motion tenderness is sign of coexisting PID
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7
Q

Tx fo GC and Chlamydia?

A
  • Rocephin IM and Azithro PO

- test for other STIs and HIV

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8
Q

What is pathognomic for trichomonas infection?

A
  • strawberry cervix (rare)
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9
Q

Diff b/t primary and secondary outbreaks of genital herpes?

A
  • primary: much more severe, more vesicles
  • recurrence: won’t be as severe
  • if you want - can test for abs (will have if recurrent)
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10
Q

Dx of cervicitis?

A
  • from exam and determination of risk - also test for gonorrhea, chlamydia, HSV if indicated
  • tx empirically to cover gonorrhea, chlamydia, and trichomonas:
    ceftriaxone, doxy, and flagyl
  • all pts eval for STIs should be offered counseling and testing for HIV
  • if exam shows minor erythema and low risk person, or cultures are negative then other etiologies might be in play - then there may be an offending agent that needs to be stopped
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11
Q

Tx of cervicitis?

A

persistent disease:

  • if persists after initial round of abx then repeat testing w/ most sensitive dx tests
  • re-examine possible exposure to chemical irritatants
  • have sex partner(s) be examined and tested for STIss
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12
Q

What are cervical polyps? Result of? May be assoc with? Most common in?

A
  • benign, pedunculated growths of varying size that extend from the ectocervix of endocervical canal
  • may occur singularly or may be multiple
  • etiology is unknown
  • believed to result from chronic inflammation
  • may be assoc with hyperestrogen states
  • found commonly with endometrial hyperplasia
  • MC among multiparous women in their 30s and 40s
  • MC benign neoplastic growth of the cervix
  • occurs in 4% of all gyn pts
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13
Q

When do cervical polyps commonly occur? How common are malignant changes?

A
  • commonly occur during reproductive years
  • usually arise from endocervical canal
  • etiology is unkown
  • malignant change is rare-about 1% will show neoplastic changes
  • removed fairly esaily
  • always send to path
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14
Q

Sxs of cervical polyps?

A
  • usually asx
  • thick leukorrhea
  • postcoital bleeding
  • intermenstrual bleeding
  • menorrhagia
  • post-menopausal bleeding
  • mucopurulent or blood tinged vaginal d/c
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15
Q

PE of cervical polyps?

A
  • single or multiple pear shaped growths may protrude from the cervix into the vaginal canal
  • usually smooth, soft, reddish purple to cherry red
  • may readily bleed when touched
  • may be small or very large
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16
Q

DDx for cervical polyps?

A
  • endometrial polyps
  • small prolapsed myomas
  • cervical malignancy
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17
Q

Tx of cervical polyps?

A
  • tie off base
  • twist off at base with forceps
  • may need to cauterize site
  • recurrence low
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18
Q

What are nabothian cysts?

A
  • mucous filled cyst on surface of the cervix
  • most often caused when stratified squamous epithelium of ectocervix grows over the simple columnar epithelium of endocervix
  • tissue growth can block the cervical crypts and trap mucous inside the crypts
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19
Q

How do nabothian cysts appear? Are they worrisome?

A
  • appear as firm bumps on the surface
  • considered harmless and usually resolve on their own
  • appearance may be related to menses
  • not considered problematic unless they grow really large and present secondary sxs
  • may be removed by electrocautery or cryotherapy
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20
Q

How common is Cervical cancer? Is it increasing or decreasing?

A
  • 3rd most common gyn malignancy and COD in women in US
  • in past 45 yrs its incidence has decreased from 45 to 15/100,000 women due to screening from pap smears
  • in US represents 1.3% of cancer deaths in women and in developed countries 75% decrease in incidence and mortality over 50 yrs
  • in developing countries 2nd MC cause of cancer related morbidity and mortality among women
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21
Q

Pathology of cervical cancer?

A
  • squamous cell (69%)
  • adenocarcinoma (25%)
  • adenosquamous, rare types (sarcomas) (6%)
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22
Q

Sxs of cervical cancer?

A
  • frequently asx
  • abnormal vaginal bleeding
  • postcoital spotting
  • vaginal d/c - can be watery, mucoid or purulent and malodorous
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23
Q

RFs for cervical cancer?

A
  • early onset of intercourse (b/f 18)
  • 3 or more sexual partners
  • male partner who has had other partners or is uncircumcised
  • hx of STIs (chlamydia, herpes)
  • first child prior to age 20 and multiparity (more than 3 term pregnancies)
  • cigarette smoking (SCC)
  • immunosuppression
  • OCP - especially long term
  • low socioeconomic status (not getting screened)
  • daughter of a mother who took DES
  • HPV exposure
24
Q

Why are the effects of race and social economic status controversial?

A
  • higher rates among black and especially foreign born hispanic women
  • higher rates among women of lower social economic status
  • unclear whether related to access to pap smears and other medical care or other undetected confounding variables
25
Q

Protective factors for cervical cancer?

A
  • virginity
  • long term celibacy
  • life long mutual monogamy
  • long term use of condoms
  • obtaining regular pap smears
26
Q

What is the role of HPV in cervical cancer?

A
  • at least 80% of sexually active women will have acquired a genital HPV infection by 50

most HPV infections are transient but:

  • over 50% are cleared in 6-18 months
  • 80-90% will have resolved w/in 2-5 yrs
  • HPV can be detected in 99.7% of cervical CAs
  • generally HPV alone can’t cause cervical cancer - it usually takes about 15 yrs from time of infection to presentation of cervical cancer
27
Q

Neoplastic transformation from HPV? Major factors assoc with development of HGL and cervical cancer?

A
  • HPV integrates into human genome and can result in abnormal high grade lesions and cancer
  • major factors assoc with development of HGL and cervical cancer are:
    HPV subtype: 18 and 16 (bulk of cervical cancers)
    persistence: age, duration, oncogenic subtypes
    enviro factors: cigarette smoking, infection with HIV, gonorrhea and chlamydia, HSV and OCPs
28
Q

Pathogenesis of cervical cancer - early on?

A
  • earliest SCC is confined to epithelial layers:
    intraepithelial neoplasia
    preinvasive carcinoma (carcinoma in situ)
  • the disease remains confined to mucous membrane for several years b/f invading the subjacent stroma
  • CIS occurs most frequently in 40s
  • invasive carcinoma is encountered most often in women b/t 40-50
29
Q

Pathogenesis of HPV infection to cancer?

A
  • oncogenic HPV infection at transformation zone (SJC)
  • persistence of infection
  • progression of a clone of epithelial cells from persistent viral infection to precancerous cells
  • development of carcinoma and invasion through the basement membrane
30
Q

Dx genital HPV?

A
  • pap smears prepared from cervical or anal scrapings often show cytologic evidence of HPV infection
  • persistent or atypical lesions should be bx and examined by routine histologic methods
  • the most sensitive and specific methods of virology dx - use techniques such as PCR or hybrid capture assay to detect HPV nucleic acids and to ID specific virus types
31
Q

How can we prevent HPV?

A
  • vaccinate!
  • recently developed vaccines dramatically reduce rates of infection and disease produced by HPV types in vaccines
  • gardisil:
    recommended by CDC for girls and boys 11-26
32
Q

Administration of gardisil?

A
  • admin in 3 separate intramuscular injections in deltoid region of upper arm or in higher anterolateral area of thigh
  • over a 6 mo period with first dose at elected date
  • 2nd dose 2 mo after 1st
  • 3rd dose 6 months after first
  • $180 for dose of gardisil 9
33
Q

Comfort of pt - positioning?

A
  • privacy
  • have buttocks just off table
  • good lighting
  • drape
  • assistant/chaperone
34
Q

Inserting speculum for pelvic exam?

A
  • spread labia
  • keep labia apart
  • alternate method -
    insert 2 fingers in base of vagina - then press down and insert speculum over tops of fingers
  • blades remain closed until fully inserted
  • squeeze handle to open speculum and visualize cervix
35
Q

What is the squamo-columnar jxn?

A
  • jxn of pink cervical skin and red endocervical canal
  • inherently unstable
  • key portion of cervix to sample
  • most likely site of dysplasia
36
Q

How do you sample cervix when doing a pap smear?

A
  • use concave end
  • rotate 360 degrees
  • don’t use too much force (bleeding, pain)
  • don’t use too little force (inadequate sample)
37
Q

What is the definition of a satisfactory pap?

A
  • proper amt of squamous cells
  • proper labeling
  • endocervical cells present

not satisfactory if:
scant cellularity
not properly labeled
cells obscured by blood or inflammation (menses could ruin pap)

38
Q

Normal results for a pap smear?

A
  • if no abnormal cells are seen, the test is normal

- if only benign changes are seen, usually resulting from inflammation or irritation, then the test result is normal

39
Q

Abnormal results for a pap smear?

A
  • atypical cells of undetermined significance (ASCUS, AGUS)
  • low grade squamous intraepithelial lesions or cervical intraepithelial neoplasia (CIN) 1. these are mild, subtle cell change, and most go away w/o tx
  • high grade sqaumous intraepithelial lesions (HSIL) or CIN 2 or 3. Moderate or severe cell changes which reqr further testing or tx
  • carcinoma
40
Q

Cervical intraepithelial neoplasia grades?

A
  • CIN 1 - low grade lesion: mild atypia, 1/3
  • CIN 2 - high grade lesion: moderate atypia, 2/3
  • CIN 3 - high grade lesion: severe atypia, greater than 2/3
  • incidence: high grade lesions more commonly a disease in women 25-35, while invasive cancer disease affects women over 40 more
41
Q

Natural hx of cervical cancer?

A
  • impt to manage precursor lesions
  • it is crucial to realize that not all lesions begin as condyloma (genital warts) or CIN1
  • cervical cancer may present at any pt in the spectrum depending on assoc. HPV type and other host factors
42
Q

Routes of spread of cervical cancer?

A
  • can be spread by direct extension
  • any pelvic lymph node groups may be sites of mets
  • hematogenous spread:
    lungs
    liver
    bone
43
Q

Tx of cervical cancer?

A
- according to staging system
 tx modalities:
- early stage disease: surgery or chemo
- locally advanced disease: chemo-rad
- disease with distant mets: chemo (palliative care with rad and chemo)
44
Q

What screening should be done if a pt is HIV positive?

A
  • pap smears at least annually
  • baseline colposcopic eval at time of initial dx of HIV
  • colposcopy after single reading of ASCUS or SIL Pap
  • aggressive tx of cervical disease will prolong life in most cases
45
Q

Stats of screening and cervical cancer link?

A
  • 50% of cervical cancer dx in US is found in women who haven’t been screened
  • another 10% occur in women who have not been screened for 5 yrs
46
Q

When should women start to get screened for cervical cancer?

A
  • at age 21
  • critical that adolescents who may not need yearly pap smears obtain other yearly preventative health care:
    assess. of health risks
    contraception
    prevention counseling
    screening and tx for STIs
47
Q

Why does screening not start until 21?

A
  • because there is a low risk of missing an impt cervical lesion until 3-5 yrs after initial exposure to HPV
  • earlier screening may result in over-dx of cervical lesions
  • these usually regress spontaneously but may lead to inappropriate intervention
  • young women who are infected with HIV and or immunocompromised should have pap smears twice in the first yr after dx and if normal - annual thereafter
48
Q

Screening intervals for Cervical cancer?

A
  • q 3 yrs from 21-30 a pap smear
  • for women over 30:
    q 3 yrs with a pap smear
    or
    q 5 rys with a pap smear and HPV test as long as first set were negative
  • when to stop:
    at 65
    as long as woman had 2 consecutive tests negative prior to stopping
49
Q

What should you do if you have a pt with a pap within normal limitis with a missing endocervical component?

A
  • ASCCP have published recommendations stating that a pap can be repeated in 1 yr if it was just a screening pap
  • earlier screening at 6 mo is rqd if there was a previous abnormal pap w/o 3 normal f/u paps or -
    pt is immunocompromised, pt hasn’t had regular screening, a prior pap revealed glandular abnormalities, a high risk HPV + result was obtained in past yr then it should be repeated now
50
Q

Management options if pap test result is abnormal?

A
  • for women with low grade squamous abnormalities (ASCUS or LSIL) give periodic pap tests until the abnormality resolves or colp referral for persistent lesions
  • women with glandular abnormalities (AGUS) usuall are referred for colp
  • women with HSIL are referred for colp
51
Q

HPV and the risk of CIN?

A
  • HPV is very common, occurring at least once over a 3 yr period in 60% of young women
  • lifetime cumulative risk is at least 80%
  • the longer HPV is present and the older the pt, the greater the risk of CIN
  • smoking doubles the risk of progression to CIN3 in HPV positive pts
  • the vast majority clear the virus or suppress it to levels not assoc with CIN2/3, and for most women this occurs promptly
  • duration of HPV positivity is shorter and the likelihood of clearance is higher in younger women
  • only 1/10 to 1/30 HPV infections are assoc with abnormal cervical cytology
  • the risk of cervical cancer in women who don’t harbor oncogenic HPV is extremely low
  • time coures from CIN 3 to invasive cancer averages b/t 8.1 and 12.6 yrs
52
Q

Likelihood of CIN regression to normal?

A
  • CIN 1: 60%

- CIN 2: 40%

53
Q

Type of testing done for cervical cancer?

A
  • cytology alone has low sensitivity
  • cytology + HPV testing much higher sensitivity
  • HPV testing especially helpful in pts over 30
  • if combined testing is normal, repeat combined testing only q 3 yrs
  • if pap normal and HPV positive repeat pap and HPV testing in 12 months then colp if either is +
54
Q

What is a colposcopy?

A
  • examining the cervix with a colposcope
  • application of 3-5% acetic acid soon
  • obtain colposcopically directed bx of all lesions suspected of representing neoplasia
  • do endocervical curettage
  • need to visualize all of SCJ
  • up to 10% of lesions more severe than anticipated
55
Q

Is excision or ablation better?

A
  • laser, LEEP, and cryotherapy are all ablation techniques
  • must perform endocervical sampling if ablation is planned
  • don’t perform ablation if dysplasia on endocervical curettage
  • then cold knife conization is preferred or LEEP
56
Q

Care and F/U during and after pregnancy?

A
  • only the dx of invasive cancer alters management
  • colp should have as its primary goal the exclusion of invasive cancer

higher grade test results:

  • colp w/o endocervical sampling
  • bx only if colposcopic appearance consistent w/ CIN2, AIS, or cancer
  • repeat colp each trimester w/ bx only if progression of disease is suggested or cytology is suggestive of invasive cancer