cervical screening
Rehmus, W. E. (2023). Erysipelas. Merck Manual for the Professional. Retrieved November 19, 2023, from https://www.merckmanuals.com/professional/dermatologic-disorders/bacterial-skin-infections/erysipelas
pap
CELLS SCRAPED FROM CERVIX
EXAMINED UNDER MICROSCOPE
LOOK FOR HPV NUMBER ONE CAUSE OF CERVICAL CA
PAP SMEAR AND HPV GUIDELINES
PAPANICOLAOU CAN TEST FOR HPV AND TRICHOMONIASIS
WOMEN 21-29
PAP EVERY 3 YEARS
HPV TESTING NOT RECOMMENDED
WOMEN 30-65 YEARS
PAP TEST ONLY - NORMAL =3 YEARS
HPV NORMAL =5 YEARS
HPV + PAP ( PREFERRED) NORMAL =5 YEARS ODGERS SLIDES
PAPANICOLAOU TEST
PAP
ETIOLOGY /INCIDENCE
CERVICAL CANCER SCREENING DECREASED CERVICAL CANCER BY 70%
EXFOLIATED CERVICAL CELLS FOR CYTOLOGIC STAINING AND EXAM
2.1% REVEAL CYTOLOGIC ABNORMALITIES
MAJORITY OF WOMEN W CERVICAL CANCER DID NOT HAVE PAP OR DID NOT HAVE IN LAST 5 YEARS
HPV TYPES 16 AND 18 CAUSE 70% OF ALL CERVICAL CANCERS
HPV 6 AND HPV 11 CUASE GENITAL WARTS
MOST COMMON STI
DO NOT NEED PENETRATIVE INTERCOURSE , CAN BE TRANSMITTED THROUGH DIRECT SKIN AND MUCOUS MEMBRANES TO PARTNER
ONLY A SMALL PROPORTION OF WOMEN WITH HPV PROGRESS TO CERVICAL CANCER
NOT PRESENCE BUT PERSISTENCE OF HPV INFECTION IS THOUGHT TO LEAD TO CANCER
PAP COLLECTION
NOT DURING MENSES
NOT WITHN24-48 HOURS OF SEX
NOT WHEN TOPICAL VAGINAL MEDS USED
OBTAIN FROM THE TRANSFORMATION ZONE OF THE CERVIX
XTERNAL CERVIX (ECTOCERVIX) IS STRATIFIED SQUAMOUS EPITHELIUM
INTERNAL ( ENDOCERVIX) IS MUCUS SECRETING COLUMNAR EPITHELIUM
METAPLASIA -NORMAL CELL METAMORPHOSIS FROM COLUMNAR TO SQUAMOUS - IS THE SQUAMOCOLUMNAR JUNCTION-THIS IS TRANSFORMATION ZONE -THIS IS WHERE YOU TAKE THE SAMPLE FROM
. Cervical neoplasias most often occur at the squamocolumnar junction (SCJ) and affect squamous epithelial cells (80-90% of cervical cancers)
PAP IS SCREENING TEST
BIOPSY IS DIAGNOSTIC TEST
CERVICAL SCREENING ABNORMALITIES
BETHESDA CLASSIFICATION
TWO SYSTEMS
LOW GRADE-SQUAMOUS INTRA EPITHELIAL LESION( LSIL)
AND HIGH GRADE (HSIL)
NOTE: HSIL IS A PRECURSOR LESION THAT HAS THE POTENTIAL TO DEVELOP SQUAMOUS CA
PRECANCEROUS STATE IS CALLED CIN cervical intraepithelial neoplasia
CERVICAL CA
ASST FINDINGS
ASYMPTOMATIC EARLY STAGES
ABNORMAL VAGINAL BLEEDING 80-90%
WATERRY PURULENT MALODOROUS VAGINA DISCHARGE
DYSPAREUNIA
POSTCOITAL BLEEDING
BLADDER OUTLET OBSTRUCTION
PELVIC BACK ABDOMINAL PAIN ( TUMOR INVASION)
SWELLING OF LEGS 2/2 OBSTRUCTION LYMPHATIC OR VASCULAR
CONSTIPATION
DIFF DX
SEVERE CERVICITIS
POLYP OR NABOTHIAN CYST
ENDOMETRIAL CA
VAGINITIS
PID
ENDOMETRIOSIS
CERVICAL ECTROPION
DIAGNOSTIC STUDIES
PAP TEST W HPV W TRANSORMATION ZONE COMPONENT FOUND
HPV TESTING >5
STD TESTING WET MOUNT
COLPOSCOPY W ENDOCERVICAL CURETTAGE(ecc)
LOOP ELECTROSURGICAL EXCISION PROCEDURE
COLD KNIFE CONE BIOPSY
ENDOMETRIAL BIOPSY >34 YO
CBC
CHEM
RENAL AND HEPTIC FUNCTION TESTS
MRI, CT CXR PET
NON PHARM
CIN 1 AND CIN 2 COLPSOCPY AND CLOSE OBSERVATION UNTIL RESULTS NORMAL
EXPEDITED SURGICAL RX FOR HSIL -EXCISION OVER ABLATION
REFERRALS
Gynecologist
Surgical oncologist
Gynecologic oncologist
Radiation oncologist
Radiologist
Pelvic floor physical therapist
Psychologists, social workers
HPV VACCINE
GARDASIL 9
PROTECTS AGAINST OROPHARYNGEAL AND RECTAL CANCERS FROM HPV
PRE TEEN VACCINE, 11-12 YEARS
TEENS -> 26 YEARS WHO DIDNT START OR FINISH VACCINE SHOULD HAVE VACCINATION
GUIDELINES:
11-12 YO TWO DOSES HPV V 6 -12 MONTHS APART
9-14 YO TWO DOSES
15-26 3 DOSES
9-14 <5 MONTHS APART 3RD DOSE
9-26 WEAK IMMUNE - 3 DOSES
2018 FDA
MALE AND FEMALE UP TO 45 CAN GET VACCINE, COVERS ALL NINE TYPES
LIKELY TO HAVE BEEN EXPOSED TO SOME STRAINS BUT NOT ALL
VACCINE DOES NOT TREAT EXISTING DISEASE
SCREENING CONTINUES EVEN IF VACCINATED
GENITAL WARTS CONDYLOMA
MAY NEED:
BIOPSY R/O DYSPLASIA /CA
TEST FOR OTHER STI
TREATMENT
PODOFILOX GEL 0.5 %
TRICHLOROACETIC ACID TCA BCA
CRYOTHERAPY OR SURGICAL EXCISION
MENOPAUSE
avERage age 51 in us (45-55)
1 YEAR NO PERIOD
AGE OF ONSET FACTORS
NATURAL DECREASE IN HORMONES
CHEMO/RADX
PRIMARY OVARIAN INSUFFICIENCY (POI)
HYSTERECTOMY
SYMPTOMS
SLEEP DISTURBANCE EARLY M. 32-40%
LATE M 38-46
DEPRESSION
>2.5X
ANXIETY
VAGINAL DRYNESS
ATROPHIC VAGINA
SEXUAL DYSF
HEADACHE /FATIGUE
HAIR LOSS
DRY EYES
GINGIVAL THINNING
BONE AND JOINT PAIN
SKIN THINNING
TYPES OF MENOPAUSE
SPONTANEOUS
NATURAL
OVARIAN FOLLICULAR FUNCTION ENDS
PERIMEN
TRANSITIONAL PERIOD TO MENOPAUSE
CAN BE MANY YEARS: IRREGULAR PERIODS, NIGHT SWEATS, SHORTER PERIODS
PREMATURE
GENETIC AUTOIMMUNE METABOLIC
AGE 40 OR YOUNGER
POI
<AGE 40
ABSENT SKIPPED INCONSISTENT PERIODS
PREGNANCY
THYROID DEFICIENCY
HYPOTHALAMIC DYSFUNCTION
HYPERPARATHYROIDISM
PITUITARY ADENOMA
PCOS
DM
DIAGNOSIS
DETAILED HISTORY
MENSTRUAL CALENDAR
SYMPTOMS HOT FLASH DRYNESS ETC
SEX HISTORY OF DYSPAREUNIA, REDUCED LIBIDO
VAGINAL EXAM FOR ATROPHY DRYNESS
LABS
VARIES BY AGE AND PRESENTATION
PREGNANCY TEST
FSH
PROLACTIN
TSH
DIAGNOSTICS EXPLAINED
LH-LUTEINIZING HORMONE
PERIMENOPAUSE
ESTROGEN NORMAL FSH GETS HIGHER
MENOPAUSE < ESTROGEN> FSH >LH
NO PERIOD FOR YEAR AND FSH > 30 = MENOPAUSE DX( ALTHOUGH HISTORY SUFFICES AS DX)
FSH >30 PERIMENPAUSE
FSH >70-90 COMMON POST MENOPAUSAL
>45 YO NO LABS NEEDED
40-45 LABS TO EXCLUDE OTHER DX
PREGNANCY, PROLACTIN. TSH
<40 ??POI
PREGNANCY , PROLACTION,TSH FURTHER TESTING
MENOPAUSE RX
HRT
UTERUS + ESTROGEN AND PROGESTERONE OR > RISK UTERINE CA
ORAL ESTROGEN
LOW COST GOOD EFFECT ON LDL HDL CHOL
> RISK THROMBOSIS STROKE > TRIGLYCERIDES, CRP < LIBIDO
TRANSDERMAL AND TOPICAL ESTROGEN
AVOID FIRST PASS SO LESS S/E LIVER TRIG, CRP LIBIDO REDUCTION, GI S/E
COSTLY PATCH SENSITIVITY, TRANSFER HORMONES
VAGINAL ESTROGEN
VAGINAL BENEFIT ONLY
PROGESTERONE
RELAXES HELPS SLEEP
INCREASE BREAST CA RISK - CHECK LATEST ACOG GUIDELINES ON THIS
BLOATING DYSPHORIA CAN OCCUR
HRT CONTRAINDICATIONS
PORPHYRIA CUTANEA TARDIS- ABSOLUTE CONTRAINDICATION
BREAST CA PAST OR PRESENT
ESTROGEN SENSITIVE MALIGNANCY
ENDOMETRIAL HYPERPLASIA
UNDIAGNOSED VAGINAL BLEEDING
ACTIVE LIVER DX
UNTREATED HTN
VENOUS/ARTERIAL THROMBOEMBOLISM.
PHARMACOLOGICAL NON HRT
FDA APPROVED
SSRI PAROXETINE 7.5MG
OFF LABEL
SSRI SNRI
GABAPENTIN NIGHTLY TO 4 X DAY
CLONIDINE FOR HOT FLASHES 0.005MG OD S/E PROFILE NOT GOOD
VITS AND MINERALS
IRON
CALCIUM
VIT D
MENOPAUSE NON PHARM
HOT FLASH
NO SPICY HOT CAFFEINE DRINKS
WICKING CLOTHING
LOW FAT HIGH CALCIUM DIET
BED FAN
ANX AND DEP
YOGA
MEDITATION
BIOFEEDBACK
CBT ACUPUNCTURE REFLEXOLOGY
VAGINA
KEGELS
WEIGHT AND EXERCISE
RED FLAGS
FOLLOW UP
F/U AND EDUCATION
1-2 MONTHS AFTER DRUG THERAPY FOR EFFECTIVENESS
EDUCATION-LIGHT SPOTTING NORMAL
CONTINUE WITH NORMAL SCREENINGS
POST MENOPAUSE BLEEDING - UTERINE LINING ABNORMALITIES OR CA
VULVAR PRURITUS
INCIDENCEETIOLOGY
EXAM
CHIEF COMPLAINT FOR MOST VULVAL DISORDERS
OFTEN MISDIAGNOSED OR PT NOT EXAMINED
COMMON CAUSES
STI
NEOPLASM
BARTHOLIN DUCT CYSTS
CANDIDA(ME)
OTHER CONDITIONS
TB
VULVAR PSORIASIS-UNUSUAL PRESENTATIONS-LOOK FOR NORMAL PRESENTATION ELSEWHERE ON BODY
CROHNS
IMPORTANCE OF FULL VAGINAL EXAM, MAGNIFYING GLASS OR COLPOSCOPE MAY BE NEEDED
LICHEN SCLEROSUS
INCIDENCE /ETIOLOGY
AUTOIMMUNE WEAK LINK ASSOC W DM TYPE 1 VITILIGO PERNICIOUS ANEMIA,ALOPECIA AREATA,THYROID DX
WOMEN : MEN 10:1
MENOPAUSEAL
AND PRE PUBERTY GIRLS-ESTROGEN RELATED THEORY NOT PROVEN
CLINICAL PRESENTATION
SEVERE VULVAR PRURITUS
KEYHOLE EFFECT/FIGURE 8 APPERANCE
NARROWED INTROITUS
OBLITERATION OF LABIA MINORA
WHITE PAPULES
THN WHITE EPITHELIUM-PARCHMENT
CAN RESEMBLE HYPERPLASIA
FISSURES AND TELANGIECTASIA CAN OCCUR
LS DIAGNOSTIC TESTING
THROUGH HISTORY
TIMING ONSET LOCATION AND DURATION
ALLEVIATING/AGGRAVATING
PHYSICAL EXAM WITH MAGNIFYING GLASS OR COLPOSCOPE
PUNCH BIOPSY FOR DIAGNOSIS AND RR/O ATYPIA
(PUNCH BIOPSY FINDINGS:
HYPERKERATOSIS
EPITHELIAL THINNING
CYTOPLASMIC VACUOLATION OF BASAL LAYER CELLS
FOLLICULAR PLUGGINGHOMOGENOUS SUBEPITHELIAL LAYER
INFLAMMATORY CELL INFILTRATION W LYMPHOCYTESAND FEW PLASMAN CELLS)
CBC- F INFECTION SUSPECTED
THYROID FUNCTION TESTS
ANA
B12 LEVEL ( PERNICIOUS ANEMIA)-AUTOIMMUNE TESTING MAY NOTT BE DONE AS WEAK LINK
LS
DIFF DIAG
LICHEN PLANUS
ATROPHIC VAGINITIS
CONTACT/ALLERGIC DERMATITIS
FUNGAL INFECTION
VITILIGO
TREATMENT AND REFERRAL
ULTRA POTENT CORTICOSTEROIDS 4-6 WEEKS
CLOBETASOL
HALOBETASOL
BETAMETHASONE DIPROPIONATE AUGMENTED 0.05% OINTMENT
THIN LAYER 1-2 X DAILY 2-4 WEEKS THEN 3 X WEEK FOR MAINATENANCE
INTERESTING THAT VULVA IS NOT SUSCEPTIBLE TO LONG TERM TOPICAL CCS ATROPHY AND SKIIN THINNING-VULVA CAN TOLERATE LONG TERM SUPERPOTENT STEROIDS
IF RECURS SWITCH TO MILDER
EG BETAMETHASONE VALEARATE 1% HIGH POTENCY
OR TRIAMCINOLONE 0.1 %
OR FLUOCINOLONE ACETONIDE 0.025% ( MODERATE POTENCY )LONG TERM MGT
ABX TOPICAL-
MILD INFECTION
TOPICAL ESTROGEN
ORAL ANTIHISTAMINE
HYDROXYZINE 25-50 MG OR BENADRYL
IMMUNOSUPPRESSANT -TOPICAL CALCINEURIN INHIBITORS, RETINOIDS- ACITRETIN
LS NON PHARM
REFERRAL
COOL COMPRESSES
COTTON CLOTHING
LOOSE FITTING CLOTHES
PUNCH BIOPSY RESULTS INDICATE HYPERPLASIA OR APLASIA ONC GYN
SURGICAL CONSULT FOR SEVERE ARCHITECTURAL CHANGES OR SCARRING
SLIGHT INCREASED CHANCE OF SQUAMOUS CELL CARCINOMA
GYN DERMATOLOGY IF NO RESPONSE TO TOPICAL STEROIDS
PT EDUCATION
LIFETIME DX
WILL GET EXCACERBATION
SEXXUALLY ACTIVE PAIN
https://www.thevpfoundation.org/
https://www.nva.org/
ETIOLOGY INCIDENCE
LICHEN PLANUS PICTURE IS EROSIVE LP
AFFECTS SKIN SCALP MUCOUS MEMBRANES OF MOUTH VAGINA AND VULVA
WOMEN
MOSTLY MIDDDLE AGED,
TCELL MEDIATED DX
LP
CLINICAL FINDINGS AND PE
CLASSIC
WLL DEFINED WHITE RETICULATED PLAQUES
EROSIVE
ERYTHEMATOUS EROSIVE LESIONS
CAN LEAD TO LEUKORRHHEA AND STENOSIS INTROITUS
MAY BE ARCHITECTURAL CHANGES
PAIN PRURITUS
BURNING DYSPAREUNIA DYSURIA
DIAGNOSTICS
THOROUGH HISTORY
PHYSICAL MAGNIFYING GLASS , COLPOSCOPY MAY BE NEEDED
BIOPSY:
FINDINGS
CHRONIC INFLAMMATION
LYMPHOCYTES W FEW PLASMA CELLLS
ACANTHOSIS AND THINNING EPITHELIUM
R/O HSV
PCR
AND BECHETS DISEASE-AUTOIMMUNE TESTING
CAN BE HARD AS CLASSIC DIFFERENT APPEARANCE TO EROSIVE
LICHENI SCLEROSUS
ULCERATIVE STI HSV OR SYPHILLIS CHANCROID
BECHETS DX
CONTACT ALLERGIC DERMATITIS
FUNGAL
EDUCATION
EXACTLY SAME AS LS
PETROLATUM BARRIER OINTMENT ADDED
OTHERWISE THE SAME
REFER TO PAIN MGT AND GYN DERM IF NO RESPONSE
OTHER VULVAL
LICHEN SIMPLEX CHRONICUS LSC
AGE >30 AND MENOPAUSE
PRURITUS IS HALLMARK SYMPTOM
LSC OR SQUAMOUS CELL HYPERPLASIA- VERY ITHCY , HISTOLOGIC ECZEMATOUS HYPERKERATOTIC,LICHENIFICATION. CHRONIC SCRATCH ITCH
RX CCS TOPICAL TOPICAL BARRIER PETROLATUM
ANTIHISTAMINES DOXEPIN BENADRYL Q NOCTE
TCA-AMITRYPTILLINE FOR ITCH
REFERRAL SAME GYN DERM
CONTACT DERMATITIS
MOIST SKIN
URINE
ERYTHEMA AND EDEMA ARE HALLMARK SIGNS
USU NOT VAGINAL DISCHARGE
RX
REMOVE ALLERGEN
CCS TOPICAL
ANTIHISTAMINE - HYDROXYZINE
SITZ BATH EMOLLIENT
BURROWS COMPRESS DOMEBORO ANTIBACTERIAL AND ANTIFUNGAL WRUNG OUT OTC SOLUTION BID
POTENTIAL VULVAR IRRITATNS
Tight clothing, spandex clothing, synthetic underwear, latex and elastic in clothing
2. Laundry detergent, fabric softener, dryer sheets, bleach
3. Rough, scented, or colored toilet paper; personal wipes
4. Menstrual hygiene and incontinence products including pads, panty liners, and tampons (especially if scented
5. Personal hygiene products including soap, shampoo, conditioner, bubble bath, and shower gel
6. Perfumes, body sprays, deodorants, douches, powders, lotions, creams, hair removal products (wax, razors, shaving cream, depilatories)
7. Urine, feces (especially if incontinent), seminal fluid, sweat
8. Commercial vaginal lubricants, condoms, spermicide
VULVAL ECZEMA AND PSORIASIS
ETIOLOGY/INCIDENCE
AND FINDINGS
PSORIASIS - LOOK FOR SYMPTMS EXTENSOR
INHERITED NEW SKIN CELLS PRODUCED TOO QUICKLY RED AND SCALY OR SILVER WHITE
NEW PSORIASIS CAN DEVELOP AT AN AREA OF INJURY ( KOEBNER PHENOMENON)
AFFECTS LABIA NOT MUCUS MEMBRANES
CAN PRESENT AS SMOOTH ERYTHEMA NON SCALY INITIALLY
ECZEMA
USUALLY RESULT OF ITCHING
LOOK FOR ECZEMA ELSEWHERE
SEVERE PRUTRITUS LASTING FEW WEEKS
RED RASH ERYTHEMA INDISTINCT BORDERS
IF LEFT UNTREATED CAN LEAD TO LSC AND THICK SCALY PLAQUES SEEN IN SQUAMOUS CELL HYPERPLASIA
OCCURS ACROSS THE LIFE SPAN
SYMPPTOMS WORSE WITH LOWER ESTROGEN AND ATROPHY
VULVA ECZEMA AND PSORIASIS
DIFF DIAGNOSES
LICHEN SCLEROSIS
FUNGA’
E& P
USUA CLINICAL EXAM AND HISTORY
PUNCH DIOPSY IF OTHER THINGS RULED OUT
E&p
PHARMTREATMENT
TOPICAL AND INJECTABLE STEROIDS
SEVERE ECZEMA:
POTENT CCS CLOBETASOL 1-2 X DAY FOR 2-4 WEEKS ,TAPER TILL SYMPTOMS RESOLVE
CAN USE LOW POTENCY STEROIDS WHEN APPROPRIATE
TRIAMCINOLONE ACETONIDE INJECTIONS FOR RECALCITRANT
ORAL ANTIHISTAMINES
BENDADRYL
DOXEPIN IS H1 AND H2 RECEPTOR ANTAGONISTANTIHISTAMINE
HYDROXYZINE
DOVONEX OR CALCIPOTRIENE OINTMENT ( VITAMIN D3 PREP ) IS EFFECTIVE
E&P
NON PHARM TREATMENT
COOL COMPRESES
BURROWS SOLTUION
ULTRAVIOLET TREATMENT- QUESTIONABLE NEED LOW DOSE
LOOSE CLOTHING
AVOID HARSH CLEANSERS
COTTON
REFERRRAL'
DERM GYN PHYSICIAN
VULVAR VESTIBULITIS AND ESSENTIAL VULVODYNIA
VVS
CHRONIC INFLAMMATORY CONDITION
REPRODUCTIVE AGE AND SEXUALLY ACTIVE
8-16% WOMEN UNDER 40
PRIMARY -ONSET AFTER 1STT INTERCOURS OR TAMPON
2NDRY VAGINITIS TREATMENT, POSTPARTUM, HPV
PAIN IN VESTIBULE
EV
VULVAL BURNING AND PAIN, NOT LIMITED TO VESTIBULE
CAN BE NEUROPATHIC -PUDENDAL NEURALGIA , REFLEX SYMPATHETIC DYSTROPHY
TRIGGER EVENT
SUGGESTED FOR BOTH, VULVAR AND VAGINAL YEAST INFECTIONS FREQUENTLY TREATED,CANDIDA AUTOIMMUNE RESPONSE)
INTERSTITIAL CYSTITIS CAN BE CAUSE
ESTABLISHED THAT NOT PSYCHOGENIC
VVS AND EV
CLINICAL PRESENTATION AND PE
VVS SEVERE PAIN INTROITAL PENETRATION, VIA SEX OR TAMPON, BICYCLE OR HORSEBACK TIGHT CLOTHES
PAIN SECONDS TO DAYS
HX OF FREQUENT CONSULTATIONS
IMPROTANT HISTORY
TRIGGER
IMPACT ON DAILY LIFE
BACK PAIN
BOWEL AND BLADDER FUNCTION
PRIOR VAGINOSIS , CANDIDA INFECTIONS, CYSTITIS
RECTAL PAIN
USU UNREMARKABLE FINDINGS VVS ERYTHEMA AROUND VESTIBULAR GLANDS
SALINE MOISTENED Q TIP TEST FOR SENSITIVITY TO TOUCH
TIP ON CLITORIS LABIA MINORA URETHRA VESTIBULE - BURNING TENDERNESS LEVEL OF DISCOMFORT
NO COLPOSCOPY UNLESS HPV SUSPECTED
DIAGNOSTIC TESTING VVS AND EV
INITIAL
COTTON SWAB TEST
LAB
GONORRHEA
CHLAMYDIA
UREAPLASMA
B HEMOTLYIC CUTLRES
KOH FOR YEAST AND VAGINOSIS
CANDIDA
B HEMOLYTIC STREP
TREATMENT PHARM
NO STANDARD PAIN MEDS OR OPIATES- DO NOT WORK
ANTIDEORESSANT
INTERFERE WITH NEGATIVE PAIN FEEDBACK LOOP
TCA AND SSRI
NOT PRESCRIBED FOR DEPRESSION, PRESCRIBED FOR PAIN
TOPICALS
XYLOCAINE FOR PAIN DURING INTERCOURSE
ESTROGEN CREAM IF MENOPAUSAL
ANTIFUNGA
IF RECURRENT CANDIDA CAN TRY FLUCONAZOLE 150 MG WEEKLY FOR 2 MONTHS THEN BIWEEKLY FOR 2 MONTHS -CAERFUL EVAL FOR DRUG INTERACTIONS EG ORAL HYPOGLYCEMICS, ANTICOAGULANTS
NO TOPICAL ANTIFNGALS- WILL AGGRAVATE
VVS AND EV NON PHARM
PFE BID BIOFEEDBACK EXERCISES
CHRONIC PAIN MGT
GUIDED IMAGERY
ACUPPUNCTURE
PELVIC FLOOR MUSCLE CAN HAVE INCREASED TONE OR BE ASYMMETRIC IN VVVS ND EV
SEXUAL THERAPIST
MENTAL HEALTH PROVIDER
AVOID VULVAR IRRITANTS
COMMERCIAL LUBRICANTS
NORMAL MENSTRUAL CYCLE
4.5 - 8 DAYS
FREQUENCY 24-38 DAYS
IRRGULAR IS A VARIABILITY GREATER THAN 20 DAYS
NORMAL BLOOD LOSS 5-80 ML
80 MLS IS EQUIVALENT TO THREE SOAKED PADS OR SIX TAMPONS A DAY FOR 3 OR MORE DAYS
PALM-COEIN
UTERINE STRUCTURAL ABNORMALITIES
P POLYPS
A ADENOMYOSIS
L LEIOMYOMA
M MALIGANCY AND HYPERPLASIA
UTERINE NON STRUCTURAL ABNORMALITIES
C COAGULOPATHY
O OVULATORY
E ENDOMETRIAL
I IATROGENIC
N NOT OTHERWIE XLASSIFIED
DYSMENORRHEA
NSAIDS AS PROSTAGLANDIN INHIBITORS
PROSTAGLANDIN PROLONGS UTERINE CONTRACTIONS CAN BE CALLED UTERINE ANGINA AS IT CAN CUASE UTERINE ISCHEMIA
OVARIAN CANCER AND OTHER LADY CANCERS
OVARIAN
ENDOMETRIAL
UTERINE
OVARIAN:
ADNEXAL MASS
PELVIC OR ABDOMINAL SYMPTOMS
BLEEDING IS UNCOMMON
ENDOMETRIAL CANCER
AVERAGE AGE IS 60 YO
ADENOCARCINOMAS
TYPE 1
ESTROGEN EXCESS
NO PROGESTERONE TOS USTAIN VASCULARITY OF THICK ENDOMETRIAL WALL SO BLEEDS COMMON
RISK FACTORS
OBESITY-CONVERT TESTOSTERONE TO ESTROGEN
HLD
LOW PARITY
LATE MENOPAUSE
FAVORABLE PROGNOSIS
TYPE 2
NORMAL WEIGHT
POOR PROGNOSIS
CLINICAL FINDINGS
PE
DIAGNOSTIC
BLEEDING POST MENOPAUSE MOST IMPORTANT SIGN
FULLNESS /PRESSURE IN PELVIS
PAINFUL URINATION
DDYSPAREUNIA
PELVIC PAIN
POST COITAL BLEEDING
BIMANUAL PELVIC EXAM
TRANSVAGINAL USS
REFER FOR BIOPSY ENDOMETRIUM
BLEEDING IN POST MENOPAUSAL WOMEN SHOULD BE ASSUMED TO BE CANCER UNTIL PROVEN OTHERWISE
OVARIAN CANCER
5TH LEADING CAUSE OF DEATH
63 OR OLDER
WHITE
MOST COMMON TYPE IS EPITHELIAL
BRCA 1 AND BRCA 2 GENE MUTATIONS ASSOCIATED WITH OVARIAN CANCER
LYNCH SYNDROME
PEUTZ JEGHERS SYNDROME
NULLIPARITY
EARLY MENARCHE
OBESITY
HISTORY IS IMPORTANT
RED FLAG SIGNS
ABDOMINAL PAIN
URNIARY URGENCY AND FREQUENCY
INCREASED ABDOMINAL SIZE/BLOATING
EARLY SATIETY
DIFFICULTY EATING
EXAM WONT YIELD ANYTHING
IF PELVIC MASS REFER
AMENORRHEA
etiology incidence
transient or permanent
primary or secondary
PRIMARY
ABSENCE OF SPONTANEOUS UTERINE BLEED AND DELAYED PUBERTY AT AGE 14 OR BY 2 YEARS AFTER SEXUAL MATURATION,BY 16
AVERAGE RANGE 9-16 YEARS AGE 12.7
AGE OF PARENT AT MENARCHE,BODY FAT, NUTRITIONAL STATUS
SECONDARY
MORE COMMON, 1-3 %
25% FEMALE ATHLETES HAVE THE TRIAD: AMENORRHEA,OSTEOPOROSIS AND AN EATING DISORDER
PATHOPHYSIOLOGY
STRUCTURAL-OUTFLOW PROBLEMS
IMPERFORATE HYMEN, CERVICAL STENOSIS, TRANSVERSE VAGINAL SEPTA
CHROMOSOMAL WOMEN NEED TWO X CHROMOSOMES
PRESENCE OF A Y OR FRAGMENT OF Y RESULTS IN GONADAL FAILURE OF SOME TYPE
HYPOTHALAMUS
PROBLMS WI SYNTHESIS OR RELEASE OF GnRH-hypogonadism
HYPOTHALAMUS-PITUITARY-OVARIAN AXIS DISORDERS
LEPTIN PRODUCED BY ADIPOSE TISSUE MAY CONTROL SEX STEROIDS, GONADOTROPHINS ,GNRH WHEN ENERGY DEFICIENT….INTENSE EXECRICSE, EATING DISORDERS,STRAVATION, PSYCHOGENIC STRESS CAN CAUSE DEFICIENT HORMONES AT HYPOTHALAMIC LEVEL 2/2 LO LH THEREFORE LOW ESTEROGEN
ESTROGEN
LOW ESTROGEN LEVEL IN AMENORRHEA
HIGH PROLACTIN ANENORRHEA
BREAST FEEDING
PITUITARY TUMORS
RENAL FAILURE
BENZODIAZEPINES
COCAINE
AMITRYPTTILLINE
CAISES ANOVULATION DUE TO IMPAIRED GONDAOTROPHIN PULSATILITY ( LOOK IT UP) WHICH LEADS TO DERANGEMENT OF LH AND ESTROGEN
DRUGS-CHEMO, GABAPENTIN, HEROIN
AUTOIMMUNE-SLE, ADDISONS THYROID LOW OR TOXICITY
AMENNORRHEA
HISTORY
AGE AT MENARCHE
FREUQNECY
DURATION
FLOW
LMP
HISTORY OF MISSED MENSES
SEXUAL HX, LAST INTERCOURSEE, BIRTH CONTROL, PARA GRAVIDA
SX HISTORY
FAM HISTORY AGE OF MENARCHE /INFERTILITY
LOOK FOR PAST OVULATORY CYCLES: BREAST TENDERNESS, ABD PAIN, BLOATING, CHANGES IN CERVICAL MUCUS
PMH FOR DM AUTOIMMUNE, RADIATION OR CHEMO , SIGNS OF OSTEOPOROSIS,THYROID AND ADRENAL FUNCTION
EATING DISORDERS -LANUGO, THIN, LOW TEMP, LO BP , DRY SKIN CHIPMUNK CHEEKS ,CHVOSTEK SIGN -IPSILATERAL FACE TWITCH
DRUG USE ESP OTC
RECENT WEIGHT LOSS /GAIN
LOOK FOR SIGNS OF HYPERANDROGENISM ( HAIRY, TRUNCAL OBESITY, DEEP VOICE) OR GALACTORRHEA ( PITUITARY /HYPOTHALAMUS
HYPOESTROGEN ( HOT FLASHES VAG DRY DEPRESSION, DYSPAREUNIA)
LIFE STRESSORS
LOOK FOR ANDROGEN INSENSITIVITY -NO PUBIC OR AXILLA HAIR
GALACTORRHEA = HIGH PROLACTIN
AMEN
ASSESS ALLA BOVE
BODY
VAGINA EPITHELIUM AND MUCUS
AXILLAE -ACANTHOSIS NIGRICANS OR LACK OF HAIR
THYROID AND PARATHYROID , NODULES MASSES
BREASTS-GALACTORRHEA
EYES, ACUITY AND FUNDUS- RETINAL ABNORMALITITIES -MAY REFLECT IC MASS
ABDOMINAL STRIAE ON NULLIPAROUS WOMEN -HYPERCORTISOLISM
SKIN TAGS, FISSURES FOBT MAY BE IBD
EXCLUDE PREGNACY OR BREAST FEEDING
SERUM HUMAN CHORIONIC GONADOTROPIN
THYROID PROFILE
FSH , LH
FURTHER LABS
DHEA->700 mg/dL+ ADRENAL CAUSE
SERUM GLUCOSE , ELECTROLYTES BUN AND CR
ESR -AUTOIMMUNE
HGBAIC
URINARY FREE CORTISOL
IMAGING
CT OR MRI -SELLAR BODIES
OTHER DIAGNOSTICS
CLOMIPHENE CHALLENGE TEST
HYSTEROSALPINGOGRAM
ANOVULATION TESTS
ANOVULATION
CUSHINGS
ADRENAL OR OVARIAN TUMORS
PCOS -OST COMMON
FSH >20IU/L IS PCOS
FSH >30 IU/L IS MENOPAUSE
PITUITARY AND HYPOTHALAMIC -LH PLUS MRI OF SELLAR REGION-
DIFF DIAGNOSTICS
ARE ALL THE CAUSES
REFER TO APPROPRAITE SPECIALIST
SECONDARY AMENORRHEA
CAUSES
FIRST TOW YEARS OF PERIODS NORMAL
DISCONTINUATION OF ORAL CONTRACEPTIVES -RETURNS 6 MONTHS
DEPO PROVERA-RETURNS 6-14 MONTHS
PCOS HYPERANDROGENIC
OBESITY RELATED
DO HORMONE LEVELS TO RULE OUT AND IN
TSH LH FSH PROLACTIN
DEPENDS ON CAUSE
REFER
NUTRITION COUNSELLING
VITAMIN D
HOSPITALIZATION ANOREXIA NERVOSA 30% WEIGHT LOSS
ANDROGEN EXCESS >RISK CAD AND LIPID ABNORMALITIES
BREAST DISORDERS
CANCER
MOST COMMON CANCER IN WOMEN,2ND LEADING CANCER DEATH CAUSE
A WOMANS LIFETIME RISK IS 12 %,CURRENT SURVIVAL RATE 90%
OLDER AGE
FAMILY HISTORY
BRCA GENE MUTATION
BLACK WOMEN 40% MORE LIKELY TO DIE FROM BREAST CANCER THAN WHITE WOMEN
EARLY MENARCHE AND LATE MENOPAUSE
AGE 30 FIRST BIRTH SAME RISK AS NULLIPAROUS WOMEN
<30 FIRST BABY, SUBSEQUENT BABIES AND LENGTH OF BREAST FEEDING ALL REDUCE BC RISK
HRT FOR MENOPAUSE
ALCOHOL
SMOKING
RADIATION TO CHEST
USPTSF
FIRST DEGREE RELATIVE W BC =2 FOLD INCREASED RISK
TWO FIRST DEGREE RELATIVES BC= 3FOLD RISK
FIRST DEGREE RELATIVE <40YO =3FOLD RISK
PERSONAL HISTORY OF DUCTAL CARCINOMA IN SITU, INVASIVE BREAST CA OR LOBULAR CARCINOMA= VERY HIGH RISK FOR NEW-4-5 FOLD
RISK ASSESSMENT TOOL BCRISKTOOL
https://bcrisktool.cancer.gov/calculator.html
BCRF BREAST CANCER SCREENING RECOMMENDATIONS
https://www.bcrf.org/blog/uspstf-new-breast-cancer-screening-guidelines-2023/?utm_source=google&utm_medium=cpc&gclid=CjwKCAiA9ourBhAVEiwA3L5RFvC5Ied9rJs_rJCZSL93nDGpVJ91tU2wb_w6unTt2KLZ02pkHI8RDhoC_v4QAvD_BwE
USPSTF
START BREAST CANCER SCREENING AT AGE 40
EVERY OTHER YEAR MAMMOGRAMS AGE 40-74-OTHER ORGANIZATIONS -ACOG AND AMERICAN CANCER SOCIETY RECOMMEND YEARLY MAMMOGRAM
ACOG 2017
Use shared decision-making to select screening choices
Clinical breast examination may be offered every 1-3 years for women aged 29-39 years and annually for women aged ≥ 40 years
Start offering mammography at age 40 years; initiate after counseling, if patient desires
Recommend starting mammography screening by no later than age 50 years
Mammography may be annual or biennial; biennial screening is particularly reasonable after age 55 years
Continue mammography until age 75 years, then discuss discontinuation, with the woman's health status and longevity as considerations
INSURANCE IN US MUST COVER ANNUAL MAMMOGRAPHY
BREAST CANCER SCREENING ODGERS
CBE Q 3YEARS TO AGE 40
CBE ANNUALLY OVER AGE 40
MAMMOGRAPHY ANNUALLY AGE 40 OR 10 YEARS BEOFRE DIAGNOSIS IN WOMEN WITH FIRST DEGREE RELATIVE
BREAST CANCER SCREENNING DR ODGERS
PREVENTION
CBEEVERY 3 YEARS TO AGE 40 AND ANNUALLY OVER AGE 40
MAMMOGRAPHY ANNUALLY BEGINNING AT AGE 40 or 10 YEARS BEFORE AGE OF DIAGNOSIS IN FIRST DEGREE RELATIVE
TERTIARY PREVENTION
REFER TO ONC TEAM
DEPENDENT ON TUMOR STAGE, PRESENCE OF HORMONE RECEPTORS AND PT SYMPTOMS/PREFERENCES
me acog guidelines 2017
mammo 40-75 every 1-2 years. earlier if risk - gail guideline
dense breasts- acog do not need extra testing ( uss) if no risk factors
note: germline cancer risk includes breast and pancreatic
fda 2023 must notify pt that dense breast mammogram is not as sensitive to discern cancer or not
BREAST SELF EXAM GUIDELINES
SHOWN NOT TO REDUCE MORTALITY EVEN WITH APPROPRIATE TRAINING AND CAUSED UNNECESSARY BIOPSIES
ACOG REMOVED RECOMMENDATION FOR BSE AND RECOMMEND BREAST SELF AWARENESS
BSA
ATTUNEMENT TO NORMAL FEEL AND LOOK OF HER BREASTS, NOTIFY PROVIDER IF NEW PAIN, MASS , NIPPLE DISCHARGE AND REDNESS
ACOG RECOMMENDS CBE - CLINICAL BREAST EXAM ESP IN WOMEN UNDER 40 YEARS
BREAST CANCER PROTECTIVE FACTORS
ESTROGEN RECEPTOR MODULATORS(TAMOXIFEN)
AROMATASE INHIBITORS
PROPHYLACTIC MEASTECTOMY
OVARIAN ABLATION
EXERCISE
TYPES OF BREAST CANCER
estrogen-receptor negative
progesterone negative
ERBB2-negative [formerly HER2/Neu-negative]).
DIAGNOSITC BC
CBE
MAMMOGRAM 3D FEWER FALSE POSITIVES
GENETIC TESTING/COUNSELLING
FOR WOMEN WHO HAVE FAMILY MEMBERS WITH BREAST OVARIAN OR PERITONEAL CANCERS ( LOOK OUT FOR GERMLINE PANCREATIC CANCER- ASSOCI WIHT BRCA GENE)
ODGERS:
MAMMOGRAPHY
USS
REFER T BREAT SPECIALIST FOR
NEEDLE BIOPSY- EXCISIONAL BIOPSY IS MOST RELIABLE DIAGNOSTIC TEST WHERE STAGING OF TUMOR IS DONE
NIPPLE DISCHARGE AND GALACTORRHEA
20-25% WOMEN W BREAST COMPLAINTS
PHYSOIOLGIC
PATHOLOGIC
;GALACTORRHEA
COMMON IN PRE MENOPAUSAL AND PREGNANT WOMEN
USU BILATERAL
PATHOLOGIC IS SPONTANEOUS BLOODY SEROUS ONE DUCT 1/3 CANCER
GALACTORRHEA = PITUITARY ADENOMA OR HYPOTHYROIDISM
OTHER S/S LETHARGY COLD INTOLERANCE, DRY SKIN ,AMENORRUEA
PROLACTIN LEVEL AND BRAIN MRI
PHYSIOLOGIC
BILATERAL, MULTIPLE DUCTS,EXPRESSION NOT SPONTANEOUS -CLEAR YELLOW DARK GREEN COLOR
HORMONE RELATED , GROWTH,ADRENAL , INSULIN
COMMONEST CUASE INTRADUCTAL PAPILLOMA
IF MASS PRESENT ALSO , > RISK CANCER
PE NIPPLE DISCHARGE
THOROUGH BREAST EXAM
COMPRESS AREOLA BETWEEN FINGER AND THUMB TO MILK DUCTS -IS IT ONE OR A FEW?
FUNDOSCOPY IF GALACTORRHEA ( RETINAL ABNORMAL IC MASS)
EOM VISUAL ACUITYVISUAL FIELDS - COMMON IN PARAPITUITARY LESIONS
NEUROLOGIC EXAM
THYROID EXAM
FULL PMH
ENDOCRINE AND REPRODUCTIVE HISTORY
NIPLE DISCHARGE
DISCHARGE FOR OB IF SEROUS OR WATERY
NO CYTOLOGY ( DOESNT RULE OUT MALIGNANCY)
MAMMOGRAM
USS PREIAREOLAR
SERUM PROLACTIN ( PITUITARY OR CNS ORIGIN)
MRO BRAIN IF SYMPTOMS OF IC MASS
GALACTORRHEA WITH AMENORRHEA
OR ELEVATED PROLACTIN LEVEL
NIPPLE DISCHARGE
IF NOT SIGNS OF CANCER
DUCT ECTASIA
NON PUERPERAL MASTITITIS
INTRADUCTAL PAPILLOMA
BREAST CA
TREATMENTNIPPLE DISCHARGE
TREAT UNDERLYING CAUSE
IF DUCT ECTASIA IT IS BENIGN, NO TREATMENT
IF RECURRENT BREAST SURGEON
IF INTRADUCTAL PAPILLOMA BREAST SURGEON
PAGETS DISEASE OF THE NIPPLE
TREATMENT PUNCH BIOPSY AS OFFICE PROCEDURE OR REFER TO DERM OR SURGEON
PAGETS VERSUS ECZEMA
INTERMITTENT HX WITH RAPID PROGRESSION
MOIST INITIALLY
INDISTINCT BORDER
AREOLA INVOLVED NIPPLE MAY BE SPARED
ITCHING COMMON
PAGETS
UNILATERAL
CONTINUOUS HX WITH SLOW PROGRESSION
MOIST OR DRY
IRREGULAR BUT DISTINCT BORDER
NIPPLE ALWAYS INVOLVED AND DISAPPEARS IN ADVANCED STAGE
BREAST MASSES
ETIOLOGY
UP TO 85% WOMEN WITH NO HISTORY WILL DEVELOP BREAST CANCER
90% BREAST MASSES ARE BENIGN CYSTS FIBROADENOMAS FIBROCYSTIC CHANGES-PREMENOPAUSAL
DIFFERENT <30 FIBROCYSTIC CHANGES BENIGN
31-50 YO USU CYSTS - BENIGN FLUID FILLED
AND >50 YO
FIBROADENOMAS PAINLESS WELL CIRCUMSCRIBED FREELY MOVABLE MASSES ROUND OR LOBULAR , RUBBERY , MAY BE HARD CALCIFIED, HORMONALLY RESPONSIVE -MOST COMMON IN 20S AND 30S-BENIGN
BENIGN PHYLLODES - RAPIDLY GROWING BREAST MASS,
FOCAL AREAS OFTEN BIOPSIED AND ARE BENIGN STROMAL FIBROSIS
DUCTAL CARCINOMA NOT USU FOUND AS A LUMP BUT DETECTED ON MAMMOGRAM AS ABNORMALITY SUCH AS CALCIFICATION
GALACTOCELE-MILK CYST IN PREGNANT WOMEN
PEE
HISTORY DURATION
PAIN
ASSOC SKIN CHANGES
PRESENCE OF AXILLARY, SUPRA OR INFRACLAVICULAR ADENOPATHY
CHANGE IN SIZE OR TEXTURE OVER TIME
RELATIONSHIP TO MENSTRUAL CYCLE
RECORD
SIZE
LOCATION
SHAPE
MOBILITY
LYMPH NODES
DISCHARGE
CBE IS NOT AN INDEPENDENT DIAGNOSTIC TEST
MAMMOGRAPHY + USS IF >25 YO
USS <25 YO
15-18% MAMMOGRAMS APPEAR NEGATIVE IN PRESENCEE OF PALPABLE CANCER
ADDITIONAL BIOPSY
DISCRETE MASS ALWAYS REQUIRES SURGICAL REFERRAL FOR BIOPSY
NEEDLE BIOPSY -EXCISIONAL BIOPSY IF MOST RELIABLE DIAGNOSTIC TEST
CYST CAN BE ASPIRATED FOR RELIEF OF PAIN AND CYTOLOGY-4-6 WEEK FOLLOW UP FOR RECURRENCE OF CYST
ANY DISCRETE SOLID MASS REQUIRES TISSUE BIOPSY R/O CANCER
SOLID MASS
NSTDC
HPV
SMALL DOUBLE STRANDED DNA THAT CAN BE ONCOGENIC
MOST HAVE NO CONSEQUENCES
UROGENITAL
CERVICAL FOR WOMEN
OROPHARYNGEAL FOR MEN
6 AND 11 CAUSE ANOGENITAL WARTS
INCIDENCE & PREVALENCE
CERVICAL WARTS
INCIDENCE
MOST SEXUALLY ACTIVE MEDN AND WOMEN WILL ACQUIRE HPV INFECTION
90% WILL RESOLVE SPONTANEOUSLY WITHIN 2 YEARS + CLINICALLY SILENT
CDC
13 MILLION NEW HPV CASES IN 2018, ONLY 12% IN MSW, 41% WOMEN
ANOGENITAL WARTS INCUBATION 3-6 (wOMEN) -11 MONTHS(MEN) BEFORE SEEN
OROPHARYNGEAL CANCER
CERVICAL CANCER PRE CANCER OCCURS YEARS AFTER AND CANCER OCCURS DECADES AFTER INITIAL INFECTION
ANAL CANCER
PRECANCERS CAN REGRESS AND PROGRESS
SEXUAL PARTNER NUMBER,
EARLY AGE OF SEXUAL DEBUT
ORAL SEX
IMMUNOSUPPRESSION
LONG TERM ORAL CONTRACEPTIVE USE
TOBACCO SMOKING
COINFECTION WITH HIV, CT HSV 2
DNA SELF REPAIR CONSTANT, REPLICATE FROM TEMPLATE STRAND IS ONE METHOD
CELL MEIOSIS AND MITOSIS
PATHOGENESIS AND MICROBIOLOGY
SMALL NON ENVELOPED DOUBLE STRANDED DNA VIRUS, CREATES A SHELL THAT LINKS TO THE HPV DNA
HPV IDENTIFIED BY DETECTION OF HPV DNA OR HPV mRNA
MORE THAN 70 TYPES IN HUMAN GENITAL TRACT-HAVE AN AFFINITY FOR THIS TRACT
INFECTION AT BASAL LAYER OF STRATIFIED SQUAMOUS EPITHELIAL CELLS
LOW RISK
HPV 6 AND HPV 11( NONONCOGENIC) CAUSE 90-95% ANOGENITAL WARTS
HIGH RISK
CAUSE LOW GRADE + HIGH GRADE CERVICAL CELLULAR CHANGES ,SOME HIGH RISK TYPES CAUSE CULVA VAGINA ANAL PENIS AND OROPHARYNX CANCERS
TWELVE TYPES
16-18-31-33-35-39-45-51-52-56-58-59
65-705 CAUSED Y 16 + 18
TRANSMISSION FROM FRICTION INDUCED MICROABRASIONS IN SKIN TO SKIN
NSTDC HPV
VISIBLE ANOGENTIAL WARTS USU MULTIPLE HPV TYPES
CANB EC ONFUSED
CONDYLOMATA LATA-SECONDARY SYPHILLIS
MOLLUSCUM CONTAGIOSUM
HERPES VEGETANS
SQUAMOUS CELL CA
VESTIBULAR PAPILLAE
SKIN TAGS
BOWENS DISEASE
NEOPLASMS
HSV CONDYLOMA ACUMINATA-CAULIFLOWER
SMOOTH PAPULES DOME SHAPED
FLAT PAPULES
KERATOTIC WARTS
HPV CLINICAL FINDINGS CONTD
BLEEDING
TUMORS ULCER MASS
HPV SCREENING
ANOGENITAL WARTS
ONLY BX IF ATYPICAL-BLEEDING OR ULCERATED
IMMUNOCOMPORMOISED HOST
NOT RESPONSIVE TO THERAPY
WORSEEN DURING RX
PAP-COLLECT FROM EDOCERVIX AND ECTOCERVIX
ENDOF BROOM
ECTOSPATULA-CYTOLOGY SLIDE OR LIQUID BASED TEST
HPV SCREENING GUIDELINES 2021
PAP IS NOT AN STI SCREENING TEST
FROM 10-20 DAYS AFTER MENSES CONVENTIONAL TEST
LIQUID TEST ANYTIME DURING MENSTRUAL CYCLE
IF HAS OTHER STI S REPEAT PAP AFTER THEY ARE TREATED
MUCOPURULENT DRAINAGE CAN BE PUSHED ASIDE TO COLLECT PAP
CAN STILL COLLECT OTHER CERVICAL STI SPECIMENS AT SAME TIME AS PAP
HPV COLLECTION SCREENING
BASIC OR PRIMARY -TESTS HPV ALONE
HPV ASSAYS DETECT FULL RANGE (HRHPV)
USU USED FOR HIGH RISK OR ABNORMAL PAP SMEAR
DONT USE TO DETECT WARTS TYPES <25 YEARS AS PART OF ROUTINE SCREEENING PAP
COTESTING ALLOWED OVER CERTAIN AGE
INTERPRETATION
BETHESDA AND PAP
I-V
BETHESDA
CIN SCALE
-SQUAMOUS LESIONS ,BASED ON FRACTION OF NORMAL EPITHELIAL CELLS REPLACED BY UNDIFFERENTIATED CELLS
CIN 1 MILD DYSPLASIA
CIN 2 MODERTAE
CIN 3 SEVERE DYSPLASIA PREMALIGANT
LAST SCALE
SQUAMOUS LESIONSTWO TIERED
LSIL LOW GRADE SQUAMOUS INTEREPITHELIAL LESIONS -CORRESPOND TO CIN 1
HSIL CORRESPOND TO CIN 3
FRO CINI 2 THEY DO IMMUNOHISTOLOGICAL STAINING OF BIOMARKER P16 -IF NEGATIVE DOWNGRADED TO LSIL, IF POSITIVE UPGRADED TO HSIL
ANAL CANCER SCREENING
NO LUBES OR ANYTHING IN RECTUM
OROPHARYNGEAL SCREENING- NOT RECOMMEDED IN ASYMPTOMATIC ADULTS
FIRST DARE - DIGITAL ANORECTAL EXAM
ANAL PAP INSERT FINGER 2-3 INCHES INTO ANAL CANAL, SWAB CIRCULAR -GLASS SLIDE OTR LIQUID
NO HPV ANAL TESTS ON MSM NOT FDA APPROVED AS MOST MSM HAVE HPV
USE ANOSCOPY
USPSTF CERVICAL CANCER SCREENING
AGE 21-65 YEARS
21-29 PAP Q 3 YEARS
30-65 3 OPTIONS
PAP Q 3YEARS
HRHPV Q 5 YEARS
COTESTING Q 5 YEARS
<21 NO SCREENING
> 65 NO SCREENING IF NO ABNORMALITIES
HPV VACCINE SCREENING IS SAME
HYSTERECTOMYAND CERVIX REMOVAL + NO HISTORY OF DYSPLASIA-NO SCREENING
ANOGENTIAL WART TREATMENT
GOAL REMOVE VISIBLE WARTS
REDUCES DOES NOT ELIMINATE TRANSISSION,OR REDUCE CANCER RISK
PROVIDER APPLIED TREATMENTS-WORK QUICKER AND FEWER TREATMENTS
PATIENT APPLIED, PRIVACY OF OWN HOME
PROVIDER:
CRYOTHERAPY + SURGICAL REMOVAL REFER
TCA-TRICHLOROACETIC ACID
BCA BICHOLORACETIC ACID
NO TCA BCA OR PODOPHYLLIN FOR URETHRAL WARTS
PATIENT:
IMIQUIMOD 3.75%CREAM Q NOCTE X 8 WEEKS-CAN WEAKEN CONDOMS AND DIAPHRAGMS
IMIQUOD 55 3XWEEK X 16 WEEKS
PODOFILOZ 0.5% GEL BID X 3 DAY THEN OFF FOR 4 DAYS , REPEAT CYCLE X SINECATECHINS 15%OINTMENT TID UPT TO 16 WEEKS
FOLLOW UP IN 3 MONTHS
CONDOM USED REDUCEDS 70%
LIKE VIRUS THE VACCINE USED RECOMBINANT TECHNOLOGY PRODUCING l1 PROTEINS THAT SLF ASSEMBLE INTO VIRAL LIKE PARTICLES
HPV 6-11-16-18-31-33-45-52-58
ONLY ADVERSE S/E IS IMMEDIATE POST INJECTION SYNCOPE
11-12 YEARS ( CAN START AT AGE 9)
>13 YEARS-26 YEARS CAN GET CATCH UP VACCINATION
27-45 SHARED DECISION MAKING
DOSING:
9-14 2 DOSE HPV 6 MONTHS APART MINIMAL 5 MONTHS APART OR GET THIRD DOSE
15 AND OVER 3 DOSE 0, 1-2 AND 6 MONTHS
INTERRUPTED SCHEDULE : COMPLETE THE SERIES WITHOUT REPEATING DOSES
NO PREGANCNY TEST REQUIRED
HIV -ALL GET 3 DOSE VACCINE
HPV INFECTION EDUCATION
MOST COUPLES SHARE HPV HISTORY
DOES NOT MEAN PARTNER IS HAVING SEX OUTSIDE RELATIONSHIP
MOST PEOPLE CLEAR INFECTION SPONTANEOUSLY WITHOUT HEALTH PROBLEMS
IF INFECTION PERSISTS
CERVIX ANAL PENIS VULVA VAGINA HEAD NECK CANCERS AND PRE CANCERS AND WARTS MAY DEVELOP
PARTNER NO TESTING- BUT COUNSELLING ON IMPLICATIONS- HIGHLY CONTAGIOUS , CONDOM USE
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