Introduction to Midwifery

Key Terminologies in Midwifery

Table of Contents

Definition

Cervical cancer (CaCx), is an abnormal, uncontrolled growth of the cells of the cervix that spread or capable of spreading to other parts of the body and interfere with normal body functions.

  • It’s one of the many cancers that affect the reproductive system and thus sexual & reproductive health.

Causes of CaCx

  • It’s caused by infection of the cervix with high risk Human Papilloma Virus (HPV) types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58 & 59.

  • HPV is sexually transmitted, peak of infection at 20-24 yrs.

  • HPV types-16, 18 & 45 account for 94% of CaCx.

  • HPV types 16 & 18 account for 70% of cases.

  • HPV type 16 is the most carcinogenic.

  • HPV types 6 & 11 cause genital warts & respiratory papillomatosis.

Progression to Cervical Cancer

StageDescription
Normal EpitheliumHealthy cervical tissue
HPV InfectionInitial viral infection
CIN1Cervical Intraepithelial Neoplasia grade 1
CIN2Cervical Intraepithelial Neoplasia grade 2
CIN3Cervical Intraepithelial Neoplasia grade 3
CarcinomaDevelopment of invasive cancer

Persistent HPV infection leads to progression from LSIL (Low-grade Squamous Intraepithelial Lesion) to HSIL (High-grade Squamous Intraepithelial Lesion) and eventually carcinoma.


Risk Factors for Cervical Cancer

  • Infection with high-risk HPV

  • Early sexual intercourse (before 20 years)

  • Having multiple sexual partners or a partner with multiple sexual partners

  • Immunosuppression (e.g., HIV infection)

  • High parity (3 or more children)

  • Local cervical trauma during childbirth

  • High rates of cervical abnormalities during pregnancy

  • High detection rate of HPV among pregnant women

Additional risk factors include:

  • Long-term use of Combined Oral Contraceptives (COCs) – Estrogen acts as an anti-apoptotic agent, promoting the proliferation of HPV-infected cells and increasing vulnerability to mutations.

  • Smoking – Smokers have twice the risk compared to non-smokers. Tobacco products are found in cervical mucus and may damage DNA, predisposing to cancer.

  • Low socioeconomic status – Associated with limited education, poverty, old age, low access to information, poor health care, and lack of screening.

  • Lack of regular screening for cervical cancer.


Signs and Symptoms of Cervical Cancer

Early stages may be asymptomatic.
Common symptoms include:

  • Abnormal vaginal bleeding: during or after sexual intercourse, between menstrual periods, or after menopause.

  • Abnormal vaginal discharge: foul-smelling, watery, thick, mucoid, bloody, or purulent (pus-like).

  • Pain: lower abdominal pain, lower back pain, and pain during sexual intercourse (dyspareunia).

  • Abnormal bowel or urinary symptoms: due to pressure on the bladder or rectum or metastasis; may present as constipation, blood in stool, rectal bleeding, hematuria, dysuria, urinary frequency, or obstruction.

On vaginal/speculum examination:

  • Abnormal cervix with cervical mass or growth (fungating), ulcer, or easily bleeding on contact.

  • The cervix may be fixed, enlarged, or hard.

  • Adnexa may be free or fixed with possible vaginal involvement.

  • Weight loss—common in advanced stages.

Over 80% of women are diagnosed at a late stage, when cure is no longer achievable. Many cases remain undocumented.


Staging of Cervical Cancer (FIGO Classification)

Stage I: Cancer confined to the cervix

  • IA: Microscopic lesions with stromal invasion ≤5 mm deep and ≤7 mm wide

    • IA1: Invasion ≤3 mm in depth

    • IA2: Invasion >3 mm depth

  • IB: Macroscopic lesions confined to the cervix

    • IB1: Lesions ≤4 cm in size

    • IB2: Lesions >4 cm in size

Stage II: Cancer extends beyond the cervix but not to pelvic wall or lower third of vagina

  • IIA: No parametrial involvement

    • IIA1: Tumor <4 cm, involves upper two-thirds of vagina

    • IIA2: Tumor >4 cm, involves upper two-thirds of vagina

  • IIB: Obvious parametrial involvement

Stage III: Tumor extends to pelvic wall and/or lower third of vagina

  • IIIA: No extension to pelvic walls but involves lower third of vagina

  • IIIB: Extension to pelvic walls or causes hydronephrosis/nonfunctioning kidneys

Stage IV: Tumor extends beyond true pelvis or involves bladder/rectum

  • IVA: Growth to adjacent pelvic organs

  • IVB: Spread to distant organs (liver, lungs)


Treatment of Cervical Cancer

StageRecommended Treatment
Stage 0 (Carcinoma in situ / CIN)Cryotherapy, LEEP (Loop Electrosurgical Excision Procedure), or Simple Total Hysterectomy
Stage IA1Total hysterectomy or radical hysterectomy
Stage IA2, IB, IIACombined radiotherapy and radical hysterectomy with bilateral pelvic lymphadenectomy
Stage IIB, III, IVACisplatin-based chemotherapy combined with radiotherapy
Stage IVB & Recurrent CancerPalliative radiotherapy or chemotherapy

Prevention of Cervical Cancer

1. Sexual Behavior Change

  • Abstinence

  • Avoiding early sexual debut

  • Avoiding multiple sexual partners

  • Consistent condom use

2. Vaccination

  • HPV vaccine (Gardasil) — quadrivalent, active against HPV types 6, 11, 16, and 18.

  • Administered as two IM injections (0 and 6 months) before sexual debut.

  • Target group: girls aged 10–14 years.

3. Cervical Cancer Screening

  • Methods:

    • Visual Inspection with Acetic Acid (VIA)

    • Visual Inspection with Lugol’s Iodine (VILI)

    • PAP smear

    • HPV DNA testing

    • Colposcopy and Cervical Biopsy

4. Early Treatment of Premalignant Lesions

  • Cryotherapy

  • LEEP

  • Thermocoagulation

WHO 2030 Targets

  • 90% of eligible girls vaccinated against HPV
  • 70% of eligible women screened at least twice in their lifetime
  • 90% of women with positive screening tests or lesions effectively treated (including palliative care)

The Four Pillars of Cervical Cancer Control

  1. Prevention of HPV infection
  2. Screening for dysplasias
  3. Early diagnosis and treatment
  4. Palliative care

Cervical Cancer Screening Methods

Early detection of cervical cancer through screening in women aged 25 years and above, followed by treatment of precancerous lesions, can prevent the majority of cases.
Screening is a public health intervention aimed at asymptomatic populations to identify individuals at increased probability of having disease or precancerous lesions.

Screening Methods:

  • VIA (Visual Inspection with Acetic Acid)

  • VILI (Visual Inspection with Lugol’s Iodine)

  • PAP smear

  • HPV DNA testing

Note: Cervical biopsy and colposcopy are diagnostic, not screening tools.


Visual Inspection with Acetic Acid (VIA)

  • Uses 3–5% acetic acid, which causes reversible protein coagulation in tissues with high DNA concentration—appearing white (“acetowhite”).

  • Physiologic conditions with high nuclear activity that may transiently turn white: mature metaplasia and columnar epithelium.

Procedure:

  1. Place patient in lithotomy position.

  2. Insert and adjust speculum.

  3. Remove discharge using dry or saline-soaked cotton swab.

  4. Apply acetic acid to cervix and wait one minute.

Indications:

  • Used in women below 50 years (with visible squamocolumnar junction).

  • For postmenopausal women (SCJ recedes), use PAP smear instead.


Visual Inspection with Lugol’s Iodine (VILI)

  • Uses 5% Lugol’s iodine, a glycophilic solution staining glycogen-rich tissues dark brown.

  • Normal mature squamous epithelium → dark brown

  • Columnar epithelium → pinkish (no glycogen)

  • Precancerous/glycogen-poor tissues → yellow

Physiologic glycogen-poor states (iodine negative):

  1. Columnar epithelium (pinkish)

  2. Postmenopausal/hypo-estrogenic states (yellow)

A VILI positive area may indicate benign lesion, precancerous lesion, or cancer.

PAP Smear

  • Sample from vagina and cervix applied to slide for cytopathological analysis.


HPV DNA Testing

  • Detects presence of HPV in the cervix.

  • More expensive than other methods.


Colposcopy

  • Uses a colposcope (magnifying device).

Indications:

  • Abnormal cytology

  • Grossly abnormal cervical lesions (even if cytology negative)

  • Postcoital bleeding (even if smear negative)


Re-screening Intervals

  • HIV-positive women: every 1 year

  • HIV-negative women: every 3 years

  • Post-treatment follow-up (LEEP or cryotherapy for CIN2/CIN3): after 1 year


Treatment of Precancerous Lesions

Cryotherapy

  • Uses cryoprobes, cryogun, pressure gauge, and stopwatch.

  • Metal probe cooled by CO₂ or N₂O gas freezes abnormal ectocervical tissue (destructive therapy).

  • No anesthesia needed.

Procedure:
Two successive freeze–thaw cycles:

  • 3-minute freeze → 5-minute thaw → repeat

Indications:

  • CIN 2–3 lesions not suspicious of cancer

  • Lesions fully covered by cryoprobe

  • No >2 mm endocervical canal extension

  • Not used in pregnancy

Side effects: mild pelvic pain, watery discharge, light bleeding up to 2 weeks, rarely infection or cervical stenosis.

Loop Electrosurgical Excision Procedure (LEEP)

  • Uses fine stainless steel or tungsten wire loop electrodes (0.2 mm) to excise the transformation zone containing lesions.

  • Indicated for:

    • Early-stage suspicious lesions

    • Lesions ineligible for cryotherapy/thermocoagulation

    • Lesions with >2 mm endocervical extension

  • Not used in pregnancy

Side effects: similar to cryotherapy and thermocoagulation. Rarely, may cause:

  • Spontaneous miscarriage (due to cervical incompetence)

  • Prolonged labor (due to cervical stenosis)


Thermocoagulation

  • Uses a probe heated to 100°C to destroy ectocervical abnormal tissue (destructive therapy).

  • Performed without anesthesia.

Procedure:

  • Single application lasting 60 seconds.

Indications:

  • CIN 2–3 lesions not suspicious of cancer

  • Lesions ≤2 mm endocervical extension

  • Not used in pregnancy

Side effects: mild pelvic pain, watery discharge, spotting or light bleeding for 2 weeks, rarely infection or cervical stenosis.

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