Abnormal pap smear

Published on 10/03/2015 by admin

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Last modified 22/04/2025

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Chapter 1 ABNORMAL PAP SMEAR (ABNORMAL CERVICAL CYTOLOGIC FINDINGS)

Cervical cytology screening has significantly decreased rates of mortality from cervical cancer; however, 400 women die each year in the United States from cervical cancer, mostly as a result of inadequate screening.

Cervical cytology results are classified according to the Bethesda 2001 system (Box 1-1), which describes the categories of epithelial cell abnormalities. Histologic diagnoses of abnormalities are reported as cervical intraepithelial neoplasia (CIN) grades 1-3.

The glandular cell abnormalities are reported under the following categories: atypical glandular cells (AGC), subcategorized as endocervical, endometrial, or glandular not otherwise specified; AGC, favor neoplastic; endocervical adenocarcinoma in situ; and adenocarcinoma. Also noted are the presence of organisms, including Trichomonas vaginalis and fungal organisms morphologically consistent with Candida species; shift in flora suggestive of bacterial vaginosis; the presence of bacteria morphologically consistent with Actinomyces species; and cellular changes consistent with herpes simplex virus. Other findings that are noted include reactive cellular changes associated with inflammation, radiation, presence of intrauterine device, glandular cell status post hysterectomy, and atrophy.

In 2003, the U.S. Preventive Services Task Force recommended that all women be screened for cervical cancer with a cervical cytologic work-up beginning at age 21 or 3 years after sexual activity begins, whichever occurs first. Screening then should be performed at least every 3 years. Women who are older than 65 years need not undergo routine screening for cervical cancer if they have had appropriate screening and normal Pap smear results in the past. In addition, women who have had a total hysterectomy for a benign reason should not undergo screening for cervical cancer.

Most cases of cervical cancer are associated with infection with high-risk types of human papillomavirus (HPV) which are types 16, 18, 31, 33, 45, 51, 52, 56, 58, 5, 68, 73, and 82. HPV testing is used as an adjunct to the cervical cytologic work-up in women aged 30 years and older, as well as in cases of atypical squamous cells of undetermined significance (ASC-US) to determine whether a colposcopy should be performed.

Other risk factors for cervical cancer include cigarette smoking, immunocompromised status (e.g., human immunodeficiency virus [HIV] infection), early age at onset of sexual activity, multiple sexual partners, and sexual activity with male partners at high risk for sexually transmitted diseases.

Suggested Work-Up

The Bethesda 2001 classification system was used to create the American Society for Colposcopy and Cervical Pathology Consensus Guidelines in 2001 to distinguish women at risk for significant cervical disease from those with mild or no disease. The American College of Obstetrics and Gynecology also published guidelines for the management of abnormal Pap smears/cervical cytologic findings (Figs. 1-1 to 1-5). The guidelines involve substantial use of HPV DNA testing and colposcopy. Other testing used includes endocervical sampling, biopsy, and excisional procedures.

In pregnant women, endocervical sampling is not indicated and biopsies should be performed only for visible lesions that appear to be CIN grade 3, adenocarcinoma in situ, or cancer. In addition, excisional procedures should be considered in pregnant women only if a lesion discovered at colposcopy appears to be invasive cancer.

The following are recommendations for evaluation that are based upon cervical cytologic results. Algorithms are provided in Figures 1-1 to 1-5.

ASC-US If HPV testing is positive, colposcopy should be performed with consideration of endocervical sampling with a brush or curette; if finding is negative, then the Pap smear should be repeated in 1 year
  If HPV test result is negative, then a Pap smear should be repeated in 1 year; if HPV testing is not performed, other options include immediate colposcopy or repeat Pap smear at 6 and 12 months
  If the patient is immunocompromised, then colposcopy should be performed immediately
  In adolescents with ASC-US who are HPV positive, Pap smears may be repeated at 6 and 12 months or HPV testing may be undertaken at 12 months instead of immediate colposcopy, since clearance rate of HPV is high
ASC-H Colposcopy should be performed with consideration of endocervical sampling
LSIL Colposcopy should be performed with consideration of endocervical sampling
  In adolescents with LSIL, Pap smears may be repeated at 6 and 12 months or HPV testing may be repeated at 12 months instead of immediate colposcopy, since the clearance rate of HPV is high
HSIL Colposcopy with endocervical sampling and biopsy should be performed. If the colposcopic finding is negative or inconclusive, then an excision should be performed
AGC Colposcopy and endocervical sampling should be performed
  Endometrial sampling should be performed if the patient is older than 35 years or is at risk for endometrial cancer (abnormal bleeding, obesity, or oligomenorrhea)
  Figure 1-1 to 1-4 outlines the management of AGC based on initial cytology results.
AGC, favor neoplasia, or adenocarcinoma in situ If the previously described work-up for AGC does not show invasive disease, then a diagnostic excisional procedure should be performed (cold-knife conization is preferred)

Additional Work-Up

Test for HIV infection In patients at risk
Chlamydia and gonorrhea cultures or a nucleic acid amplification test In patients at risk
Urine pregnancy test Should be performed before an invasive procedure if the patient may be pregnant
Wet mount evaluation To evaluate for Candida infection, bacterial vaginosis, or Trichomonas infection if any of these conditions is suspected