Colposcopy of Preinvasive and Invasive Cervical Cancers
Kenneth D. Hatch
GENERAL PRINCIPLES
Definition
Colposcopy is a diagnostic procedure performed to examine the cervix when an abnormal Pap smear or positive human papillomavirus (HPV) is obtained on cervical screening. It utilizes a bright light source coupled with a variable magnifying microscope called a colposcope.
Anatomic Considerations
The portion of the cervix that extends into the vagina is called the portio vaginalis. The vagina and most of the cervix are lined by a smooth, pink, glycogenated, squamous epithelium. The red portion is the columnar epithelium. Metaplasia is a normal process where the columnar epithelium is replaced by a squamous epithelium under the influence of the lowered pH of the adult vagina. The outer border is the original squamous epithelium and the inner border is the squamocolumnar junction. The area in between is the transformation zone (T-zone). The immature T-zone is the area of active metaplasia where the squamous cells are advancing over the columnar cells. This is most active at menarche and in the postpartum state. The immature metaplastic cells are the most susceptible to infection by the HPV. The mature T-zone is composed of metaplastic cells that have matured into glycogen-containing squamous cells that are resistant to HPV. The figure (Fig. 15.1) illustrates the advancing squamocolumnar epithelium.
SURGICAL MANAGEMENT
Positioning
Lithotomy.
PROCEDURES AND TECHNIQUES
Basic Colposcopy
The vulva and anus are inspected as HPV is an anogenital virus. The speculum is advanced slowly, viewing the vagina as the speculum is inserted. The cervix is then exposed and examined at the various magnifications by cleansing with a cotton ball. After thorough inspection and no lesions seen, 3% to 5% of acetic acid will be placed. It should stay in contact with the cervix for 2 minutes as some lesions will react slowly.
For the initial inspection, the colposcope should be at low power (4× to 6×) to see any obvious cancer lesions; then higher power 10×, 16×, and even 25× is used.
It is important to recognize the appearance of the normal T-zone. The tech figure (Tech Fig. 15.1) shows the immature T-zone. The metaplastic cells will become slightly gray in appearance. The columnar cells will be red. Metaplastic squamous cells will extend over the columnar cells and eventually replace them. The tech figure (Tech Fig. 15.2) is a higher-power view of this process.
The tech figure (Tech Fig. 15.3) shows a more mature T-zone. There is an area of mature metaplastic squamous cells and an area of active metaplasia at the squamocolumnar junction. In the mature epithelium, some normal gland openings can be seen.
Abnormal transformation zone—squamous intraepithelial lesions
The goal of colposcopy is to identify the cervical intraepithelial neoplasia (CIN) and invasive cancer. The term CIN is used for the squamous precancers; it is not used for the adenocarcinoma precursors. The CIN cells have nuclei that are larger and darker than normally maturing squamous cells. The application of 5% acetic acid causes the cytoplasm to shrink and make the nuclei even more prominent. When the light of the colposcope hits the CIN, the light is reflected back like a mirror, giving the white appearance. The normal cells are translucent and the light goes through to the blood vessels below, and the cervix appears pink. The columnar cells will appear red because they are a single layer over the vascular network. The tech figure (Tech Fig. 15.4) shows a illustration depicting the CIN versus normal epithelium. The acetic acid should be applied for 1.5 to 2 minutes with the scope in focus and the examiner watching the T-zone for acetowhite change. In addition to the appearance of acetowhite, the vascular changes of punctation and mosaic may appear. Punctation vessels are formed by the preservation of the columnar vessels in the neoplastic epithelium (Tech Fig. 15.5). The mosaic vessels are formed by the network of vessels around the glands that the CIN replaces (Tech Fig. 15.6).
Tech Figure 15.4. The CIN cells have large nuclei which reflect the light while the normal cells have small nuclei which allow the light to penetrate.
The colposcopist will observe for up to 5 minutes with reapplication of acetic acid, if needed. The T-zone will be described as normal if no lesion is seen or abnormal if a lesion is seen. The examination will be termed satisfactory if the entire T-zone is seen and unsatisfactory if it is not.
The most common reason for unsatisfactory is that the lesion goes into the cervical canal. If a lesion is seen, it will be described as low grade if it is CIN 1 or high grade if it is CIN 2 or 3. It will be described as suspect invasive cancer if there are ulcerations, abnormal vessels, or a necrotic surface. The findings used to determine grade are the denseness of the acetowhite change, the distinctness of the border, and the appearance of vascular changes of punctation and mosaic. In 2012, the International Federation of Colposcopy and Cervical Pathology (IFCPC) added three additional signs of CIN 3. They are cuffed-gland sign, inner border sign, and ridge sign.
Low-grade lesions have less dense acetowhite, indistinct borders, and do not have punctation or mosaic (Tech Fig. 15.7). High-grade lesions include CIN 2 and CIN 3. Since CIN 2 lesions may not be treated in young women, it may be useful to separate them from CIN 3 based on the IFCPC criteria above. Additional criteria are the coarseness of the punctation and mosaic. An example of CIN 2 is shown in the tech figure (Tech Fig. 15.8). It has a distinct border with dense acetowhite, but there are no vessels and none of the other IFCPC signs of CIN 3. Lugol solution is used to allow the colposcopist to see the border distinctly and differentiate it from CIN 1 (Tech Fig. 15.9). Punctation and mosaic are shown in tech figure (Tech Fig. 15.10). Here, a cotton-tipped applicator is used to lift the anterior lip of the cervix
to see that the examination is satisfactory. This is CIN 3. The tech figure (Tech Fig. 15.11) shows the inner border sign of an oncogenic HPV. Peripheral to that is the irregular border of a non-oncogenic HPV. This border is indistinct and not thick. There is mosaic as one looks toward the squamocolumnar junction. The tech figure (Tech Fig. 15.12) shows a higher power
of the mosaic area of this patient. The tech figure (Tech Fig. 15.13) shows the cuffed-gland sign and the ridge sign. Both are indicative of CIN 3. The tech figure (Tech Fig. 15.14) shows cuffed glands, irregular mosaic, and another finding called rag sign where the epithelium has peeled away from the stroma. The tech figures (Tech Figs. 15.15, 15.16 and 15.17) show the same patient before acetic acid, after acetic, and when the acetic is wearing off. It shows the thick acetowhite can cover the mosaic and emphasizes why the examiner must observe for up to 5 minutes. The tech figure (Tech Fig. 15.18) shows a large CIN 3 that does not have much acetowhite effect but has cuffed glands, mosaic, and extends into the endocervix. These extensive lesions are difficult to encompass with the wire loops used for loop electrosurgical
excision procedure (LEEP), and a cone should be considered to rule out invasion. The tech figures (Tech Figs. 15.19 and 15.20) are describing the same patient. Again there is very little acetowhite, but there are cuffed-gland openings. This is a large lesion but the examination is satisfactory. The tech figures (Tech Figs. 15.21 and 15.22) are describing the same patient.Stay updated, free articles. Join our Telegram channel
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