Colposcopy is a technique used to examine the cervix that was developed in 1925. It allows physicians to better define and delineate abnormalities found during cervical screening. Technological advances like computer imaging and telecolposcopy have improved colposcopy. The document outlines the history, current uses, and future of colposcopy. It discusses indications, diagnostic criteria, management recommendations, and challenges in colposcopy practice. The future of colposcopy is focused on greater use of digital imaging and telemedicine to improve patient care and quality control in a more cost-effective manner.

1. Colposcopy
Prof. Aboubakr Elnashar
Benha University Hospital. EGYPT
E-mail: elnashar@hotmail.comABOUBAKR ELNASHAR

2. •The colposcope was first developed in 1925 & is
well established in gynecologic practice for defining
& delineating cytologically detected lesions mainly of
the cervix but also the vagina & vulva.
•Colpscopy is now gradually spreading allover the
world & postgraduate training courses is now being
given in many centers.
ABOUBAKR ELNASHAR

3. Historic events related to colposcopy
1925: Invention of colposcope(Hinselman)
1928: Schiller test
1938: Acetic acid test (Hinselman)
1939: Green filter (Kratz)
1940: Pap test
1942: First photographs of cervix (Treite)
1960: Cryosurgery
1980: Laser surgery
1988: Computer-aided colposcope
1989: LLETZ (Prendiville & Cullimore)
1991: Pap Net
2000: Telecolposcopy ( Harper et al)ABOUBAKR ELNASHAR

4. Technologic advances
• New optical lenses, fiberoptic light cables &
videocameras with digital computer enhancement,
all played a part in advances of colposcopy.
•Computer technology has made it possible to
capture images directly onto a computer & these
images allow enhancement & manipulation
according to physician,s preference.
ABOUBAKR ELNASHAR

5. Colposcope Video camera
(CCD)
Optical interface
Video monitorVideo digitizer
board
PrinterPersonal computerMass storage
Digital imaging colposcopy
(CCD=charge couple device)
ABOUBAKR ELNASHAR

6. Telecolposcopy
(Harper et al,2000)
*System incorporating a custom software package.
*All images were received without distortion in color,
size, or orientation.
*technically feasible,
can be implemented in an office system with limited
technical support
preferred by women who have to travel many miles to
receive referral health care.
ABOUBAKR ELNASHAR

7. Current indications of colposcopy
1. Part of any gynecologic examination
2. Primary screening for cervical cancer.
3. Clinically suspicious cervix.
4. Abnormal Pap smear.
5. Evaluation & treatment of CIN.
6. Follow up after conservative therapy of CIN.
7. Postcoital bleeding.
8. Patients with external vulval warts
9. Evaluation of sexual assault victims.
10. Patients with history of DES exposure
ABOUBAKR ELNASHAR

8. Uses
•Screening colposcopy is a feasible procedure &
more sensitive & more cost effective than cytological
screening. When access to cytopathology is difficult,
screening colposcopy is an alternative
(Cecchini et al,1997).
•Portable colposcopy in rural areas is cost effective
& highly acceptable
(Martin et al,1998).
•The colposcopy improved detection of genital
trauma in adult female sexual assault victims as
compared with gross visual examination alone
(Lenahan,1998).
ABOUBAKR ELNASHAR

9. Recent recommendations of FIGO for management of abnormal
smear( Benedet,2000)
Persistent inflam., persistent ASCUS, LSIL, HSIL, AGCUS,Invasive
Colposcopy±biopsy
Normal or LSIL HGSIL Invasive
6 mo smear x 2 LEEP Appropriate TT
Normal Persistent
Annual screening ABOUBAKR ELNASHAR

10. Steps
• Lugols’iodine test: beneficial test..
• ECB has replaced ECC: easier to use,
malleable & less expensive.
Its specificity 92%, sensitivity 90% & positive
predictive value 88%
(Martin et al, 1995).
• Punch biopsy: False negative rate up to
54%
(Buxton et al,1991)
Multiple biopsies
Excisional techniques are superior to
destructive techniquesABOUBAKR ELNASHAR

11. Diagnostic criteria
1. Vascular pattern
2. Inercapillary distance
3. Contour.
4. Color
5. Clarity of demarcation
6. Appearance of gland opening.
7. Negativity after iodine test
ABOUBAKR ELNASHAR

12. 8. Whiteness after acetic acid:
Density of whiteness, time needed to appear &
disappear, demarcation.
Changes >35 yr are thinner & less demarcated.,
punch biopsy
(Zahm et al, 1998).
9. Surface extent of the lesion:
more important prognostic indicator for invasion than
histological gradin
(Tidbury et al,1992)
ABOUBAKR ELNASHAR

13. International Federation of Cervical Pathology &
Colposcopy(1991)
Normal: Original squamous epithelium
Columnar epithelium
Normal transformation zone
Abnormal: Acetowhite epithelium Punctation
Mosaicism Leukoplakia
Iodine negative Atypical vessels
Suspect invasive cancer:
Unsatisfactory:SCJ not visible, severe inflam or atrophy, invisible cervix
Miscellaneous:Nonacetowhite micropapillary surface,
exophytic condyloma, inflammation, atrophy, ulcer
ABOUBAKR ELNASHAR

14. Niekerk (1998)
Low grade High grade
•Acetowhite epithelium: shiny or snow dull, oyster white color
white,semitransparent
•Surface: flat irregular contour, microexophytic
•Demarcation: diffuse, irregular, sharp, straight line,
flocculated, feathered,
internal demarcation absent internal demarcation present
•Vessels: fine, regular shape, uniform coarse, dilated, increased ICD,
caliber, normal arborization, spaghetti bizarre, commas, corkscrews
changing calibers sharp bends
•Iodine: uniform mahogany brown mustard yellow, yellow or iodine -ve
ABOUBAKR ELNASHAR

15. Update of colposcopy of genital HPV
Meisels et al (1982): Florid, spiked, flat, condylomatous .
. vaginitis.
Flat condyloma & mild dysplasia represent the same biologic
phenomenon, namely, productive HPV infection (Reid,1993).
The expression of viral activity may be clinical or subclinical
when it is recognizable only on colposcopy.
Exophytic & flat condylomata are not homologous diseases.
Exophytic is usually caused by cutaneotropic viruses (6,11). Flat
are more likely to contain medium(31,33) or high risk(16,18) HPV
types.
Micropapillary condyloma should not be confused with
micropapillomatous labialis.
ABOUBAKR ELNASHAR

16. Colposcopy of the vulva
*Steps:
1. Examination after smearing with a water soluble
lubricant.
2. Prolonged acetic acid test
3. Toludine blue test: little clinical value.
* The junction between the glycogen bearing vaginal
epithelium & keratin producing vulval epithelium: high
risk for intraepithelial neoplasia.
*Abnormalities: diffuse acetowhite, localized
acetowhite, leukoplakia, micropapillae, papules.
ABOUBAKR ELNASHAR

17. Update on colposcopy in pregnancy
Difficult. & reserved for the most experienced
colposcopist.
Reassurance of the patient.
ECC is contrindicated & one directed biopsy.
Large speculum is usually needed
Sponge forceps to remove the mucous & acetic a as a
mucolytic
Unsatisfactory colposcopy: repeat after 8 w
The aim is to exclude cancer
CIN: follow up & definitive treatment 1-2 mo
postpartum.
ABOUBAKR ELNASHAR

18. Pitfalls in practice of colposcopy
A. In the technique
1. Failure to use a diagnostic protocol
2. Deviation from a diagnostic protocol.
3. Failure to visualize TZ.
B. In diagnosis
1. Misinterpretation of exagerated patterns of
pregnancy, previously treated cervix, carvical cancer.
2. Failure to select appropriate biopsy sites, enough
biopsies, sufficient volume of tissue.
3. Failure to accurately record colposcopic findings
ABOUBAKR ELNASHAR

19. C. In management
1. Miscommunication with the pathologist.
2. Failure to correlate cytology, colposcopy &
histopathology.
3.Destructive therapy without biopsy, for invasive or
glandular lesions.
D. In the colposcopist
1. Inadequate training.
2. Inadequate experience.
3. Inadequate understanding of the disease.
4. Failure to keep up with scientific developments
5. Failure to maintain skills.
6. Failure to seek consultation.
ABOUBAKR ELNASHAR

20. Diploma of colposcopy
•No one should be allowed to practice colposcopy
without having proper training or without a diploma
in colposcopy
(Jordan,1995).
•It would be a legal document that would safeguard
the public & raise the status of the colposcopist.
ABOUBAKR ELNASHAR

21. Future research in colposcopy
(Hilgarth,1998)
1. Computerized colposcopic documentation &
consecutive analysis of colposcopic findings.
2. Clinical significance & biologic behavior of minor
lesions visible with colposcopy in the presence of
different HPV types.
3. Clinical significance & relation to HPV infection of
minor lesions beyond the TZ.
4. Vulvar lesions in vulvodynia related to HPV
infection.
ABOUBAKR ELNASHAR

22. Future of colposcopy
(Niekerk,1998)
1. There are going increasing costs of medical care
& the demand for better quality control will intensify.
2. Technical advances will revolutionize this area &
digital imaging, the storage of up to 4.500 images on
an optical disk & rapid teletransmission of images
will become practical..
The use of these new technologies for better & more
cost effective patient care is the challenge we will
have to meet in the 21st century.
ABOUBAKR ELNASHAR

23. Benha University Hospital. EGYPT
ABOUBAKR ELNASHAR