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ABNORMAL CERVICAL SMEAR –
PROCEDURE SCREENING &
MANAGEMENT
OPS UNIT
OUTLINE
• Introduction: Pap smear
• Overview: Cervical cancer
• Pap smear procedure
• Pap smear findings
• Management
• Conclusion
• References
• A cervical smear is a cytology-based screening test for cervical
cancer in which vaginal cells are collected and stained as a means of
detecting cytologic abnormalities of the uterine cervix.
• Developed by Dr George Papanicolaou in 1943.
• It has been implemented in countries around the world as a
screening strategy, and subsequent reductions in rates of cervical
cancer by 50% or more have been seen.
• It is recommended to be performed once every 3-5 years for women
between the ages of 25 to 65 years.
• The reported sensitivity and specificity of Pap smear varies: sensitivity
ranges from 30-87%, and specificity ranges from 86-100%.
INTRODUCTION
INTRODUCTION
• For more than 95% of women, cervical cytology is normal
and normal squamous cells are seen.
• Abnormal cervical cytology shows squamous cells at different
stages of maturity(dyskaryosis).
• When abnormal cells are detected on the pap smear,
diagnostic testing in the form of colposcopy is often indicated.
• 2nd most common cancer among women in developing
countries.
• Most common gynaecological cancer and a leading cause of
cancer deaths among women in Nigeria.
• Established aetiology is a persistent Human Papillomavirus
infection (most implicated serotypes are high-risk 16 and 18),
mainly acquired from sexual contact.
• Risk factors include: early coitarche, multiple sexual partners,
promiscuous male partners, history of STIs,
immunosuppression (HIV), multiparity, COCP use, smoking.
CERVICAL CANCER
PAP SMEAR PROCEDURE
Preparation
• Cervical screening should be done when the patient is not menstruating.
• Avoid vaginal intercourse, douching, use of tampons, use of medicinal
vaginal or contraceptive cream for 24-48 hours prior to the test.
• Ideally, pre-existing cervicitis should be treated prior to cervical screening.
• Screening should proceed in the presence of bleeding or cervicitis, as
these symptoms may be related to cervical dysplasia or neoplasia.
PAP SMEAR PROCEDURE
Positioning
• Patient should be supine, in dorsal
lithotomy position to correctly
perform the procedure.
• The coccyx of the patient should be
at the edge of the examination table
to provide adequate visualization of
the cervix once the speculum is
inserted.
• Cervix is visualized using a speculum.
• Samples of the cervix are taken from the transformation zone; where the
ectocervix and endocervix meet and where dysplasia is most likely to be
identified.
• Samples are taken using an Ayres spatula.
• Smear spread on a slide and the slide fixed in 90% ethanol.
• Smear is sent to a cytopathologist, who provides a cytologic analysis.
PAP SMEAR PROCEDURE
PAP SMEAR FINDINGS
• Pap smear results are routinely reported according to the
Bethesda system.
• The Bethesda system provides a framework for consistent
interlaboratory terminology for the reporting of
cervicovaginal cytology specimens.
• Most recent update to the system was done in 2014.
• A satisfactory smear should have squamous cells, metaplastic
cells and columnar cells.
THE BETHESDA SYSTEM
• Specimen Type
• Specimen Adequacy
• General categorization*
• Interpretation/Results
• Ancillary Testing
• Automated Review
• Educational Notes & Suggestions
Negative for Intraepithelial Lesion or Malignancy (NILM)
• Non-Neoplastic Findings (non-neoplastic cellular variations, reactive cellular
changes, glandular cells)
• Organisms
Epithelial Cell Abnormality
• Squamous Cell
• Atypical squamous cells: of undetermined significance (ASC-US) OR cannot
exclude HSIL (ASC-H)
• Low-grade squamous intraepithelial lesion (LSIL) (encompassing: HPV/mild
dysplasia/CIN 1)
• High-grade squamous intraepithelial lesion (HSIL) (encompassing: moderate
and severe dysplasia, CIS; CIN 2 and CIN 3)
• Squamous cell carcinoma
BETHESDA SYSTEM (2014) – GENERAL CLASSIFICATION (1)
Epithelial Cell Abnormalities (cont.)
• Glandular Cell
• Atypical endocervical cells OR endometrial cells OR glandular
cells (NOS or specify in comments)
• Atypical endocervical cells (favour neoplastic) OR glandular
cells (favour neoplastic)
• Endocervical adenocarcinoma in situ
• Adenocarcinoma: endocervical, endometrial, extrauterine,
not otherwise specified (NOS)
BETHESDA SYSTEM (2014) – GENERAL CLASSIFICATION (2)
ASC-US and ASC-H cells
• Degree of nuclear atypia is not sufficient for the cells to be defined as either a high-grade
or low-grade squamous intraepithelial lesion.
Low-grade squamous intraepithelial lesions
• Suggestive of mild dysplasia or expected CIN-1 on histology and HPV infections with
high-risk types. Approximately 50% will regress, while 20% will progress to HSILs in 24
months.
High-grade squamous intraepithelial lesions
• Consistent with moderate and severe dysplasia, corresponding with CIN-2, CIN-3, and
carcinoma in-situ on histology. Only 35% will regress.
PAP SMEAR FINDINGS – CYTOLOGIC ABNORMALITIES
• Cervical Intraepithelial Neoplasia (CIN) is a precancerous lesion of the cervix
• Identified in cytology by:
• Koilocytes (atypical cells with a perinuclear cavitation or halo in the
cytoplasm)
• Dysplastic cells with increased nucleo-cytoplasmic ratio.
• Low-grade CIN/CIN-1: one-third of epithelial thickness has dysplastic
changes
• CIN-2: half to two-thirds of epithelial thickness has dysplastic changes
• CIN-3: full-thickness involvement of epithelium
• Carcinoma in-situ: dysplasia seen throughout the epithelium, resembles
cervical cancer, but no basement membrane invasion.
PAP SMEAR FINDINGS – CIN
NILM
• Repeat in 3-5 years as recommended
ASC-US
• Repeat cytology in 1 year; if negative, repeat cytology in 3 years
• HPV testing is preferred; if negative, repeat cotesting in 3 years; if
positive, perform colposcopy
ASC-H cells, LSIL, HSIL
• Perform colposcopy
Colposcopy involves visualization the cervix and obtaining biopsies of
lesions identified by acetic acid stain (sharp, distinct, well defined, dense
aceto-white lesions).
MANAGEMENT (1)
Precancerous lesions can be treated via:
• Ablative Methods
• Cryotherapy
• Laser
• Cold coagulation
• Excisional Methods
• Large Loop Excision of the Transformation Zone (LLETZ)/Loop Electrosurgical Excision
Procedure (LEEP)
• Laser cone biopsy
• Cold knife cone biopsy
• Hysterectomy (in cases of co-existing uterine conditions such as fibroids)
Annual follow-up with Pap smears following treatment of precancerous lesions.
MANAGEMENT (2)
CONCLUSION
Cervical/Pap smear is a useful screening tool to control the most common gynaecological
cancer among women in Nigeria.
REFERENCES
1. Cervical Screening: Overview, Human Papillomavirus, Papanicolaou Test. 2021 Aug 22
[cited 2022 Mar 10]; Available from: https://emedicine.medscape.com/article/1618870-
overview
1. Gynaecology by ten teachers, 20E
1. HPV and premalignant disease of the cervix by Prof Anorlu

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Abnormal Cervical Smear Presentation .pptx

  • 1. ABNORMAL CERVICAL SMEAR – PROCEDURE SCREENING & MANAGEMENT OPS UNIT
  • 2. OUTLINE • Introduction: Pap smear • Overview: Cervical cancer • Pap smear procedure • Pap smear findings • Management • Conclusion • References
  • 3. • A cervical smear is a cytology-based screening test for cervical cancer in which vaginal cells are collected and stained as a means of detecting cytologic abnormalities of the uterine cervix. • Developed by Dr George Papanicolaou in 1943. • It has been implemented in countries around the world as a screening strategy, and subsequent reductions in rates of cervical cancer by 50% or more have been seen. • It is recommended to be performed once every 3-5 years for women between the ages of 25 to 65 years. • The reported sensitivity and specificity of Pap smear varies: sensitivity ranges from 30-87%, and specificity ranges from 86-100%. INTRODUCTION
  • 4. INTRODUCTION • For more than 95% of women, cervical cytology is normal and normal squamous cells are seen. • Abnormal cervical cytology shows squamous cells at different stages of maturity(dyskaryosis). • When abnormal cells are detected on the pap smear, diagnostic testing in the form of colposcopy is often indicated.
  • 5. • 2nd most common cancer among women in developing countries. • Most common gynaecological cancer and a leading cause of cancer deaths among women in Nigeria. • Established aetiology is a persistent Human Papillomavirus infection (most implicated serotypes are high-risk 16 and 18), mainly acquired from sexual contact. • Risk factors include: early coitarche, multiple sexual partners, promiscuous male partners, history of STIs, immunosuppression (HIV), multiparity, COCP use, smoking. CERVICAL CANCER
  • 6. PAP SMEAR PROCEDURE Preparation • Cervical screening should be done when the patient is not menstruating. • Avoid vaginal intercourse, douching, use of tampons, use of medicinal vaginal or contraceptive cream for 24-48 hours prior to the test. • Ideally, pre-existing cervicitis should be treated prior to cervical screening. • Screening should proceed in the presence of bleeding or cervicitis, as these symptoms may be related to cervical dysplasia or neoplasia.
  • 7. PAP SMEAR PROCEDURE Positioning • Patient should be supine, in dorsal lithotomy position to correctly perform the procedure. • The coccyx of the patient should be at the edge of the examination table to provide adequate visualization of the cervix once the speculum is inserted.
  • 8. • Cervix is visualized using a speculum. • Samples of the cervix are taken from the transformation zone; where the ectocervix and endocervix meet and where dysplasia is most likely to be identified. • Samples are taken using an Ayres spatula. • Smear spread on a slide and the slide fixed in 90% ethanol. • Smear is sent to a cytopathologist, who provides a cytologic analysis. PAP SMEAR PROCEDURE
  • 9.
  • 10. PAP SMEAR FINDINGS • Pap smear results are routinely reported according to the Bethesda system. • The Bethesda system provides a framework for consistent interlaboratory terminology for the reporting of cervicovaginal cytology specimens. • Most recent update to the system was done in 2014. • A satisfactory smear should have squamous cells, metaplastic cells and columnar cells.
  • 11. THE BETHESDA SYSTEM • Specimen Type • Specimen Adequacy • General categorization* • Interpretation/Results • Ancillary Testing • Automated Review • Educational Notes & Suggestions
  • 12. Negative for Intraepithelial Lesion or Malignancy (NILM) • Non-Neoplastic Findings (non-neoplastic cellular variations, reactive cellular changes, glandular cells) • Organisms Epithelial Cell Abnormality • Squamous Cell • Atypical squamous cells: of undetermined significance (ASC-US) OR cannot exclude HSIL (ASC-H) • Low-grade squamous intraepithelial lesion (LSIL) (encompassing: HPV/mild dysplasia/CIN 1) • High-grade squamous intraepithelial lesion (HSIL) (encompassing: moderate and severe dysplasia, CIS; CIN 2 and CIN 3) • Squamous cell carcinoma BETHESDA SYSTEM (2014) – GENERAL CLASSIFICATION (1)
  • 13. Epithelial Cell Abnormalities (cont.) • Glandular Cell • Atypical endocervical cells OR endometrial cells OR glandular cells (NOS or specify in comments) • Atypical endocervical cells (favour neoplastic) OR glandular cells (favour neoplastic) • Endocervical adenocarcinoma in situ • Adenocarcinoma: endocervical, endometrial, extrauterine, not otherwise specified (NOS) BETHESDA SYSTEM (2014) – GENERAL CLASSIFICATION (2)
  • 14. ASC-US and ASC-H cells • Degree of nuclear atypia is not sufficient for the cells to be defined as either a high-grade or low-grade squamous intraepithelial lesion. Low-grade squamous intraepithelial lesions • Suggestive of mild dysplasia or expected CIN-1 on histology and HPV infections with high-risk types. Approximately 50% will regress, while 20% will progress to HSILs in 24 months. High-grade squamous intraepithelial lesions • Consistent with moderate and severe dysplasia, corresponding with CIN-2, CIN-3, and carcinoma in-situ on histology. Only 35% will regress. PAP SMEAR FINDINGS – CYTOLOGIC ABNORMALITIES
  • 15. • Cervical Intraepithelial Neoplasia (CIN) is a precancerous lesion of the cervix • Identified in cytology by: • Koilocytes (atypical cells with a perinuclear cavitation or halo in the cytoplasm) • Dysplastic cells with increased nucleo-cytoplasmic ratio. • Low-grade CIN/CIN-1: one-third of epithelial thickness has dysplastic changes • CIN-2: half to two-thirds of epithelial thickness has dysplastic changes • CIN-3: full-thickness involvement of epithelium • Carcinoma in-situ: dysplasia seen throughout the epithelium, resembles cervical cancer, but no basement membrane invasion. PAP SMEAR FINDINGS – CIN
  • 16. NILM • Repeat in 3-5 years as recommended ASC-US • Repeat cytology in 1 year; if negative, repeat cytology in 3 years • HPV testing is preferred; if negative, repeat cotesting in 3 years; if positive, perform colposcopy ASC-H cells, LSIL, HSIL • Perform colposcopy Colposcopy involves visualization the cervix and obtaining biopsies of lesions identified by acetic acid stain (sharp, distinct, well defined, dense aceto-white lesions). MANAGEMENT (1)
  • 17.
  • 18.
  • 19. Precancerous lesions can be treated via: • Ablative Methods • Cryotherapy • Laser • Cold coagulation • Excisional Methods • Large Loop Excision of the Transformation Zone (LLETZ)/Loop Electrosurgical Excision Procedure (LEEP) • Laser cone biopsy • Cold knife cone biopsy • Hysterectomy (in cases of co-existing uterine conditions such as fibroids) Annual follow-up with Pap smears following treatment of precancerous lesions. MANAGEMENT (2)
  • 20.
  • 21. CONCLUSION Cervical/Pap smear is a useful screening tool to control the most common gynaecological cancer among women in Nigeria.
  • 22. REFERENCES 1. Cervical Screening: Overview, Human Papillomavirus, Papanicolaou Test. 2021 Aug 22 [cited 2022 Mar 10]; Available from: https://emedicine.medscape.com/article/1618870- overview 1. Gynaecology by ten teachers, 20E 1. HPV and premalignant disease of the cervix by Prof Anorlu