O&G Vivas · Gynaecological oncology — premalignant cervical disease
Colposcopy and treatment of CIN/CGIN — structured oral station (12 minutes)
FRANZCOG oral-format station on a high-grade squamous lesion at colposcopy: candidate performs the structured assessment, defends the ablation-vs-excision decision, counsels on the obstetric cost of excision, and manages glandular cytology. Scored against the eight published RANZCOG oral domains.
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Target exams
Station format
4 minutes reading, 12 minutes examination, 20 marks, global scoring. The eight published RANZCOG oral domains apply: history and examination; investigations and interpreting results; treatment and management; clinical knowledge; complex, urgent or unusual clinical presentations; rapport; respect; communication skills. You are marked on how you behave, not only what you know.[3]
Reveal the examiner script and model responses
Opening prompt — "Take me through your colposcopic assessment."
Model response: [3]
- "I perform a magnified assessment of the transformation zone after acetic acid, because most cervical cancers develop there. My first question is whether the squamocolumnar junction is fully visible — the IFCPC transformation zone type."
- "Here the junction is fully visible, so the colposcopy is satisfactory. I record the lesion site, size and worst feature — dense acetowhite change with abnormal vessels — and I take a directed biopsy before any destructive treatment, because histology is the standard."
Probe 1 — "The biopsy confirms CIN 3. Do you ablate or excise?"
- "Either is eligible here because the lesion is fully visible, the junction is seen, and invasion is excluded on cytology, colposcopy and biopsy. Because she wants children I would prefer excision with LLETZ to obtain histology and confirm complete excision, while being deliberate about depth."[2]
- State the ablation eligibility criteria out loud: whole lesion visible, SCJ fully seen (type 1 or 2), no suspicion of invasion, no glandular disease, concordant cytology and colposcopy with a biopsy excluding invasion.[3]
- "If the zone were type 3 — the junction not fully seen — I would not ablate, because lesions in the endocervical canal may be missed; I would sample the endocervix and excise."
Probe 2 — "She asks how this treatment might affect a future pregnancy."
Counsel with the specifics — this is a scored domain: [1]
- "Excision of the transformation zone is associated with adverse pregnancy outcomes. In the Kyrgiou meta-analysis, LLETZ raised the risk of preterm delivery — relative risk 1.70 — low birthweight 1.82, and premature rupture of the membranes 2.69; cold-knife conisation carried higher risks still."
- "The Athanasiou network meta-analysis confirmed that more radical excision carries more preterm-birth risk, while ablation probably does not increase preterm-birth risk."
- Acknowledge her concern, give the numbers plainly, and commit to minimising excision depth and to a clear follow-up plan.
Probe 3 — "Her cytology had shown possible glandular neoplasia of endocervical type instead, with a normal-looking colposcopy. What would change?"
- "Excision is essential. Among women referred with possible glandular neoplasia on cytology, 85.4% had significant pathology — AIS, invasive cancer or high-grade CIN — and AIS is a histological diagnosis, so colposcopy alone cannot rule it out and complete excision is required."[4]
- "I would never ablate suspected glandular disease; I would perform endocervical sampling and an excisional cone, and counsel that residual AIS is found even after clear margins — about 32% in one series — so surveillance continues and hysterectomy is recommended once fertility is no longer desired."[5]
Probe 4 — "She is frightened by the word 'precancer'. How do you respond?"
Demonstrate rapport, respect and communication out loud: [6]
- Move to her eye level, use her name, explain plainly: the abnormal cells are at a stage before cancer, the treatment removes them, and the outlook is excellent.
- Avoid jargon, acknowledge her fear, confirm she has understood, and arrange a clear follow-up plan and a point of contact.
Probe 5 — "What about HPV vaccination in all this?"
- "Vaccination prevents disease but does not treat it — she can still develop disease from non-vaccine HPV types or from infection acquired before vaccination, so she still needs screening."[6]
You have read the opening of this viva. The complete unit — every section and its primary-source references — is part of the Obstetrics & Gynaecology fellowship atlas.
References6Show ledgerHide ledger
- [1]Kyrgiou M, Koliopoulos G, Martin-Hirsch P, Arbyn M, Prendiville W, Paraskevaidis E Obstetric outcomes after conservative treatment for intraepithelial or early invasive cervical lesions: systematic review and meta-analysis Lancet, 2006.PMID 16473126
- [2]Athanasiou A, Veroniki AA, Efthimiou O, Kalliala I, Naci H, Bowden S, et al. Comparative effectiveness and risk of preterm birth of local treatments for cervical intraepithelial neoplasia and stage IA1 cervical cancer: a systematic review and network meta-analysis Lancet Oncol, 2022.PMID 35835138
- [3]Effah K, Tekpor E, Wormenor CM, Essel NOM Transformation zone types: a call for review of the IFCPC terminology to embrace practice in low-resource settings Ecancermedicalscience, 2023.PMID 38414959
- [4]Nikolopoulos M, Athanasias P, Godfrey MAL, Nikolopoulos K, Maheshwari MK Cervical glandular neoplasia referrals and the diagnosis of adenocarcinoma in situ: Correlating cytology, colposcopy findings, and clinical outcomes Cytopathology, 2021.PMID 34181788
- [5]Bell SG, Peng K, Kobernik EK, Miller ME, Lieberman R, Saunders NA, et al. Fertility and Pregnancy Outcomes After Conservative Management of Adenocarcinoma In Situ of the Cervix J Low Genit Tract Dis, 2021.PMID 34369435
- [6]Boldeanu L, Assani MZ, Boldeanu MV, Siloși I, Manolea MM, Văduva CC, et al. Cervical Cancer in the Era of HPV: Translating Molecular Mechanisms into Preventive Public Health Action Int J Mol Sci, 2025.PMID 40943384