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O&G VivasEarly pregnancy care

O&G Vivas · Early pregnancy care

Adnexal mass in early pregnancy — structured oral station (12 minutes)

FRANZCOG oral-format station on an adnexal mass in early pregnancy: IOTA characterisation, the tumour marker pitfall, the decidualised endometrioma as the great mimic, torsion recognition and management, and the consent numbers for non-obstetric surgery. Scored against the eight published RANZCOG oral domains.

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Target exams

FRANZCOGMRCOGABOG
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Target exams

FRANZCOGMRCOGABOG
Prompt
You are the early pregnancy registrar. A 30-year-old woman at 12 weeks gestation, conceived by IVF, is referred with a 7 cm right adnexal mass found at her dating scan. She has known endometriosis. She is currently asymptomatic. The examiner will ask you to characterise the mass, defend your investigative strategy, manage the natural history, recognise torsion, and counsel the woman about surgery if it becomes necessary.

Station format

4 minutes reading, 12 minutes examination, 20 marks, global scoring. The eight published RANZCOG oral domains apply to every station: history and examination; investigations and interpreting results; treatment/management; clinical knowledge; complex, urgent or unusual clinical presentations; rapport with patient, support person or colleague; respect; communication skills. You are being marked on how you behave, not only what you know. [1]

Reveal the examiner script and model responsesShowHide

Opening prompt — "How would you characterise this mass?"

Model response — say it in this order: [1][2]

  • "I would describe the mass in IOTA terminology — size in three dimensions, locularity, solid components, papillary projections, acoustic shadows, ascites and a colour Doppler score — and then apply the IOTA Simple Rules."
  • "The Simple Rules are five B features that predict benignity and five M features that predict malignancy. One or more M and no B means malignant; the reverse means benign; both or neither is inconclusive, and I would then use the ADNEX model or expert subjective assessment."
  • "In the Timmerman prospective validation of 1938 masses, the Simple Rules were conclusive in 77% and gave a sensitivity of 92% and specificity of 96%. Where inconclusive, expert subjective assessment outperformed the Risk of Malignancy Index."[1]

Probe 1 — "The registrar asks whether to send CA-125, AFP, hCG and inhibin."

  • "I would not routinely send a tumour marker panel in pregnancy. CA-125 exceeds the cut-off in up to 35% of normal pregnancies, highest in the first trimester — a mid-range value is non-informative."[7]
  • "I would trust the imaging. If I needed a second-line test, it would be non-contrast MRI — first-trimester MRI has not been associated with fetal harm in the Ray cohort, but gadolinium at any gestation has been associated with stillbirth, neonatal death and rheumatological outcomes."[8]

Probe 2 — "She has known endometriosis. The mass has papillary projections with flow."

  • "This is the classic decidualised endometrioma — producing papillary projections with flow that mimic the M features of malignancy. It is the great mimic in this topic."
  • "In the Barcroft pregnancy-specific IOTA two-step pilot of 291 pregnant women, decidualisation occurred in 31.1% of endometriomas and resolved in 89.5% by the first postnatal scan. ADNEX misclassified 34% of benign masses as malignant, over half of which were decidualised endometriomas."
  • "Management is to resist surgery, use expert subjective assessment and serial imaging, and rescan postnatally. I would not refer her to oncology on these features alone."[4]

Probe 3 — "She re-presents at 16 weeks with sudden severe right iliac fossa pain and vomiting."

  • "This is ovarian torsion until proven otherwise. The history and the known mass make the diagnosis; imaging is supportive but I would not delay theatre for it."
  • "Analgesia, IV access, bloods, nil by mouth, anaesthetic and theatre. Laparoscopic detorsion with ovarian conservation — a dusky torted ovary may still be viable, and oophorectomy is reserved for confirmed necrosis."
  • "In Dvash's cohort of torsion in pregnancy, live birth was 92.5% and preterm delivery 19.4%, the latter driven mainly by multiple pregnancy. Almost half of torsion cases in pregnancy follow IVF or ovulation induction."[5]

Probe 4 — "If she needs elective surgery, when and how?"

  • "Elective surgery belongs in the second trimester — after organogenesis and while access is still good. The counterweight is that necessary surgery is never delayed for gestational age; a torsion at 32 weeks still goes to theatre."
  • "Laparoscopy is preferred over laparotomy. In the Cagino meta-analysis, laparoscopy showed no significant increase in spontaneous abortion (OR 1.53, 95% CI 0.67 to 3.52) or preterm delivery (OR 0.95, 95% CI 0.47 to 1.89), with a shorter length of stay."[9]
  • "Technique: laparoscopy adapted to the gravid uterus — entry sited to avoid the uterus, low insufflation pressure, capnography, left lateral positioning, minimal uterine manipulation, and thromboprophylaxis."[9]

Probe 5 — "She asks whether the surgery will harm her baby."

  • "Surgery in pregnancy is generally safe — the attributable risk is low — but I would give her the absolute numbers. In the Balinskaite cohort of 6.5 million pregnancies, non-obstetric surgery was associated with one additional stillbirth per 287 operations, one additional preterm delivery per 31, one additional low-birthweight baby per 39, one additional caesarean per 25, and one additional long inpatient stay per 50."
  • "I would frame it honestly: the absolute risk to her pregnancy is small, and the operation is being done for a good reason — but these are the numbers."[6]

Probe 6 — "What if the mass had M features and ascites from the start?"

  • "Then this is no longer a watch-and-wait problem. I would refer to gynaecological oncology, stage with non-contrast MRI, and plan a multidisciplinary approach — exactly as I would outside pregnancy."
  • "The malignancy rate among adnexal masses that come to surgery in pregnancy is only around 1%, and the borderline ovarian tumour dominates in this age group. The plan would usually be fertility-sparing where feasible."[9][4]
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References9ShowHide
  1. [1]Timmerman D, Ameye L, Fischerova D, et al. Simple ultrasound rules to distinguish between benign and malignant adnexal masses before surgery: prospective validation by IOTA group. BMJ, 2010.PMID 21156740
  2. [2]Van Calster B, Van Hoorde K, Valentin L, et al. Evaluating the risk of ovarian cancer before surgery using the ADNEX model to differentiate between benign, borderline, early and advanced stage invasive, and secondary metastatic tumours: prospective multicentre diagnostic study. BMJ, 2014.PMID 25320247
  3. [3]Barreñada L, Ledger A, Dhiman P, et al. ADNEX risk prediction model for diagnosis of ovarian cancer: systematic review and meta-analysis of external validation studies. BMJ Med, 2024.PMID 38375077
  4. [4]Barcroft J, Pandrich M, Del Forno S, et al. Evaluating use of two-step International Ovarian Tumor Analysis strategy to classify adnexal masses identified in pregnancy: pilot study. Ultrasound Obstet Gynecol, 2024.PMID 38787921
  5. [5]Dvash S, Pekar M, Melcer Y, et al. Adnexal Torsion in Pregnancy Managed by Laparoscopy Is Associated with Favorable Obstetric Outcomes. J Minim Invasive Gynecol, 2020.PMID 31563614
  6. [6]Balinskaite V, Bottle A, Sodhi V, et al. The Risk of Adverse Pregnancy Outcomes Following Nonobstetric Surgery During Pregnancy: Estimates From a Retrospective Cohort Study of 6.5 Million Pregnancies. Ann Surg, 2017.PMID 27617856
  7. [7]Han SN, Lotgerink A, Gziri MM, et al. Physiologic variations of serum tumor markers in gynecological malignancies during pregnancy: a systematic review. BMC Med, 2012.PMID 22873292
  8. [8]Ray JG, Vermeulen MJ, Bharatha A, et al. Association Between MRI Exposure During Pregnancy and Fetal and Childhood Outcomes. JAMA, 2016.PMID 27599330
  9. [9]Cagino K, Li X, Thomas C, et al. Surgical Management of Adnexal Masses in Pregnancy: A Systematic Review and Meta-analysis. J Minim Invasive Gynecol, 2021.PMID 33515746
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