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RD7.{1,6} | Imaging in Obstetrics, Gynecology and Breast Care — Practice Quiz
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A 22-year-old woman with oligomenorrhoea and clinical hyperandrogenism undergoes transvaginal ultrasound. The radiologist reports each ovary contains 24 small peripherally arranged follicles measuring 2–9 mm, with an ovarian volume of 9 mL, using a modern high-frequency transducer. Which single statement best integrates these findings into her diagnosis?
Correct. With modern high-frequency transducers the follicle-number threshold for polycystic ovarian morphology has been revised upward to ≥20 follicles (2–9 mm) per ovary; ovarian volume >10 mL is an alternative, not a mandatory, criterion. Either suffices for the morphological component, which is only ONE of the three Rotterdam criteria.
Modern high-frequency transducer threshold for PCOM is ≥20 follicles per ovary (older/Rotterdam 2003 used ≥12); ovarian volume >10 mL is an alternative criterion. Morphology is one of three Rotterdam criteria.
Polycystic ovarian morphology is met by ≥20 follicles (2–9 mm) per ovary on a modern transducer OR ovarian volume >10 mL; morphology is just one of three Rotterdam criteria and does not by itself confirm PCOS.
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A regularly menstruating, asymptomatic 25-year-old has a pelvic ultrasound for an unrelated reason that incidentally shows 22 follicles in one ovary. She has no hyperandrogenism. How should this finding be integrated into her care?
Correct. Rotterdam requires any TWO of three criteria (oligo/anovulation, hyperandrogenism, polycystic ovarian morphology). A polycystic-appearing ovary in a woman with regular cycles and no hyperandrogenism is an isolated finding, not a diagnosis.
Rotterdam = any 2 of 3 (oligo/anovulation, hyperandrogenism, PCOM). Imaging is supportive, never standalone diagnostic.
The scan does not diagnose PCOS by itself; Rotterdam needs any two of three criteria. An isolated polycystic morphology in an asymptomatic, regularly cycling woman is not PCOS.
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A 28-year-old woman with a positive pregnancy test, 6 weeks amenorrhoea, and right iliac fossa pain has a transvaginal ultrasound showing an empty uterus. Her serum beta-hCG is 3200 IU/L. Which interpretation best integrates these findings?
Correct. With beta-hCG of 3200 IU/L (above the ~1500–2000 IU/L discriminatory zone) an intrauterine gestational sac should be visible. An empty uterus at this level is an ectopic until proven otherwise.
Empty uterus + beta-hCG above discriminatory zone (~1500–2000 IU/L) = ectopic until proven otherwise. Avoid ionising imaging in pregnancy; TVS is first-line.
Read the TVS against the beta-hCG. An empty uterus with hCG ABOVE the discriminatory zone (~1500–2000 IU/L) is an ectopic until proven otherwise — not reassuring.
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During evaluation of suspected ectopic pregnancy, the sonographer reports a small fluid collection within the endometrial cavity. Which feature most reliably distinguishes a true gestational sac from a pseudosac?
Correct. A true intrauterine gestational sac is eccentrically embedded in the decidua (double decidual sign) and may contain a yolk sac or fetal pole. A pseudosac is a central cavity fluid collection that follows the cavity shape and lacks these features.
True sac: eccentric, double decidual sign, may contain yolk sac/fetal pole. Pseudosac: central cavity collection, no yolk sac — do not call it an intrauterine pregnancy.
A true sac is eccentric within the decidua with a double decidual sign / yolk sac / fetal pole; a pseudosac is a central, featureless cavity collection. Mistaking a pseudosac for a true sac is a classic trap.
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A subfertile couple is being investigated. The female partner needs assessment of tubal patency and wishes to avoid ionising radiation. Which imaging approach best matches the factor being tested?
Correct. HyCoSy assesses tubal patency using ultrasound contrast and avoids ionising radiation, making it the radiation-free alternative to HSG. TVS assesses ovarian reserve, ovulation and the cavity but not tubal patency directly.
Tubal patency: HSG (follicular phase, day 6–10) or radiation-free HyCoSy. TVS assesses ovarian reserve/ovulation/uterine cavity.
Match the test to the factor. Tubal patency = HSG or its radiation-free alternative HyCoSy. TVS assesses ovarian reserve/ovulation/cavity, not patency.
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An HSG is planned for a woman being investigated for infertility. To maximise diagnostic value and safety, when in the menstrual cycle should the study be performed?
Correct. HSG is performed in the follicular phase (about day 6–10), after bleeding has stopped and before ovulation, so that an early pregnancy is not inadvertently exposed to ionising radiation.
HSG timing: follicular phase, day 6–10 — post-menstrual and pre-ovulatory to avoid radiation to an early pregnancy.
HSG is a follicular-phase study (day 6–10): after menses, before ovulation, to avoid irradiating a possible early pregnancy.
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A 32-year-old woman presents with a palpable breast lump. Her breasts are clinically dense and she is concerned about radiation. Which imaging modality is the appropriate first-line investigation of the lump?
Correct. Ultrasound characterises focal lumps and is first-line in young women and in dense breasts, where mammographic sensitivity falls; it also uses no ionising radiation. Mammography screens asymptomatic and older breasts.
Lump in young/dense breast → ultrasound first-line (radiation-free, better in dense tissue). Mammography is the screening tool for asymptomatic/older breasts.
Mammography screens; ultrasound characterises and is first-line for a lump in a young woman with dense breasts. It is also radiation-free.
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A screening mammogram in a 52-year-old woman is reported as BI-RADS 4 with a cluster of pleomorphic microcalcifications. How should this category be integrated into her management?
Correct. BI-RADS 4 is a suspicious category warranting tissue diagnosis. Imaging is one limb of the triple assessment (clinical examination + imaging + pathology); a suspicious image must be confirmed by biopsy, not treated as proven cancer.
BI-RADS scale 0–6: 0=incomplete, 1=negative, 2=benign, 3=probably benign (short interval follow-up), 4=suspicious (biopsy), 5=highly suggestive of malignancy (biopsy), 6=known cancer. Triple assessment = exam + imaging + pathology.
BI-RADS 4 = suspicious → biopsy. It is not benign (2), not proven malignancy (6), and not incomplete (0). Triple assessment integrates clinical exam, imaging and pathology.
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