Skip to main content
Annals of Ibadan Postgraduate Medicine logoLink to Annals of Ibadan Postgraduate Medicine
. 2015 Dec;13(2):108–109.

POLYCYSTIC OVARIES: A COMMON FEATURE IN TRANSVAGINAL SCANS OF GYNAECOLOGICAL PATIENTS

FA Bello 1, AO Odeku 2
PMCID: PMC4853876  PMID: 27162523

BACKGROUND

Polycystic ovaries (PCO) are described on ultrasound scan as the "presence of 12 or more follicles in each ovary measuring 2-9 mm in diameter, and/or increased ovarian volume (>10 ml)"1 . Polycystic ovarian syndrome (PCOS) or disease (PCOD) is diagnosed when polycystic ovaries are associated with chronic anovulation and clinical and/or biochemical androgen excess (typically featured as oligo-amenorrhoea and hirsutism/acne, respectively). The Rotterdam criteria1 for diagnosis require any two of the three features. Unilaterality does not affect diagnosis; neither does the location of the cysts in the ovary.

PCOS is associated with infertility, as well as obesity, insulin resistance and hyperinsulinaemia, leading to impaired glucose tolerance1. Obesity and hyperinsulinaemia individually result in increased androgen production1. In most women, management includes lifestyle modifications towards weight loss. Oral hypoglycaemic agents help to improve insulin sensitivity; some women start to have regular periods with the use of metformin only2. PCOS is a diagnosis of medical interest, as associations with important non-communicable diseases have been made-notably, the metabolic syndrome. This comprises: insulin resistance, obesity, hypertension and dyslipidaemia, which significantly increase the woman's risk of cardiovascular disease3. This makes the evaluation of PCOS in the study environment of a wider interest beyond infertility.

Prevalence of polycystic ovarian syndrome is up to 10-26% of reproductive age group women in the Western world4,5, but only 0.6% of reproductive age-group gynaecological cases was reported from Nigeria6. Polycystic ovaries (PCO) were seen on ultrasound scans in 33% of the previously referenced population in which 26% were diagnosed with PCOS5.

This study aimed to document the prevalence of polycystic ovaries amongst women who had gynaecological ultrasound scans at an ultrasound diagnostic centre in Ibadan, Nigeria.

METHODS

This was a retrospective review of 671 gynaecological transvaginal scans (TVS) performed over a year at a female-reproductive health ultrasound diagnostic centre in Ibadan, Nigeria. All obstetric TVSs were excluded. All scans were performed with a 5.0 MHz or 6.0 MHz transvaginal probe (Hitachi Aloka Medical Ltd., Tokyo, Japan and Chison Medical Imaging Co. Ltd., Wuxi City, Jiang Su Province, China, respectively). Probes were sheathed in lubricated latex condoms before use. Data were analysed with IBM SPSS Statistics 20 by simple frequencies and means.

RESULTS

One hundred and five clients had polycystic ovaries by the Rotterdam definition1; a proportion of 15.6%. Most of these clients were in the 20-29 years' age range, with a mean age of 27.6 ± 5.7 years. Infertility (37.1%) was the most common indication for the TVS, followed by oligo-amenorrhoea (29.6%). Table 1 shows the indications. Fifty-seven (54.3%) women had unilateral polycystic ovaries; the rest (45.7%) had bilateral. Data on hyperandrogenism were not collected, however, using the available features of the Rotterdam criteria (PCO morphology and oligo-amenorrhoea), at least 31 (29.5%) of these clients have PCOS.

Table 1:

Indications for gynaecological transvaginal scan

Indications No (%)

Amenorrhoea 8 (7.6)
Oligomenorrhoea 23 (22.0)
Infertility 39 (37.1)
Lower abdominal pain 6 (5.7)
Uterine/ovarian assessment 19 (18.1)
To rule out pregnancy 6 (5.7)
Dysfunction uterine bleeding 4 (3.8)

DISCUSSION

About a sixth of the women in this series had polycystic ovaries, while a third fulfilled the limited available criteria for PCOS. This indicates that the syndrome may be more common than was previously diagnosed in the study environment6. The significance of this is not known. A limitation of previous assessment might have been due to the use of the transabdominal ultrasound route, which is not as sensitive as the transvaginal probe for evaluating the pelvis; and particularly the ovary. This will suggest that PCO prevalence has not necessarily increased; but rather the sensitivity of the diagnostic measure improved. If, however, the prevalence did increase, it may be due to an association with an increase in obesity and impairment of glucose intolerance that is emerging in the study environment. Lifestyle changes have occurred over the years: modern occupations are more sedentary, more people have cars and therefore walk less, and there is a surge in availability of fast food outlets and increase in refined sugar in diet. Obesity is not the cause of PCOS, of course; however, simple obesity is also associated with insulin resistance, and can therefore initiate the cascade of hyperinsulinaemia, excess androgen production and anovulation7. It has been suggested that the presence of polycystic ovaries alone should alert clinicians to advise women to avoid weight gain, which causes a worsening of the syndrome and greater long term morbidity8.

The review identifies PCO morphology, which does not always translate into PCOS-its interpretation is thus limited. As a follow-up to this, the authors are currently prospectively evaluating associations of PCO, and it is hoped that this would contribute to the knowledge of the epidemiology in the study environment.

REFERENCES

  • 1.Rotterdam ESHRE/ASRM-Sponsored PCOS Consensus Workshop Group. Revised 2003 consensus on diagnostic criteria and long-term health risks related to polycystic ovary syndrome. Fertil Steril. 2004;81(1):19–25. doi: 10.1016/j.fertnstert.2003.10.004. [DOI] [PubMed] [Google Scholar]
  • 2.Legro RS, Arslanian SA, Ehrmann DA, et al. Endocrine Society. Diagnosis and Treatment of Polycystic Ovary Syndrome: An Endocrine Society Clinical Practice Guideline. J Clin Endocrinol Metab. 2013;98(12):4565–4592. doi: 10.1210/jc.2013-2350. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Sharpless JL. Polycystic Ovary Syndrome and the Metabolic Syndrome. Clin Diabetes. 2003;21(4):154–161. [Google Scholar]
  • 4.Cahill D. PCOS. BMJ Clin Evid. 2009;2009:1408. [PMC free article] [PubMed] [Google Scholar]
  • 5.Michelmore KF, Balen AH, Dunger DB, Vessey MP. Polycystic ovaries and associated clinical and biochemical features in young women. Clin Endocrinol. 1999;51(6):779–786. doi: 10.1046/j.1365-2265.1999.00886.x. [DOI] [PubMed] [Google Scholar]
  • 6.Ocheke AN, Musa J. An Audit of Diagnosis and Management of Polycystic Ovarian Syndrome. J Medicine Tropics. 2012;14(1):49–52. [Google Scholar]
  • 7.Wilkes S, Murdoch A. Obesity and female fertility: a primary care perspective. J Fam Plann Reprod Health Care. 2009;35(3):181–185. doi: 10.1783/147118909788707995. [DOI] [PubMed] [Google Scholar]
  • 8.Balen A, Homburg R, Franks S. Defining polycystic ovary syndrome. BMJ. 2009;338:a2968. doi: 10.1136/bmj.a2968. [DOI] [PubMed] [Google Scholar]

Articles from Annals of Ibadan Postgraduate Medicine are provided here courtesy of Association of Resident Doctors, University College Hospital, Ibadan, Nigeria

RESOURCES