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CASE REPORT
Atypical case of preterm ovarian hyperstimulation syndrome
  1. Michelle A Durst1,
  2. Brandy Wicklow2,3,
  3. Michael Narvey3,4
  1. 1University of Manitoba, Department of Paediatrics and Child Health, Winnipeg, Manitoba, Canada
  2. 2University of Manitoba, Department of Paediatrics and Child Health, Section of Paediatric Endocrinology, Winnipeg, Manitoba, Canada
  3. 3Children's Hospital Research Institute of Manitoba, Winnipeg, Manitoba, Canada
  4. 4University of Manitoba, Department of Paediatrics and Child Health, Section of Neonatology, Winnipeg, Manitoba, Canada
  1. Correspondence to Dr Michelle A Durst, mdurst{at}manitoba-physicians.ca

Summary

Preterm ovarian hyperstimulation syndrome is a rare syndrome in which preterm infant girls have hypogastric, upper leg and labial swelling accompanied by elevated serum oestradiol levels and ovarian follicular cysts on ultrasound. Our case is an infant born at 23 weeks gestational age who at 30 weeks postconceptional age (PCA) developed elevated 17-hydroxyprogesterone on her newborn screen with associated clitoromegaly and a ventral groove on the inferior aspect of the erectile tissue. An initial pelvic ultrasound at 32 weeks PCA demonstrated a normal appearing uterus, but the ovaries were not visualised. At 39 weeks PCA, follicular ovarian cysts were noted bilaterally (31×26×21 mm on left and 38×25×36 mm on right). Without treatment, oestradiol and testosterone levels began normalising by 42 weeks PCA. After this point, the right ovarian cysts had resolved and the left ovarian cyst continued to diminish in size.

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Footnotes

  • Contributors MN identified and managed the case in the NICU. BW was consulted for management of the case as a paediatric endocrinologist. MD was involved in the latter part of patient’s stay in the NICU as a resident. MN, BW and MD were involved in producing the final manuscript.

  • Competing interests None declared.

  • Patient consent Obtained.

  • Provenance and peer review Not commissioned; externally peer reviewed.