Gynecology and Minimally Invasive Therapy (Jan 2021)

46 xy ovotesticular disorder: A rare case report with review of literature

  • Bhati Meenal,
  • Gothwal Meenakshi,
  • Singh Pratibha,
  • Yadav Garima,
  • Kathuria Priyanka,
  • Elhence Poonam

DOI
https://doi.org/10.4103/GMIT.GMIT_107_19
Journal volume & issue
Vol. 10, no. 3
pp. 171 – 173

Abstract

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Ovotesticular disorder represents 10% of cases of disorder of sex development characterized by the presence of both ovarian and testicular tissue in the same individual, with karyotype 46 XY being a rare sex chromosomal abnormality. We report the case of a 16-year-old person, who is reared as female, with a complaint of primary amenorrhea along with lack of secondary sexual characteristics, karyotype 46 XY. Prophylactic bilateral gonadectomy was done, and histopathological examination of bilateral gonads revealed ovarian stroma with a few Sertoli cell line tubules suggestive of bilateral ovotestis; hence, we concluded and framed our diagnosis of ovotesticular disorder.

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