A rare cause of primary amenorrhoea, the XY female with gonadal dysgenesis

BMJ Case Rep. 2015 Feb 9:2015:bcr2014206609. doi: 10.1136/bcr-2014-206609.

Abstract

Disorders of sexual development are conditions where sexual phenotype and genotype are discordant. Genetic sex is determined at conception as the ovum is fertilised by a spermatozoon that contains either an X or Y chromosome. A complex pathway determined by genes and hormones leads to gonadal differentiation into testis or ovary and promotes the development of internal and external genitalia. We present a case of an 18-year-old woman who presented with primary amenorrhoea. She was a virgin, and apart from hirsutism and overweight, had no complaints. Her family history was insignificant. The patient was tall and had underdeveloped breasts. Her blood results showed hypergonadotropic hypogonadism. A 46, XY genotype was detected with karyotype analysis. Ultrasound and MRI demonstrated the presence of a uterus, but no overt gonads. Laparoscopy was performed, with bilateral removal of streak ovaries.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Amenorrhea / diagnosis
  • Amenorrhea / etiology*
  • Diagnosis, Differential
  • Female
  • Gonadal Dysgenesis, 46,XY / complications*
  • Gonadal Dysgenesis, 46,XY / diagnosis
  • Humans
  • Karyotyping
  • Magnetic Resonance Imaging