Adnexal Torsion Due to Borderline Mucinous Tumor of the Gonad in a Prepubertal Girl with Mixed Gonadal Dysgenesis (45,X/46,XY) and a Turner Phenotype

J Pediatr Adolesc Gynecol. 2022 Aug;35(4):492-495. doi: 10.1016/j.jpag.2022.01.002. Epub 2022 Jan 16.

Abstract

Background: Turner syndrome (TS) is a sex chromosome condition characterized by complete or partial loss of the X chromosome. Patients with mixed gonadal dysgenesis (45,X/46,XY) and a Turner phenotype are predisposed to gonadoblastoma with malignant transformation.

Case: We present the case of a TS patient with 45,X/46,XY with 2 episodes of left adnexal torsion (AT). Biopsies during detorsion showed benign mucinous cystadenoma. Pathology following bilateral gonadectomy revealed a left gonad with mucinous borderline tumor and right gonad with gonadoblastoma, both of which have malignant potential.

Summary and conclusion: Gonadectomy is recommended in XY gonadal dysgenesis to decrease risk of malignant transformation from gonadoblastoma. Although rare in pediatric patients, ovarian malignancies have been identified among AT cases. To our knowledge, we present the first case of AT due to borderline ovarian mucinous tumor of the ovary and contralateral gonadoblastoma in a patient with mixed gonadal dysgenesis (45,X/46,XY) and a Turner phenotype.

Keywords: Adnexal torsion; Gonadoblastoma; Malignant risk; Mixed gonadal dysgenesis; Mucinous borderline tumor; Ovarian torsion; Premenarchal; Turner syndrome; Turner syndrome with Y chromosome.

Publication types

  • Case Reports

MeSH terms

  • Female
  • Gonadal Dysgenesis*
  • Gonadal Dysgenesis, 46,XY*
  • Gonadal Dysgenesis, Mixed*
  • Gonadoblastoma* / complications
  • Gonadoblastoma* / genetics
  • Gonadoblastoma* / surgery
  • Gonads / pathology
  • Humans
  • Ovarian Neoplasms* / complications
  • Ovarian Neoplasms* / genetics
  • Ovarian Neoplasms* / surgery
  • Ovarian Torsion
  • Phenotype
  • Turner Syndrome* / complications
  • Turner Syndrome* / genetics