Polyorchidism: a rare entity as an incidental finding

Authors

  • Miguel Correia da Silva Centro Hospitalar Universitário de São João https://orcid.org/0000-0001-5392-2808
  • Sara Fernandes Serviço de Cirurgia Pediátrica, Centro Hospitalar Universitário de São João - Porto, Portugal https://orcid.org/0000-0002-0638-6958
  • Ana Teresa Vilares Serviço de Radiologia, Centro Hospitalar Universitário de São João - Porto, Portugal https://orcid.org/0000-0001-7375-491X
  • Sílvia Costa Dias Serviço de Radiologia, Centro Hospitalar Universitário de São João - Porto, Portugal
  • Miguel Campos Serviço de Cirurgia Pediátrica, Centro Hospitalar Universitário de São João - Porto, Portugal https://orcid.org/0000-0001-8580-3539
  • António José Madureira Serviço de Radiologia, Centro Hospitalar Universitário de São João - Porto, Portugal https://orcid.org/0000-0003-2490-1447

DOI:

https://doi.org/10.25748/arp.27611

Abstract

Polyorchidism is a rare condition. Its diagnosis is mostly incidental and its management is still a matter of debate. Herein we report a case of triorchidism and its management.

A 6-year-old boy presented with asymptomatic left scrotal swelling. Scrotal ultrasound confirmed hydrocele and described a supernumerary testis on the left side, along with bilateral testicular microlithiasis. Intraoperative examination of the scrotal content confirmed triorchidism: two testicular masses sharing the same epididymis and vas deferens. Preservation of both units was decided and considering the free movement between them and the inherent risk of torsion, a fixation suture was accomplished. The postoperative recovery was uneventful.

According to the scarce reports on literature, since testicular drainage into a shared vas deferens was confirmed, no resection was pursued. Considering the increased risk of malignancy, an annual ultrasound follow-up was recommended.

Downloads

Published

2023-04-30

Issue

Section

Clinical Cases