Conservative Management of Intrascrotal Polyorchidism in a 14‐Year‐Old Boy: A Case Report and Review of the Current Literature
Year: 2025
Type: article
Study design: Case Report
Abstract: Polyorchidism, or supernumerary testes (SNTs), is a rare congenital condition, management of which remains debated, particularly in paediatric cases with other concomitant features. We report a case of intrascrotal polyorchidism in a 14-year-old boy managed surgically due to parental preference and the need for histological confirmation. The patient presented with a 2-week history of painless heaviness in the scrotum. Physical examination and Doppler ultrasonography revealed a 1.8 cm mass fused to the inferior pole of the left testicle with associated Grade 1 varicocele, hydrocele and testicular appendix. Although MRI of the scrotum was initially offered, the family declined in favour of timely histological confirmation. Surgical exploration confirmed a fused supernumerary testicle and a biopsy showed normal spermatogenesis; this was consistent with Type A3 triorchidism. The patient had no complications or recurrence of symptoms at 12-month follow-up. This case highlights the use of surgical exploration in selected intrascrotal polyorchidism cases where imaging can be inconclusive or histological confirmation is required. Parental concerns and long-term reassurance may also reasonably influence management decisions.
Source: Case Reports in Urology
DOI: 10.1155/criu/5258413
Institutions: National and Kapodistrian University of Athens, Chelsea and Westminster Hospital NHS Foundation Trust, West Middlesex University Hospital, University General Hospital Attikon, Imperial College London, Penteli General Children's Hospital, University Hospital of Basel, University College London
Language: English
Subfield: Surgery
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $790
OpenAlex ID: W4414101648
