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Updated: Jun 20, 2026

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Published on: November 17, 2023
Polyorchidism: a meta-analysis
Robert Bergholz1, Katharina Wenke
1Department of Pediatric Surgery, UKE Medical School, Hamburg University, Altona Children's Hospital, Hamburg, Germany. robert@bergholz-berlin.de
Purpose:
Polyorchidism is an uncommon congenital anomaly. We systematically analyzed the literature due to the contradictory data regarding this condition.
Materials And Methods:
We conducted a database search and evaluated relevant articles for the appearance, comorbidities and complications of supernumerary testes. Only cases of polyorchidism confirmed by histological examination were included in the study.
Results:
We found 140 cases of polyorchidism. Triorchidism was the most common type, and 6 cases of 4 testes (4.3%) were reported. Most supernumerary testes (64%, chi-square p <0.001) were drained by a vas deferens. Median patient age at detection was 17 years. Left side demonstrated predominance (64.5%, chi-square p <0.001). Most cases were found during surgery for other symptoms including inguinal hernia, undescended testicle, testicular torsion and scrotal pain. Only 16% of patients complained of an accessory mass without any symptoms. Neoplasms were found in 9 cases (6.4%), of which 8 were malignant and 1 was benign. Data available for 7 malignomas (88%) revealed that all were in cryptorchid supernumerary testes.
Conclusions:
Polyorchidism is rare and is generally found during evaluation for other conditions such as inguinal hernia, undescended testis and testicular torsion. Cryptorchidism appears to be the most important risk factor for malignancy in patients with supernumerary testes. Thus, patients with nonscrotal supernumerary testes require appropriate counseling. The supernumerary testis is frequently drained by a vas deferens, implying a probable reproductive function. Decision for surgery, biopsy or orchiectomy should be based on concomitant symptoms, cryptorchidism or suspected malignancy. We provide a guideline for management based on a functional classification of polyorchidism.
Insights
Polyorchidism, a rare congenital condition, is often discovered incidentally during evaluations for other issues. Cryptorchidism (undescended testes) is a significant risk factor for malignancy in patients with supernumerary testes.
Area of Science:
- Urology
- Congenital Anomalies
- Surgical Pathology
Background:
- Polyorchidism, characterized by the presence of supernumerary testes, is an uncommon congenital anomaly.
- Existing literature presents contradictory data regarding its clinical presentation, comorbidities, and complications.
Purpose of the Study:
- To systematically analyze the existing literature on polyorchidism.
- To clarify the appearance, comorbidities, and complications associated with supernumerary testes.
Main Methods:
- A comprehensive database search was conducted to identify relevant studies.
- Inclusion criteria required polyorchidism cases to be confirmed by histological examination.
- Data extraction focused on the presentation, comorbidities, and complications of supernumerary testes.
Main Results:
- 140 cases of polyorchidism were identified, with triorchidism being the most common type.
- Supernumerary testes were predominantly found on the left side (64.5%) and often associated with inguinal hernia, undescended testicle, testicular torsion, or scrotal pain.
- Neoplasms occurred in 6.4% of cases, with 88% of these malignancies arising in cryptorchid supernumerary testes.
Conclusions:
- Polyorchidism is a rare condition typically diagnosed during investigations for other urological issues.
- Cryptorchidism is identified as the primary risk factor for malignancy in supernumerary testes, necessitating careful management and counseling.
- The frequent presence of a vas deferens suggests potential reproductive function, influencing management decisions regarding surgery, biopsy, or orchiectomy.
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