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Optimizing Care for Undescended Testicles in Children and Adolescents-Diagnosis, Management, and Outcomes: A
Marko Bašković1,2,3,4,5, Jana Buzuk1, Bianka Dujić1
1School of Medicine, Catholic University of Croatia, Ilica 242, 10000 Zagreb, Croatia.
Insights
Cryptorchidism, the failure of testes to descend, affects 1-9% of male infants. Early surgical correction (orchidopexy) before 12 months improves fertility and reduces risks of subfertility and malignancy.
Area of Science:
- Urology
- Pediatric Surgery
- Reproductive Endocrinology
Background:
- Cryptorchidism is the most common congenital anomaly of the male genitourinary system.
- It involves testes failing to descend into the scrotum, with varying locations (intra-abdominal, inguinal, ectopic).
- Associated factors include genetic, environmental, and syndromic influences.
Purpose of the Study:
- To summarize the current understanding of cryptorchidism's etiology, diagnosis, and management.
- To emphasize the importance of early intervention for optimal outcomes.
- To highlight long-term risks and surveillance needs.
Main Methods:
- Review of existing literature on cryptorchidism.
- Clinical examination and diagnostic imaging (ultrasound, MRI).
- Surgical exploration and orchidopexy as definitive treatment.
Main Results:
- Early orchidopexy (before 12 months) improves spermatogenic potential and fertility.
- Delayed or intra-abdominal testes increase risks of subfertility and testicular germ cell tumors.
- Hormonal therapy has limited efficacy and is not a primary treatment.
Conclusions:
- Timely diagnosis and surgical correction are crucial for minimizing long-term complications.
- A multidisciplinary approach combining surgery and surveillance is essential.
- Increased malignancy risk persists post-orchidopexy, necessitating lifelong monitoring.
Abstract:
Cryptorchidism is the most prevalent congenital anomaly of the male genitourinary tract, with an incidence of approximately 1 to 9 percent in full-term male infants, decreasing with age due to spontaneous descent. It encompasses testes that fail to descend into the scrotum, which may be intra-abdominal, inguinal, or ectopic, and can be associated with syndromic, genetic, or environmental factors. The descent process occurs in two phases: intra-abdominal, driven by gubernacular development and androgen-independent mechanisms, and inguinoscrotal, regulated by hormonal and mechanical factors including androgens and the gubernaculum. Clinically, cryptorchidism manifests as absent or hypoplastic scrotal testes, often with inguinal fullness. Palpation and physical examination are primary diagnostic tools, with imaging such as ultrasound or MRI reserved for specific cases. Surgical exploration remains the definitive diagnostic modality, especially for nonpalpable testes. Early referral, ideally before 12 months of age, is essential for timely orchidopexy, which aims to position the testes within the scrotum to reduce risks of torsion, trauma, subfertility, and malignancy. Hormonal therapy shows limited efficacy and is generally not recommended as a primary treatment modality. Long-term outcomes indicate that early orchidopexy improves spermatogenic potential and fertility. Men with a history of cryptorchidism exhibit elevated risks of subfertility and testicular germ cell tumors, with the risk being higher if surgical correction is delayed or if testes remain intra-abdominal. The increased malignancy risk persists even after orchidopexy, underscoring the importance of vigilant surveillance. Management strategies emphasize a multidisciplinary approach, combining surgical intervention with ongoing monitoring, to optimize functional and oncological outcomes. Early diagnosis, appropriate surgical treatment, and patient education are critical components in minimizing long-term complications associated with cryptorchidism.
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