Bilateral inguinal testes
ICD-10 Q53.212 is a billable code used to indicate a diagnosis of bilateral inguinal testes.
Bilateral inguinal testes, also known as bilateral inguinal cryptorchidism, is a congenital condition where both testes fail to descend into the scrotum and are located in the inguinal canal. This condition is often diagnosed during a physical examination in infancy or early childhood. The testes may be palpable in the inguinal canal, but they are not in their normal anatomical position. The failure of descent can be attributed to various factors, including hormonal imbalances, anatomical abnormalities, or genetic predispositions. If left untreated, bilateral inguinal testes can lead to complications such as infertility, testicular torsion, and an increased risk of testicular cancer. Surgical intervention, typically via orchidopexy, is the standard treatment to reposition the testes into the scrotum. Early diagnosis and management are crucial for optimal outcomes, and pediatricians often collaborate with urologists for comprehensive care.
Detailed physical examination findings, including testicular location and size, and any associated anomalies.
Infants presenting with undescended testes during routine check-ups, referrals for surgical intervention.
Consideration of the child's age and developmental milestones when planning surgical intervention.
Family history of cryptorchidism or other congenital anomalies, genetic testing results if applicable.
Genetic counseling for families with a history of congenital malformations, evaluation for syndromic associations.
Awareness of chromosomal abnormalities that may present with cryptorchidism, such as Klinefelter syndrome.
Performed to correct bilateral inguinal testes.
Operative report detailing the procedure and findings.
Pediatric urologists should ensure accurate coding of the procedure in relation to the diagnosis.
Accurate coding of bilateral inguinal testes is crucial for appropriate treatment planning, monitoring for associated conditions, and ensuring proper reimbursement for surgical interventions. It also aids in the collection of data for research and public health initiatives related to congenital anomalies.
