Ectopic testis, unilateral
ICD-10 Q53.01 is a billable code used to indicate a diagnosis of ectopic testis, unilateral.
Ectopic testis, or ectopic testicular descent, refers to a condition where one testis fails to descend into the scrotum and instead is located in an abnormal position. This condition is classified as a congenital malformation of the genital organs and is often associated with other anomalies such as cryptorchidism. In unilateral ectopic testis, the affected testis may be found in various locations, including the inguinal canal, perineum, or thigh. The condition can lead to complications such as infertility, testicular torsion, and malignancy if not addressed. Diagnosis typically involves physical examination and imaging studies, while treatment often requires surgical intervention to reposition the testis into the scrotum. Ectopic testis is frequently seen in pediatric populations, and its management is crucial for normal sexual development and reproductive health.
Documentation must include detailed physical examination findings, imaging results, and any associated congenital anomalies.
Common scenarios include routine pediatric examinations where ectopic testis is discovered, or referrals for surgical intervention due to cryptorchidism.
Pediatric coders must be aware of the developmental implications of ectopic testis and the importance of timely intervention.
Genetic counseling notes should include family history, potential syndromic associations, and any chromosomal studies performed.
Scenarios may involve genetic evaluation for syndromes associated with ectopic testis, such as Klinefelter syndrome or Turner syndrome.
Genetic coders should consider the implications of chromosomal abnormalities that may present with genital malformations.
Used when surgical intervention is performed to reposition the ectopic testis.
Operative report detailing the procedure and findings.
Pediatric surgeons must document the specifics of the surgical approach and any complications.
Accurate coding of ectopic testis is crucial for appropriate management and treatment planning. It ensures that patients receive timely surgical intervention and helps in tracking congenital anomalies for research and epidemiological purposes.
