Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate
ICD-10 Q55.4 is a billable code used to indicate a diagnosis of other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate.
Congenital malformations of the male reproductive system can significantly impact fertility and overall health. This code encompasses a variety of conditions affecting the vas deferens, epididymis, seminal vesicles, and prostate. Common congenital anomalies include agenesis or hypoplasia of these structures, which may lead to obstructive azoospermia or infertility. Other conditions may involve abnormal positioning or structural deformities that can complicate normal reproductive function. In pediatric patients, these malformations may present with symptoms such as urinary tract infections, abnormal genitalia, or issues with sexual development. Early diagnosis and intervention are crucial for managing these conditions, which may require a multidisciplinary approach involving urologists, endocrinologists, and geneticists to address both the physical and psychological aspects of care.
Detailed clinical notes describing the child's growth, development, and any associated symptoms or conditions.
Cases of cryptorchidism, hypospadias, or ambiguous genitalia requiring surgical intervention or hormonal therapy.
Pediatric coders must be aware of the developmental implications of these conditions and the importance of early intervention.
Genetic testing results, family history, and any syndromic associations must be documented to support the diagnosis.
Genetic counseling for families with a history of congenital malformations or chromosomal abnormalities.
Genetic coders should ensure that all relevant genetic syndromes are considered when coding.
Used for surgical correction of cryptorchidism in pediatric patients.
Surgical notes detailing the procedure and pre-operative assessments.
Urologists must document the specifics of the malformation and any associated conditions.
Surgical intervention for hypospadias in children.
Detailed operative reports and post-operative follow-up notes.
Pediatric surgeons should ensure accurate coding of the procedure and associated congenital conditions.
Common congenital malformations associated with Q55.4 include agenesis or hypoplasia of the vas deferens, epididymis, seminal vesicles, and prostate, which can lead to fertility issues and other complications.
