Other specified congenital malformations of male genital organs
ICD-10 Q55.8 is a billable code used to indicate a diagnosis of other specified congenital malformations of male genital organs.
Congenital malformations of male genital organs encompass a variety of conditions that can affect the development and function of the genitalia. This includes hypospadias, where the urethral opening is located on the underside of the penis rather than at the tip, and cryptorchidism, which is characterized by undescended testicles. Ambiguous genitalia, a condition where the external genitalia do not have a clear male or female appearance, can also fall under this category. Uterine malformations, while primarily affecting females, can be relevant in cases of intersex conditions or disorders of sexual development. These malformations can lead to complications such as urinary tract infections, fertility issues, and psychosocial challenges. Accurate coding is essential for appropriate management and treatment planning, as well as for research and epidemiological studies.
Detailed descriptions of physical examinations, growth patterns, and developmental milestones are crucial. Documentation should also include any surgical interventions or referrals to specialists.
Common scenarios include newborn assessments revealing hypospadias or cryptorchidism, and follow-up visits for surgical correction.
Pediatric coders must be aware of the age-specific implications of these conditions and the potential for long-term follow-up.
Genetic testing results, family history, and any syndromic associations should be documented thoroughly to support the diagnosis.
Scenarios may include genetic counseling for families with a history of congenital malformations or ambiguous genitalia.
Genetic coders should consider the implications of chromosomal abnormalities that may accompany these malformations.
Used when a patient with hypospadias undergoes surgical correction.
Operative reports detailing the procedure and any complications.
Pediatric urologists typically perform these procedures.
Documentation should include a detailed description of the malformation, any associated conditions, and the treatment plan. Surgical reports and genetic evaluations are also important.
