Other congenital malformations of vulva
ICD-10 Q52.79 is a billable code used to indicate a diagnosis of other congenital malformations of vulva.
Congenital malformations of the vulva encompass a range of conditions that can affect the external female genitalia. These malformations may include abnormalities such as labial fusion, agenesis of the labia, or other structural anomalies that can impact the function and appearance of the vulva. Such conditions can arise from genetic factors, environmental influences, or developmental disruptions during fetal growth. In pediatric patients, these malformations may present with symptoms such as discomfort, difficulty with hygiene, or complications during puberty. Accurate diagnosis often requires a thorough clinical examination, imaging studies, and sometimes genetic testing to identify underlying chromosomal abnormalities. Treatment may involve surgical intervention, counseling, and ongoing monitoring to address any associated complications or psychosocial impacts. Understanding the full spectrum of congenital vulvar malformations is crucial for effective management and care planning.
Pediatric documentation should include detailed descriptions of the malformation, associated symptoms, and any interventions performed. Growth and developmental assessments are also important.
Common scenarios include a newborn presenting with ambiguous genitalia or a child with labial adhesions requiring surgical intervention.
Considerations include the psychosocial impact on the child and family, as well as the need for age-appropriate counseling.
Genetic documentation should include family history, results of genetic testing, and any syndromic associations with the malformation.
Scenarios may involve genetic counseling for families with a history of congenital malformations or syndromes associated with vulvar anomalies.
Genetic considerations include the potential for chromosomal abnormalities and the need for comprehensive genetic evaluation.
Used for surgical correction of labial fusion in pediatric patients.
Document the indication for surgery, pre-operative assessments, and post-operative care.
Pediatric surgical considerations include anesthesia risks and post-operative monitoring.
Documentation should include a detailed clinical description of the malformation, any associated symptoms, results from imaging or genetic testing, and a treatment plan outlining any surgical interventions.
