Other congenital malformations of liver
ICD-10 Q44.79 is a billable code used to indicate a diagnosis of other congenital malformations of liver.
Congenital malformations of the liver encompass a variety of structural abnormalities that can significantly impact liver function and overall health. These malformations may include conditions such as biliary atresia, hepatic cysts, and vascular malformations. In pediatric patients, these conditions often present with symptoms such as jaundice, abdominal distension, and failure to thrive. Diagnosis typically involves imaging studies such as ultrasound or MRI, and may require liver biopsy for definitive diagnosis. Management strategies vary depending on the specific malformation and may include surgical interventions, medical management, and close monitoring. Understanding the interplay between congenital liver malformations and other digestive system anomalies, such as esophageal atresia, Hirschsprung disease, and gastroschisis, is crucial, as these conditions can co-occur and complicate clinical management.
Pediatric documentation must include growth parameters, developmental milestones, and specific symptoms related to liver function.
Common scenarios include a newborn presenting with jaundice and abdominal distension, requiring evaluation for biliary atresia.
Accurate coding requires understanding the implications of liver malformations on overall health and potential for multi-organ involvement.
Genetic documentation should include family history, genetic testing results, and any syndromic associations with liver malformations.
Scenarios may involve genetic counseling for families with a history of congenital liver disease.
Consideration of chromosomal abnormalities that may predispose to liver malformations is essential for accurate coding.
Used for definitive diagnosis of liver malformations.
Documentation must include indication for biopsy and results.
Pediatric considerations include sedation protocols and monitoring.
Common congenital liver malformations include biliary atresia, hepatic cysts, and vascular malformations. Each condition has distinct clinical presentations and management strategies.
