Other congenital malformations of bile ducts
ICD-10 Q44.5 is a billable code used to indicate a diagnosis of other congenital malformations of bile ducts.
Congenital malformations of the bile ducts encompass a range of structural anomalies that can significantly impact the digestive system. These malformations may include conditions such as biliary atresia, where the bile ducts are absent or blocked, leading to bile accumulation and liver damage. Other anomalies may involve cystic dilatation of the bile ducts or abnormal connections between the bile ducts and other structures. These conditions often present in infancy with symptoms such as jaundice, dark urine, pale stools, and poor weight gain. Diagnosis typically involves imaging studies such as ultrasound or MRI, and management may require surgical intervention to restore bile flow or liver transplantation in severe cases. Understanding the complexities of these congenital malformations is crucial for accurate coding and appropriate clinical management.
Detailed pediatric history including prenatal factors, birth history, and developmental milestones.
Infants presenting with jaundice, failure to thrive, or abdominal distension due to congenital bile duct anomalies.
Consideration of associated congenital conditions and the need for multidisciplinary management.
Genetic testing results, family history of congenital conditions, and any syndromic associations.
Cases where congenital malformations are part of a genetic syndrome, requiring genetic counseling.
Understanding the genetic basis of congenital malformations and implications for family planning.
Used in cases of gallbladder anomalies requiring surgical intervention.
Operative report detailing the procedure and indications.
Pediatric surgical considerations for congenital cases.
Common symptoms include jaundice, dark urine, pale stools, and poor weight gain in infants. These symptoms arise due to impaired bile flow and liver function.
