Congenital pancreatic cyst
ICD-10 Q45.2 is a billable code used to indicate a diagnosis of congenital pancreatic cyst.
Congenital pancreatic cysts are fluid-filled sacs that develop in the pancreas during fetal development. These cysts can vary in size and may be solitary or multiple. They are often discovered incidentally during imaging studies for other conditions. While many congenital pancreatic cysts are asymptomatic, they can sometimes lead to complications such as abdominal pain, pancreatitis, or obstruction of the pancreatic duct. The exact etiology of these cysts is not fully understood, but they may be associated with genetic syndromes or other congenital anomalies. In pediatric patients, careful monitoring is essential to assess for any potential complications or changes in the cysts over time. Management may include surgical intervention if the cysts cause significant symptoms or complications. Understanding the implications of congenital pancreatic cysts is crucial for pediatricians and specialists in genetics, as they may be part of broader syndromic presentations that require comprehensive evaluation and management.
Detailed clinical notes including symptoms, imaging results, and management plans.
Pediatric patients presenting with abdominal pain or incidental findings on imaging.
Consideration of the child's growth and development in relation to the cyst.
Family history documentation and genetic testing results if applicable.
Patients with congenital pancreatic cysts as part of a genetic syndrome requiring counseling.
Assessment for syndromic associations and implications for family members.
Used when surgical intervention is required for symptomatic cysts.
Operative report detailing findings and interventions.
Pediatric surgical notes should emphasize congenital aspects.
Common symptoms may include abdominal pain, nausea, vomiting, or signs of pancreatitis. However, many cysts are asymptomatic and found incidentally during imaging.
