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Robotic Central Pancreatectomy with Roux-en-Y Pancreaticojejunostomy
Published on: November 20, 2021
Pancreatic masses in children: a single-center experience over two decades
Joyce J L H McRae1, Humza Thobani2, Marla A Sacks3
1Division of Pediatric Surgery, Loma Linda University Children's Hospital, Loma Linda, CA, USA.
Insights
Pediatric pancreatic tumors are rare but treatable with surgery. Outcomes depend on early diagnosis and absence of metastatic disease, with excellent short-term surgical results.
Area of Science:
- Pediatric Oncology
- Surgical Oncology
- Gastroenterology
Background:
- Pancreatic masses in children are exceptionally rare, leading to limited clinical data and diagnostic challenges.
- Solid Pseudopapillary tumors are a common type of pediatric pancreatic tumor with a generally favorable prognosis after resection.
- Current data suggests surgical management is safe and effective for pediatric pancreatic tumors, particularly in the absence of aggressive histology or metastatic disease.
Purpose of the Study:
- To describe the clinical presentation, course, and outcomes of pediatric pancreatic tumors.
- To analyze surgical interventions and quality improvement measures for pediatric pancreatic tumor resections.
- To provide insights into the management and outcomes of five distinct pediatric pancreatic tumor types.
Main Methods:
- Retrospective analysis of pediatric patients diagnosed with pancreatic masses between 2003 and 2022.
- Inclusion of data on demographics, clinical presentation, workup, management, morbidity, and mortality.
- Review of the National Surgical Quality Improvement Program - Pediatric (NSQIP-P) database for surgical outcomes.
Main Results:
- Seventeen pediatric patients were identified with diagnoses including solid pseudopapillary tumors, gastrinoma, rhabdomyosarcoma, pancreatoblastoma, and insulinoma.
- Twelve patients underwent surgical intervention (pancreaticoduodenectomy, distal pancreatectomy), with all surviving at last contact.
- Three deaths occurred, exclusively due to complications from metastatic disease; 30-day postoperative outcomes in the NSQIP-P dataset were excellent with no mortalities.
Conclusions:
- Pediatric pancreatic tumors amenable to surgical resection demonstrate adequate long-term survival.
- Short-term outcomes are generally excellent and are primarily influenced by the presence of metastatic disease at diagnosis.
Abstract:
Pancreatic masses are extremely rare in pediatric patients, with limited data available. This lack of data makes the diagnosis and management of these tumors in children extremely challenging. Therefore, we aimed to describe the presentations, clinical course, and outcomes of children with pancreatic tumors at our center. A retrospective analysis was performed of all pediatric patients diagnosed with pancreatic masses between 2003 and 2022 in an academic freestanding children's hospital. Data including demographics, clinical presentation, workup, management, and subsequent morbidity and mortality were collected and aggregated. Furthermore, we reviewed cases of pancreatic tumor resections in the National Surgical Quality Improvement Program - Pediatric (NSQIP-P) database to identify common adverse outcomes and measures for quality improvement. In total, 17 patients were identified at our institution. Diagnoses included solid pseudopapillary (n = 9), gastrinoma (n = 1), rhabdomyosarcoma (n = 2), pancreatoblastoma (n = 2), and insulinoma (n = 1). Two patients did not have a histopathologic diagnosis and were excluded from subsequent analysis. Overall, 12 patients underwent surgical intervention, with the most common procedures being pancreaticoduodenectomy and distal pancreatectomy, and all 12 were known to be alive at last contact. There were 3 deaths, all due to complications related to metastatic disease. Furthermore, 30-day postoperative outcomes in the NSQIP-P dataset for pancreatic surgeries in pediatric patients are excellent, with negligible morbidity and no mortalities after the index surgery.
Conclusions:
Children with pancreatic tumors amenable to surgical resection appear to have adequate long-term survival. Short-term outcomes at diagnosis are excellent and mainly appear to be influenced by the presence of metastatic disease at initial presentation.
What Is Known:
• Pancreatic masses are a rare entity in children with limited data on their presentation, management and surgical outcomes. • Solid Pseudopapillary tumors are one of the most common pancreatic tumors in children with a fair prognosis after surgical intervention.
What Is New:
• Surgical management of pediatric patients with pancreatic tumors is safe and effective in patients who do not have aggressive tumor types or metastatic disease. • Our case series provides a notable cohort of these pancreatic tumors with insight into the presentation, management and outcomes of five of these tumor types.
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