Short-term results of duodenum-preserving pancreatic head resection for solid pseudopapillary neoplasm in children at the National Children's Hospital

Objective: To evaluate the results of duodenum-preserving pancreatic head resection for treating solid pseudopapillary neoplasm (SPN) of the pancreas in children at the National Children's Hospital. Methods: A descriptive, retrospective study of 11 patients diagnosed with pancreatic SPN and treated surgically at the National Children's Hospital from May 2022 to May 2024. Results: The average age of diagnosis in children was 10.9 years (range: 8-15 years), predominantly affecting female patients (81.8%). The main clinical symptoms were epigastric and left hypochondrial pain (81.8%). The average tumor size was 51.3 mm (range: 2.6-10 cm). Computed tomography (CT) imaging revealed a predominantly mixed structure in 9 out of 11 patients (81.8%). All patients underwent duodenum-preserving pancreatic head resection, with no severe intraoperative or postoperative complications. Conclusion: SPN is a rare pancreatic tumor with low malignancy, minimal invasiveness, and low rates of metastasis and recurrence. Thus, surgery is a safe and effective treatment method for children, with a low complication rate.

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Publication Details

Journal
Journal of Health Sciences
Published
2024-08-29
DOI
https://doi.org/10.59070/jhs010924035
Primary Topic
Pancreatic and Hepatic Oncology Research
Type
article
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article

Short-term results of duodenum-preserving pancreatic head resection for solid pseudopapillary neoplasm in children at the National Children's Hospital

Minh Ngoc Le Vu
Journal of Health Sciences
Pancreatic and Hepatic Oncology Research
article

Short-term results of duodenum-preserving pancreatic head resection for solid pseudopapillary neoplasm in children at the National Children's Hospital

Minh Ngoc Le Vu
article en

Abstract

Objective: To evaluate the results of duodenum-preserving pancreatic head resection for treating solid pseudopapillary neoplasm (SPN) of the pancreas in children at the National Children's Hospital. Methods: A descriptive, retrospective study of 11 patients diagnosed with pancreatic SPN and treated surgically at the National Children's Hospital from May 2022 to May 2024. Results: The average age of diagnosis in children was 10.9 years (range: 8-15 years), predominantly affecting female patients (81.8%). The main clinical symptoms were epigastric and left hypochondrial pain (81.8%). The average tumor size was 51.3 mm (range: 2.6-10 cm). Computed tomography (CT) imaging revealed a predominantly mixed structure in 9 out of 11 patients (81.8%). All patients underwent duodenum-preserving pancreatic head resection, with no severe intraoperative or postoperative complications. Conclusion: SPN is a rare pancreatic tumor with low malignancy, minimal invasiveness, and low rates of metastasis and recurrence. Thus, surgery is a safe and effective treatment method for children, with a low complication rate.

Journal of Health SciencesVol. 2(3)
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Pancreatic and Hepatic Oncology Research
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