Ruptured solid pseudopapillary neoplasm in children: a 20-year single-center experience

Frontiers in Pediatrics 2026 Open access

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Authors: Suhyeon Ha, Soo-Min Jeong, Hyunhee Kwon, Namgoong Jung-Man
DOI: 10.3389/fped.2025.1738046
Cited by: 1
References: 18

Abstract

Purpose: Solid pseudopapillary neoplasm (SPN) is a rare pancreatic tumor with an excellent prognosis after resection. Tumor rupture is uncommon and may increase the risk of peritoneal spread, but data in children are extremely limited. This study evaluated clinicopathologic features, operative outcomes, and recurrence patterns in ruptured SPN in children over 20 years. Methods: We retrospectively reviewed seven children (

Fields of Study & Subjects

Pancreatic and Hepatic Oncology Research Pancreatitis Pathology and Treatment Gallbladder and Bile Duct Disorders

Publication details

Journal / source
Frontiers in Pediatrics
Publisher
Frontiers Media SA
Volume
13
Pages
1738046–1738046
Publication date
8 January 2026
Language
EN