Published online Jan 15, 2025. doi: 10.4251/wjgo.v17.i1.101477
Revised: October 3, 2024
Accepted: October 18, 2024
Published online: January 15, 2025
Processing time: 87 Days and 17.4 Hours
Core Tip: This editorial analyzes a 22-year nationwide survey on pediatric pancreatic tumors in Japan. The predominance of solid pseudopapillary neoplasms and their younger age of onset contrast sharply with Western data, highlighting the need for population-specific approaches. Centralizing healthcare services could address the limited experience with these rare tumors observed at many institutions. The commentary also advocates for precision medicine, innovative care delivery models, and international collaborative studies on genetic and environmental factors across diverse populations. These insights could significantly improve the diagnosis, treatment, and management of pediatric pancreatic and other rare neoplasms globally, stimulating further research and clinical advancements.
