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DOI: 10.1055/s-0045-1812057
Whole Body Fluoro-Deoxy-Glucose Positron Emission Tomography in Pediatric Solid Pseudopapillary Epithelial Neoplasm
Autoren
Abstract
Solid pseudopapillary epithelial neoplasm (SPEN) is a rare pancreatic tumor primarily affecting adolescent girls and young women. While generally indolent, SPEN can exhibit locally aggressive behavior or distant metastases. Accurate preoperative characterization is essential for optimal management.
Introduction
Solid pseudopapillary epithelial neoplasm (SPEN) is a rare pancreatic tumor primarily affecting adolescent girls and young women[1] [2] with a female-to-male ratio of 9:1. Less than 10% of SPEN cases occur in males, and these cases may present with distinct characteristics, such as being more locally invasive and aggressive compared with female patients.
Imaging plays a crucial role in its diagnosis and management, with conventional modalities like ultrasound, CT, and MRI providing morphological details. However, fluoro-deoxy-glucose (FDG) PET-CT offers additional functional insights by assessing the tumor's metabolic activity.[3] While SPEN typically demonstrates low to moderate FDG uptake, cases with aggressive features may exhibit increased metabolism.[4] [5] Here, we present a case highlighting the role of FDG PET-CT in evaluating SPEN, aiding in diagnosis, surgical planning, and disease monitoring.
Case
A 9-year-old boy presented with complaints of yellowish discoloration of the conjunctiva for the last 3 weeks. There was a history of intermittent abdominal pain with generalized itching. There was no history of fever, nausea, vomiting, or significant weight loss. There was no history of any other significant medical conditions, abdominal surgeries, or chronic illnesses. There was no known history of similar complaints in the past. The family history was noncontributory.
He was evaluated at a local hospital for the above complaints, with an ultrasound showing a 4.7 cm × 4.5 cm × 3.9 cm well-defined, heterogeneous, predominantly solid echogenic lesion in the pancreatic head, externally indenting the common bile duct (CBD), leading to upstream biliary dilatation.
He was referred for a whole body FDG PET-CT scan, which showed a mildly hypermetabolic (SUV max 2.6), well-defined heterogeneously enhancing soft tissue density lesion in the pancreatic head indenting the ampulla of Vater and CBD with dilatation of the cystic duct and common hepatic duct and bilateral intrahepatic biliary radicular dilatation ([Figs. 1] and [2]).




Because of localized disease with no aggressive behavior or distant metastasis, the patient underwent a Whipple's pancreaticoduodenectomy with complete resection of the tumor.
Discussion
SPEN of the pancreas are rare pancreatic tumors described by the WHO as low-grade malignant tumors. They tend to affect young women in the second or third decade of life and rarely affect children or men.[6] Due to their indolent nature, SPENs are most frequently discovered incidentally on physical examination or imaging for other reasons. An alternating solid and pseudopapillary architecture is characteristic of these tumors, which makes prompt radiological detection possible. Though SPENs are considered to have a relatively favorable prognosis, they have garnered attention in recent years due to an apparent increase in incidence. This study has also demonstrates a risk of metastasis or recurrence following surgical resection, emphasizing the need for close follow-up postoperatively.[2] [5]
Conclusion
FDG PET-CT serves as a valuable imaging modality in pediatric SPEN, aiding in tumor characterization, treatment planning, and detection of aggressive disease. Further studies are needed to establish standardized metabolic parameters for risk stratification and prognosis.
Conflict of Interest
None declared.
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References
- 1 WHO Classification of Tumours Editorial Board. Digestive System Tumours. 5th ed.. IARC Press; 2019
- 2 Papavramidis T, Papavramidis S. Solid pseudopapillary tumors of the pancreas: review of 718 patients reported in English literature. J Am Coll Surg 2005; 200 (06) 965-972
- 3 Zhang J, Wang J, Zhao J. et al. Clinical value of 18F-FDG PET/CT in the diagnosis of solid pseudopapillary neoplasms of the pancreas. Clin Nucl Med 2013; 38 (07) e285-e290
- 4 Zhou Y, Yang Y, Xia L. et al. Diagnostic value of FDG PET/CT in solid pseudopapillary neoplasms of the pancreas: a meta-analysis. Medicine (Baltimore) 2020; 99 (32) e21645
- 5 Choi JY, Kim MJ, Kim JH. et al. Solid pseudopapillary tumor of the pancreas: typical and atypical manifestations. AJR Am J Roentgenol 2006; 187 (02) W178-86
- 6 Crespo-Sánchez MD, Lira-Treviño JA, Treviño-Garza C. et al. Solid pseudopapillary neoplasm in children and adolescents: a case series and review of the literature. J Pediatr Surg 2020; 55 (02) 343-347
Address for correspondence
Publikationsverlauf
Artikel online veröffentlicht:
14. Oktober 2025
© 2025. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)
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References
- 1 WHO Classification of Tumours Editorial Board. Digestive System Tumours. 5th ed.. IARC Press; 2019
- 2 Papavramidis T, Papavramidis S. Solid pseudopapillary tumors of the pancreas: review of 718 patients reported in English literature. J Am Coll Surg 2005; 200 (06) 965-972
- 3 Zhang J, Wang J, Zhao J. et al. Clinical value of 18F-FDG PET/CT in the diagnosis of solid pseudopapillary neoplasms of the pancreas. Clin Nucl Med 2013; 38 (07) e285-e290
- 4 Zhou Y, Yang Y, Xia L. et al. Diagnostic value of FDG PET/CT in solid pseudopapillary neoplasms of the pancreas: a meta-analysis. Medicine (Baltimore) 2020; 99 (32) e21645
- 5 Choi JY, Kim MJ, Kim JH. et al. Solid pseudopapillary tumor of the pancreas: typical and atypical manifestations. AJR Am J Roentgenol 2006; 187 (02) W178-86
- 6 Crespo-Sánchez MD, Lira-Treviño JA, Treviño-Garza C. et al. Solid pseudopapillary neoplasm in children and adolescents: a case series and review of the literature. J Pediatr Surg 2020; 55 (02) 343-347





