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Solid Pseudopapillary Tumor of the Pancreas: a Rare Entity in Children

Abstract

Solid pseudopapillary tumors (SPTs) constitute 0.2 to 2.7% of non-endocrine primary tumors of the pancreas and comprise the majority (70%) of pediatric pancreatic neoplasms. These tumors are of unclear pathogenesis, low malignancy and favorable prognosis. Surgical resection offers an excellent chance for longterm survival, even in the presence of distant metastasis. The objective of this study is to review our experience in the management of SPT in a 12 years old girl at the pediatric hospital of the University hospital of Casablanca, in Morocco and provide an update on current management in pediatric population.

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Pseudopapillary solid tumour of the pancreas in paediatric age: description of a case report and review of the literature.

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PMID: 33895967 PMC: 9148352. DOI: 10.1007/s40477-021-00587-7.

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