Summary
Background
Solid pseudopapillary tumours, also known as Frantz’s tumours, are rare pancreatic lesions which usually occur in young 20–30 year-old women. They account for about 2% of all exocrine pancreatic tumours. They often present with vague abdominal pain and the diagnosis is frequently an incidental finding.
Methods
In this case series and narrative review, we attempt to update the current standpoint on primary pseudopapillary tumours. In this paper we present a case series of three subjects (2 females and 1 male) who were diagnosed with primary pseudopapillary tumours. Their treatment and follow-up is described in detail.
Results
These tumours will be discussed in the context of a literature review.
Conclusions
Surgical resection remains the primary method of treatment for this subtype of pancreatic tumours. The prognosis is excellent in patients who undergo resection.
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M. Portelli, S. Bozanic, D. Pisani, K. Cortis and J.-E. Abela declare that they have no competing interests.
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This article does not contain any studies with human participants or animals performed by any of the authors. Informed consent was obtained from all individual participants included in this case series. Copies of the consent forms are available for review from the Editor-in-Chief of this journal upon request.
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Portelli, M., Bozanic, S., Pisani, D. et al. Pseudopapillary tumours of the pancreas. Eur Surg 50, 189–194 (2018). https://doi.org/10.1007/s10353-018-0520-6
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DOI: https://doi.org/10.1007/s10353-018-0520-6