Primary ovarian solid pseudopapillary neoplasm associated with familial adenomatous polyposis

Authors

  • Alexandra McClaren Queen Elizabeth University Hospital, Glasgow, United Kingdom
  • Basil Syed University of Edinburgh, Old College, South Bridge, Edinburgh United Kingdom
  • Sheeba Syed Queen Elizabeth University Hospital, Glasgow, United Kingdom

DOI:

https://doi.org/10.59736/IJP.24.01.996

Keywords:

Pseudopapillary Neoplasm , Familial Adenomatous Polyposis

Abstract

Background: Solid pseudopapillary neoplasms (SPNs) are rare tumours, most often present in the pancreas. Extra-pancreatic SPNs are especially rare. Although FAP has not classically been associated with ovarian neoplasms, here we present the first documented case of a primary ovarian SPN in a patient with a known history of FAP.

Case presentation: We report a patient who developed ovarian SPN on follow-up for FAP.  A 25-year-old female with a background of FAP presented with a large abdominal mass, raised serum Ca125. Subsequently, the right salpingoopherectomy microscopically and immunocytochemically confirmed a Solid pseudopapillary neoplasm.

Conclusion: This case highlights awareness of possible occurrence of solid pseudopapillary neoplasm in the ovary in FAP patients. It is therefore important that SPNs are considered in the clinical and pathological differential diagnoses of tumors presenting in FAP patients.

Author Biography

  • Sheeba Syed, Queen Elizabeth University Hospital, Glasgow, United Kingdom

    Consultant Pathologist

References

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Published

2026-04-06

Issue

Section

Case Reports

How to Cite

1.
McClaren A, Syed B, Syed S. Primary ovarian solid pseudopapillary neoplasm associated with familial adenomatous polyposis. Int J Pathol [Internet]. 2026 Apr. 6 [cited 2026 Apr. 14];24(1):79-84. Available from: https://mail.jpathology.com/index.php/OJS/article/view/996