ArticleThe American journal of case reports2020
A Rare Case of Large Solid Pseudopapillary Tumor in a Child
Article in The American journal of case reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed, 6 citations in OpenAlex.
- Extremely large solid pseudopapillary neoplasm of the pancreas.Clinical journal of gastroenterology · 2026Article
- Pseudopapillary solid tumour of the pancreas in paediatric age: description of a case report and review of the literature.Journal of ultrasound · 2022Review
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
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Abstract
BACKGROUND Solid pseudopapillary tumor (SPT) is a rare disease with low-grade malignancy potential of the pancreas. SPT accounts from 0.13% to 2.7% of all exocrine pancreatic tumors. We report an unusual case with a large solid pseudopapillary tumor that was diagnosed and treated in our pediatric hospital. CASE REPORT A 15-year-old girl was incidentally found to have an abdominal mass on ultrasound examination. Computed tomography (CT) scans showed a well-defined tumor that was raised in part of the tail and body of the pancreas. The tumor size at greatest diameter was 18.2 cm. A mass excision was performed to remove the whole tumor, and the histopathological findings confirmed SPT without evidence of malignancy. CONCLUSIONS SPT is a rare disease that mostly affects young female patients. The clinical symptoms of this disease are unspecific. The prognosis of SPT is good, even in case of distant metastasis. Close follow-up is required to detect metastasis so the appropriate treatment method can be chosen.
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