ArticleMolecular and clinical oncology2016
Traumatic rupture of solid pseudopapillary tumors of the pancreas in children: A case report.
Article in Molecular and clinical oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 14 citations in OpenAlex.
- Massive calcified solid pseudopapillary neoplasm of the pancreatic head.Oncoscience · 2026Article
- Spontaneous Rupture of Solid Pseudopapillary Neoplasm of the Pancreas: A Case Report and Literature Review.Surgical case reports · 2025Article
- Spontaneous rupture of solid pseudopapillary epithelial neoplasm of pancreas with intraperitoneal haemorrhage.BMJ case reports · 2023Article
- Rare Solid Pancreatic Lesions on Cross-Sectional Imaging.Diagnostics (Basel, Switzerland) · 2023Review
- Solid Pseudo-papillary Neoplasia: A Rare Malignancy of the Pancreas.Journal of community hospital internal medicine perspectives · 2023Article
- Solid pseudopapillary neoplasm of the pancreas.World journal of hepatology · 2021Review
- Surgical Management of Solid Pseudopapillary Tumor of the Pancreas.JSLS : Journal of the Society of Laparoendoscopic SurgeonsArticle
- Solid Pseudopapillary Neoplasm of the Pancreatic Head in an 18-Year-Old Presenting with Chronic Intermittent Abdominal Pain: A Case Report.Case reports in oncologyArticle
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Authors and funding
6 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Solid pseudopapillary tumor (SPT) of the pancreas is a pathological entity rarely encountered in children. Despite its malignant characteristics, SPT has a favorable clinical prognosis. This tumor is more frequently observed in females and is commonly localized in the tail and body of the pancreas. This is the case report of a 9-year-old female patient who presented with severe abdominal pain of sudden onset and vomiting following blunt abdominal trauma. Upon physical examination, abdominal distension, tenderness and abdominal guarding were detected. Abdominal magnetic resonance imaging revealed a mass sized 8×9×12 cm in the pancreas, with hemorrhagic-necrotic areas, and abundant intra-abdominal fluid. Intra-abdominal exploration confirmed the presence of an abundant amount of intraperitoneal hemorrhagic fluid. A mass was identified, originating from the body and the tail of the pancreas, adherent to the mesentery of the colon and the hilum of the spleen, which had ruptured in its inferolateral side. The tumor was extirpated together with the spleen and the involved parts of the pancreas. Histopathological examination demonstrated a solid pseudopapillary tumor of pancreatic origin. The patient's postoperative course was uneventful, clinically as well as metabolically.
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