Evidence map›Paper›PMID 40110276›Full record

ArticleAnnals of medicine and surgery (2012)2025

Spontaneous ruptured solid pseudopapillary tumor of pancreas: a rare condition identified in a patient presenting with features of shock.

Shishir Devkota, Kshitiz Acharya, Navin Poudel, Aron Shrestha, Abhishek Bhattarai, Prasan B S Kansakar

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Article in Annals of medicine and surgery (2012), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Shishir DevkotaDepartment of General Surgery, Tribhuvan University Teaching Hospital, Kathmandu, Nepal.
Kshitiz AcharyaMaharajgunj Medical Campus, Tribhuvan University Institute of Medicine, Kathmandu, Nepal.
Navin PoudelMaharajgunj Medical Campus, Tribhuvan University Institute of Medicine, Kathmandu, Nepal.
Aron ShresthaMaharajgunj Medical Campus, Tribhuvan University Institute of Medicine, Kathmandu, Nepal.
Abhishek BhattaraiDepartment of General Surgery, Tribhuvan University Teaching Hospital, Kathmandu, Nepal.
Prasan B S KansakarDepartment of General Surgery, Tribhuvan University Teaching Hospital, Kathmandu, Nepal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Solid pseudopapillary tumor of pancreas are rare benign tumors of pancreas, that typically affects the young women. They are usually asymptomatic or minimally symptomatic, and are usually diagnosed by different imaging modalities. Case presentation: We herein present a case of solid pseudopapillary tumor of pancreas in an 18-year-old female patient who presented to our emergency department with features of shock following its spontaneous rupture. Imaging showed features suggestive of solid pseudopapillary tumor of pancreas, and she was managed by exploratory laparotomy following initial resuscitation. Discussion: Solid pseudopapillary tumors of pancreas are one of the rare exocrine pancreatic tumors. Their origin is not exactly clear, the most accepted theory states that these tumors originate from the multipotent primordial cells. Preoperative diagnosis can be made showing features distinct from other pancreatic solid/cystic neoplasms. Surgical management is the preferred treatment modality in these tumors. Conclusion: These are rare entities of pancreas, and may present with vague abdominal symptoms. Sometimes, these tumors may undergo spontaneous rupture, presenting with features of shock.

Indexed as

case reportpancreatic tumorshocksolid pseudopapillary tumor of pancreasspontaneous rupture

Identifiers

PMID40110276
PMCPMC11918701

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