ArticleCase reports in surgery2026
Beyond the Expected: A Case-Based Exploration and Literature Review on the Rare Evolution of Pseudomyxoma Peritonei From a Side-Branch Intraductal Papillary Mucinous Neoplasm.
Article in Case reports in surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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1 citing paper in PubMed.
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4 authors.
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Abstract
Objectives: We present a case of a ruptured side-branch intraductal papillary mucinous neoplasm (IPMN) who was found to have pseudomyxoma peritonei (PMP) with a deposit of acellular mucin in the pelvis. Case Presentation: The patient is a 65-year-old female who initially presented to care with intermittent right upper quadrant pain and fullness. Preoperative imaging demonstrated a large cystic mass in the pancreatic tail, and, therefore, she was taken to the operating room for a distal pancreatectomy and splenectomy. Intraoperatively, she was found to have two distinct deposits of acellular mucin. Both deposits were nonadherent to the surrounding tissue and removed. Results: The patient recovered postoperatively without incident. She will be surveilled postoperatively with serial computed tomography. Conclusion: PMP arising from an IPMN of the pancreas is a rare and potentially devastating complication of the disease. Given the complexity of these cases, a multidisciplinary discussion for ongoing management is essential, and these cases are best managed at centers with significant experience in the management of PMP from other sources.
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