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A case of pancreatic solid-pseudopapillary neoplasm with marked ossification
Kana Tajima1, Yoshiaki Kawaguchi2, Hiroyuki Ito3
1Department of Gastroenterology, Tokai University School of Medicine, 143 Shimo-Kasuya, Isehara, Kanagawa, 259-1193, Japan. tajikana@is.icc.u-tokai.ac.jp.
Clinical Journal of Gastroenterology
|July 21, 2015
Summary
A rare case of pancreatic solid-pseudopapillary neoplasm (SPN) with ossification was found in a young woman. This study details the imaging, surgical, and pathological findings of this unusual pancreatic tumor.
Area of Science:
- Gastroenterology
- Oncology
- Radiology
Background:
- Pancreatic solid-pseudopapillary neoplasms (SPNs) are rare tumors, typically affecting young women.
- Ossification within an SPN is an exceptionally uncommon finding, posing diagnostic challenges.
Purpose of the Study:
- To report a unique case of pancreatic SPN with ossification.
- To discuss the diagnostic modalities and histopathological features of this rare entity.
Main Methods:
- A case study of a 25-year-old female with an incidentally discovered pancreatic lesion.
- Diagnostic imaging included computed tomography (CT), magnetic resonance imaging (MRI), and endoscopic ultrasound.
- Surgical resection and histopathological examination with immunohistochemistry were performed.
Main Results:
- Imaging revealed a pancreatic body mass with significant ossification (calcification).
- Histopathology confirmed a solid-pseudopapillary neoplasm with ossification and positive α1-antitrypsin staining.
- The tumor measured approximately 20-25 mm and showed infiltration of surrounding tissue.
Conclusions:
- Pancreatic SPN with ossification is a rare but distinct clinicopathological entity.
- Multimodality imaging is crucial for suspecting SPN, especially with atypical features like ossification.
- Surgical resection remains the primary treatment for pancreatic SPN.

