Clinical Features and Management of Pancreatic Solid Pseudopapillary Tumor

Author:

Tsukamoto Masayo1,Hashimoto Daisuke1,Chikamoto Akira1,Abe Shinya1,Ohmuraya Masaki2,Baba Hideo1

Affiliation:

1. Department of Gastroenterological Surgery

2. Institute of Resource Development and Analysis, Kumamoto University Graduate School of Medical Sciences, Japan

Abstract

Solid pseudopapillary tumor (SPT) is a rare pancreatic tumor with low malignant potential. Between February 2006 and May 2013, six patients were affected by SPT. Two patients were male and four were female. Median age of the patients was 31.5 years (range, 13 to 47 years). One patient was preoperatively diagnosed by an endoscopic ultrasound-guided fine-needle aspiration biopsy. Pancreaticoduodenectomy was performed in two and distal pancreatectomy was done in four. One operation of those was laparoscopic distal pancreatectomy. In this series, recurrence or distant metastasis was not reported and successful outcome was achieved in all patients. In conclusion, whereas diagnosis of SPT is difficult, it can be diagnosed by endoscopic ultrasound-guided fine-needle aspiration biopsy preoperatively. It should be treated by surgery, and laparoscopic operation can be considered.

Publisher

SAGE Publications

Subject

General Medicine

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Unusual Pancreatic Tumors;Shackelford's Surgery of the Alimentary Tract, 2 Volume Set;2019

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