Eur J Pediatr Surg 2010; 20(1): 62-65
DOI: 10.1055/s-0029-1216343
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© Georg Thieme Verlag KG Stuttgart · New York

Solid Pseudopapillary Tumor of the Pancreas: Raising Awareness of a not so Rare Pancreatic Tumor Affecting Young Females

E. Yaacobi 1 , Z. Steiner 1 , I. Ashkenazi 2 , B. Kessel 3 , R. Alfici 2
  • 1Hillel Yaffe Medical Center, Pediatric Surgery Unit, Hadera, Israel
  • 2Hillel Yaffe Medical Center, Surgery B Department, Hadera, Israel
  • 3Hillel Yaffe Medical Center, Trauma Unit, Hadera, Israel
Further Information

Publication History

Publication Date:
22 June 2009 (online)

Introduction

Solid pseudopapillary tumor of the pancreas (SPT) is a low-grade malignant tumor, which is usually diagnosed in adolescent girls and young women [7]. It comprises 2–3% of all primary pancreatic tumors diagnosed. Few patients will develop lymphatic, hepatic and/or peritoneal metastases [2] [10] [12]. Accurate diagnosis of this unusual tumor is important, because the prognosis after surgical resection is excellent.

Between 2003 and 2006, 41 cases of primary pancreatic tumors were operated at Hillel Yaffe Medical Center (HYMC). Of these, three (7.3%) patients were found to suffer from SPT. We describe these cases here, highlighting important aspects in the management of this tumor, once thought to be rare.

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Correspondence

Dr. I. Ashkenazi

Hillel Yaffe Medical Center

Surgery B Department

POB 169

38100 Hadera

Israel

Phone: +972/4/630 47 61

Fax: +972/4/630 45 45

Email: i_ashkenazi@yahoo.com

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