Pseudopapilar Solid Tumor of Pancreas, as a Finding in Pediatric Patient

Case Report

Austin Pediatr. 2016; 3(5): 1047.

Pseudopapilar Solid Tumor of Pancreas, as a Finding in Pediatric Patient

Delgado YS*, Azuela OC, Quinto AG, Zepeda NC and Viana EH

General Mexican Hospital, ¨Dr. Eduardo Liceaga, Mexico

*Corresponding author: Sánchez Delgado Y, General Mexican Hospital ¨Dr. Eduardo Liceaga, Mexico

Received: November 08, 2016; Accepted: December 19, 2016; Published: December 21, 2016

Introduction

The pseudopapillary solid tumor, predominantly in young women in the third decade of life. It represents less than 1% of all pancreatic neoplasms [1] is also called Frantz-Gruber tumor was first described in 1959. The anatomy and histological elements include solid, cystic and pseudopapillary components; as well as being producers of mucin, present nonspecific clinical symptoms so the diagnosis is a finding against the persistent vague abdominal symptoms; however, described capsule ruptured acute peritonitis [2]. Hemoperitoneum and malignant potential of 14%. Preoperative diagnosis may be referred to as pancreatic pseudo cysts in patients with no history or risk factors for pancreatitis with normal serum amylase and a solid component of a cystic cavity without communication between the cyst and pancreatic ducts [3]. La surgical resection is performed pancreatoduodenectomy if the lesion is at the level of head-neck or distal pancreatectomy with splenectomy should be in the queue. Greater than 90% at 5 years, survival about 15% of patients develop metastatic disease to the liver, peritoneum and lymph nodes [4,5].

Purpose

Describe the incidental finding of a solid tumor pseudopapillary as abdominal tumor.

Methods

Was reported a case of abdominal tumor in the Pediatric General Surgery General Hospital of Mexico.

Clinical Presentation

Female patient 17 years of age having increased volume in the right upper quadrant of 6 months of evolution, which is progressive up to 10x10cm, after normal pregnancy. Referred early satiety, postprandial nausea and occasional vomiting, denies and weight loss. No chronic degenerative history, exposure to organic dusts or previous pictures of pancreatitis. Physical examination: Abdomen with tumor located in hypochondrium and right flank of 15x15x15 cm, indurated, defined, painless, motionless, well-defined edges, without vascular compromise, no evidence of peritoneal irritation. Laboratory and images reported (Figure 1 and Figure 2): 1.99 alpha-fetoprotein, carcinoembryonic antigen 1.29, beta fraction of chorionic gonadotrophin 0.23. Pancreatoduodenectomy was performed classically finding as tumor pancreatic head solid aspect of 20x20 cm surgical finding no evidence of metastasis, firm and loose adhesions, through unidentifiable Wirsung, cystic artery 10x1 mm, cistico of 10x3 mm, coledoco 6mm, root mesentery with no evidence of tumor. Figure 3 pathology results: pseudopapillary solid tumor in the pancreatic head (Figure 4). In the postoperative period, the patient has adequate clinical evolution, without evidence of bleeding, controlled pancreatic fistula presented with obstructive jaundice pattern, which was resolved with percutaneous catheter placement, he was discharged without complications.