Unveiling a Rare Pancreatic Tumor in Bangladesh: Solid PseudopapillaryTumor

DOI: https://doi.org/10.47648/jmsr.2023.v3502.05

Nadeed Masih1 , H.A Nazmul Hakim2

Abstract

Solid Pseudopapillary Tumors are rare pancreaticneoplasms first identified as Hammoudi or Franztumors, later classified by the WHO as SPTs in1996. These tumors primarily affect young non-Caucasian women, with a male-to-female ratioof 1:11. Surgical excision remains the standardtreatment. Solid Pseudopapillary Tumors (SPTs)within the pancreas are rare, accounting for less than3% of pancreatic neoplasms. They predominantlyoccur in young women and are characterized by lowmalignant potential with high surgical cure rates.This report details the case of a 14-year-old girlin Bangladesh undergoing a successful Whipple’sprocedure for an SPT.

This case report aims to share our unique findings, which may contribute to understanding and knowledge of this rare medical condition and its treatment options.

Keywords:


  1. In course Trainee, Department of Surgery

    Dhaka Medical College Hospital, Dhaka

  2. Associate Professor, Department of Surgery

    Dhaka Medical College Hospital, Dhaka


Volume 35, Number 2 July 2023
Page: 28-31