Intrapancreatic mass: A rare cause

Maximilian Sohn1, Martin Fuchs2, Helmut Rohrbach3

  • 1Department of General, Abdominal, Endocrine and Minimally Invasive Surgery, Bogenhausen Hospital, Munich City Hospital Ltd., München, Germany.

Insights

A rare pancreatic extraintestinal gastrointestinal stromal tumor (pEGIST) was identified in a patient. Surgical resection led to a favorable outcome with no recurrence observed during a 23-month follow-up period.

Area of Science:

  • Gastroenterology
  • Surgical Oncology
  • Pathology

Background:

  • Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal neoplasms of the gastrointestinal tract.
  • Extragastrointestinal GISTs (EGISTs) are rare, accounting for only 2-5% of all GISTs.
  • Pancreatic EGISTs are exceptionally rare, often presenting diagnostic challenges due to their location.

Observation:

  • A patient initially suspected of having pancreatic adenocarcinoma underwent surgical resection.
  • The surgical procedure involved an open left hemipancreatectomy and en bloc splenectomy.
  • Postoperative histopathological examination revealed the tumor to be a pancreatic extraintestinal gastrointestinal stromal tumor (pEGIST).

Findings:

  • The unexpected diagnosis of pEGIST was confirmed post-surgery.
  • The patient experienced an uncomplicated recovery following the surgical intervention.
  • A follow-up period of 23 months showed no evidence of tumor recurrence.

Implications:

  • This case highlights the importance of thorough histopathological evaluation for accurate diagnosis of pancreatic neoplasms.
  • Early detection and surgical management of pEGIST can lead to favorable patient outcomes.
  • Further research into the characteristics and management of rare pancreatic tumors like pEGIST is warranted.

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