Giant Esophageal GIST: Diagnostic and Therapeutic Challenge - Case Report

Chirurgia (Bucharest, Romania : 1990)
|July 10, 2015
PubMed

Insights

This case study details a rare esophageal gastrointestinal stromal tumor (GIST) successfully removed surgically. The patient is now undergoing targeted therapy with imatinib mesylate due to a high risk of relapse.

Area of Science:

  • Gastroenterology
  • Oncology
  • Thoracic Surgery

Background:

  • Gastrointestinal stromal tumors (GIST) are rare mesenchymal neoplasms, accounting for less than 1% of digestive tract tumors.
  • Esophageal GIST represent a very small subset of these rare tumors, posing unique diagnostic and therapeutic challenges.

Observation:

  • A 51-year-old female presented with fatigue, leading to the discovery of a bulky posterior mediastinal mass.
  • Imaging revealed a mediastinal tumor deviating the thoracic esophagus without causing dysphagia or respiratory compromise.

Findings:

  • Surgical exploration via thoracotomy confirmed and completely excised the esophageal GIST.
  • Histopathology confirmed the diagnosis, but fragmented tumor removal indicated a high risk of recurrence.

Implications:

  • Complete surgical resection is the primary treatment for esophageal GIST.
  • Adjuvant therapy with tyrosine kinase inhibitors, such as imatinib mesylate, is crucial for managing high-risk cases and preventing relapse.

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