A Potentially Malignant Giant Esophageal Paraganglioma

Ann Thorac Surg. 2019 Dec;108(6):e349-e351. doi: 10.1016/j.athoracsur.2019.03.106. Epub 2019 May 8.

Abstract

Paragangliomas are rare neuroendocrine tumors derived from extraadrenal autonomic paraganglia, which may secrete catecholamines. They are potentially metastatic and require very long-term follow-up. Esophageal paragangliomas are extremely rare and present a diagnostic challenge. Lack of clinical suspicion and unrecognized catecholamine hypersecretion may lead to hemodynamic instabilities during surgery. Two patients with esophageal paragangliomas were previously reported. We report a 39-year-old man with a giant high-risk esophageal paraganglioma who underwent a hybrid minimally invasive 3-hole esophagectomy.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Deglutition Disorders / diagnosis
  • Deglutition Disorders / etiology
  • Endoscopy, Digestive System / methods*
  • Esophageal Neoplasms / diagnostic imaging
  • Esophageal Neoplasms / pathology*
  • Esophageal Neoplasms / surgery*
  • Esophagectomy / methods*
  • Esophagoscopy / methods
  • Follow-Up Studies
  • Humans
  • Israel
  • Male
  • Minimally Invasive Surgical Procedures / methods
  • Neoplasm Invasiveness / pathology
  • Neoplasm Staging
  • Paraganglioma / diagnostic imaging
  • Paraganglioma / pathology*
  • Paraganglioma / surgery*
  • Rare Diseases
  • Treatment Outcome