Paraganglioma in the posterior mediastinum: a case report

BMC Cardiovasc Disord. 2020 Nov 23;20(1):492. doi: 10.1186/s12872-020-01752-2.

Abstract

Background: Paragangliomas are tumors that arise from extra-adrenal chromaffin cells. Herein, we present a rare case of a functional paraganglioma in the posterior mediastinum.

Case presentation: A 36-year-old man presented with paroxysms of chest pain and headache. At presentation, the patient's blood pressure was 190/120 mmHg. Chest computed tomography and magnetic resonance imaging revealed a left paravertebral mass in the posterior mediastinum. 123I-metaiodobenzylguanidine scanning revealed focally high tracer uptake in the left paravertebral area. The metanephrine level in the urine was elevated, confirming a rare, catecholamine-producing, functional paraganglioma in the posterior mediastinum. Before surgery, the patient was prepared by orally administering α- and β-adrenergic blockers. The mass was then resected via a lateral thoracotomy. The metanephrine level in urine was normal 24 h after surgery.

Conclusions: Paragangliomas in the posterior mediastinum are very rare, but more than half of all cases are functional. The associated symptoms are curable with complete resection, and long-term follow-up for recurrence is important.

Keywords: Mediastinum; Paraganglioma; Pheochromocytoma.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Chest Pain / etiology
  • Headache / etiology
  • Humans
  • Hypertension / etiology
  • Male
  • Mediastinal Neoplasms* / complications
  • Mediastinal Neoplasms* / diagnosis
  • Mediastinal Neoplasms* / surgery
  • Paraganglioma, Extra-Adrenal* / complications
  • Paraganglioma, Extra-Adrenal* / diagnosis
  • Paraganglioma, Extra-Adrenal* / surgery
  • Thoracotomy
  • Treatment Outcome