İstanbul Medical Journal (Dec 2015)

Delayed Paraganglioma Diagnosis: A Case Report and Literature Update

  • Şamil Ecirli,
  • Mustafa Korkmaz,
  • Orkide Kutlu,
  • Cevdet Duran,
  • Mustafa Önder Gören,
  • Abdullah Sakin

DOI
https://doi.org/10.5152/imj.2015.92668
Journal volume & issue
Vol. 16, no. 4
pp. 162 – 164

Abstract

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Paragangliomas are rare catecholamine secreting neuroendocrine tumors arising from extra-adrenal autonomic ganglia. Almost all sympathetic paragangliomas secrete norepinephrine and present with hypertension, headache, sweating, and tachycardia episodes similar to pheochromocytoma. Parasympathetic paragangliomas of which localized along the glossopharyngeal/vagal nerve through the neck and skull base are usually nonfunctional 80%–90%, and create a clinic with mass effect. Herein, we report a patient who had hypertensive crisis and pulmonary edemas several times, diagnosed as paraganglioma. Consequently, implanted cardioverter defibrillator was diagnosed as paraganglioma.

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