Iatreia (Apr 2016)

Hypertension secondary to paraganglioma: case report and review of the literature

  • Rubio-Marín, Andrea Constanza,
  • Orjuela, Alba Dayana,
  • Rascovsky, Melissa,
  • Rosselli, Diego

DOI
https://doi.org/10.17533/udea.iatreia.v29n2a09
Journal volume & issue
Vol. 29, no. 2
pp. 206 – 217

Abstract

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We report the case of a 25 year-old man with a history of transient stroke during adolescence, and longstanding uncontrolled hypertension who presented with palpitations, diaphoresis and headache. He was diagnosed with a paraaortic paraganglioma associated with catecholamine hypersecretion, confirmed by histopathology. There was complete resolution of the symptoms after removal of the tumor. Paraganglioma, a rare extra-adrenal tumor, derived from chromaffin cells, should be considered in the diagnosis of secondary hypertension. We performed a literature review of paraganglioma cases with catecholamine hypersecretion, and associated hypertension.

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