Archives of Clinical and Experimental Surgery (Mar 2016)

Metastatic pheochromocytoma in an 18-year-old

  • Ali Cadili,
  • Vanessa Falk,
  • Lucas Diebel,
  • Chris de Gara

DOI
https://doi.org/10.5455/aces.20140907061533
Journal volume & issue
Vol. 5, no. 1
pp. 48 – 51

Abstract

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Pheochromocytoma most commonly presents with a combination of headache, sweating, and hypertension. This case report reviews the case of a young male patient presenting with hypertensive crisis following administration of general anesthetics and who was subsequently diagnosed with malignant pheochromocytoma. Up to date, no reliable predictive factors for malignant pheochromocytoma have been established. This case emphasizes the need for a systematic approach to the hypertensive crisis and advantages of nuclear imaging to differentiate benign from malignant disease through detection of local invasion and distant metastases. [Arch Clin Exp Surg 2016; 5(1.000): 48-51]

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