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Pheochromocytoma Presenting as Testicular Pain: An Unusual Case Report

  • Jinal K Patel
  • , Varun Reddy
  • , Gauthier L Stepman
  • , Debra Angelo
  • , Johnathan Frunzi
  • HCA Healthcare

Research output: Contribution to journalArticlepeer-review

Abstract

Pheochromocytoma (PCC) is a rare catecholamine-secreting tumor that arises from chromaffin cells of the adrenal medulla which are derived from the neural crest. This report illustrates a 51-year-old Caucasian male with a history of hypertension diagnosed two years ago who presented to the hospital due to acute onset of right testicular pain of 3-day duration. Laboratory results and imaging revealed a presumptive diagnosis of PCC. The patient had undergone robot-assisted laparoscopic right adrenalectomy 14 days after being diagnosed with PCC due to perioperative management with phenoxybenzamine. The final pathology report revealed a PCC. At follow-up two weeks after discharge, the patient reported complete resolution of his testicular pain.

Original languageAmerican English
JournalEndocrinology
StatePublished - Apr 15 2021

Keywords

  • Pheochromocytoma
  • Neuroendocrine tumors
  • Adrenalectomy
  • Endocrine surgical procedures

Disciplines

  • Endocrine System Diseases
  • Endocrinology, Diabetes, and Metabolism
  • Neoplasms
  • Surgical Procedures, Operative

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