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 language | American English |
|---|---|
| Journal | Endocrinology |
| State | Published - 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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