Pheochromocytoma of the urinary bladder--A case report

Vojnosanit Pregl. 2016 Jun;73(6):584-7. doi: 10.2298/vsp141115048m.

Abstract

Introduction: Pheochromocytoma of the urinary bladder is a rare tumor and presents less than 0.06% of all urinary bladder tumors.

Case report: We presented a 49-year-old female patient with a history of daily paroxysmal hypertension accompanied with flushing of the face and upper chest, palpitations and excessive sweating prior to micturition. Ultrasonography reported a 3 cm bladder wall tumor. The 131I-metaiodobenzylguanidine (131I-MIBG) scan showed a pathological isotope accumulation in the projection of the bladder. The patient underwent a partial cystectomy. One year following the operation the patient was normotensive and without recurrence.

Conclusion: The most efficient treatment option for bladder pheochromocytoma is surgical resection. The most important fact in the diagnostics is suspicion on this rare condition.

Publication types

  • Case Reports

MeSH terms

  • 3-Iodobenzylguanidine
  • Cystectomy
  • Female
  • Flushing / etiology
  • Humans
  • Hyperhidrosis / etiology
  • Hypertension / etiology
  • Middle Aged
  • Pheochromocytoma / complications
  • Pheochromocytoma / diagnosis*
  • Pheochromocytoma / surgery
  • Radiography
  • Radionuclide Imaging
  • Radiopharmaceuticals
  • Ultrasonography
  • Urinary Bladder / diagnostic imaging
  • Urinary Bladder Neoplasms / complications
  • Urinary Bladder Neoplasms / diagnosis*
  • Urinary Bladder Neoplasms / surgery

Substances

  • Radiopharmaceuticals
  • 3-Iodobenzylguanidine