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Bladder paraganglioma: Case report and review of the literature

  • Laura Pérez Barón (masterstudent)
  • , Nicolas Guerrero Acosta (Correspondent Author)
  • , Guillermo Granados González (masterstudent)
  • , Juan Carlos Aldana (Fourth Autor)
  • , Rodolfo Mantilla Espinosa (Fifth Author)
  • , German Andrés Carmona (undergradstudent)
  • Universidad de la Sabana
  • Clinica Shaio

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Pheochromocytoma is a tumor that originates from the chromaffin cells of the adrenal medulla and is responsible for the production of catecholamines. However, when it occurs outside the adrenal glands, it is called a paraganglioma and accounts for 10%-15% of cases. In this report, we present the case of a 27-year-old male patient with a history of hypertension, who presented hematuria and dizziness on urination with a diagnosis of bladder paraganglioma. Contrast-enhanced computed tomography revealed the presence of a bladder tumor. Bladder paraganglioma is a rare condition, and understanding possible imaging findings is crucial to raising suspicion of this diagnosis and expanding our knowledge of this rare disease.

Original languageEnglish
Pages (from-to)213-217
Number of pages5
JournalRadiology Case Reports
Volume19
Issue number1
DOIs
StatePublished - Jan 2024

Strategic Focuses

  • Vida Humana Plena (Vita)​

Article Classification

  • Full research article

Indexación Internacional (Artículo)

  • SCOPUS

Scopus-Q Quartil

  • Q4

ISI- Q Quartil

  • Ninguno

Categoría Publindex

  • B

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