Bladder Paraganglioma With Rapid Metastasis: A Case Report and Review of the Literature

Read full text
Authors: James P. Turney, Gabrielle R. Yankelevich, Matvey Tsivian
Cited by: 0
References: 14

Abstract

Bladder paragangliomas (bPGLs) are extremely rare tumors, and we present a unique case of metastatic bPGL that developed within three months. Frequently, these tumors are related to a hereditary syndrome due to germline mutations in succinate dehydrogenase B (SDHB). A unique challenge in this case was related to social determinants of health, which, in this patient, were associated with difficulty maintaining appointments. In treating a patient with hematuria, it is important to consider paraganglioma (PGL) as a differential diagnosis to optimize treatment.

Fields of Study & Subjects

Adrenal and Paraganglionic Tumors Hormonal Regulation and Hypertension Cancer Hypoxia and Metabolism

Publication details

Journal / source
Cureus
Volume
18
Issue
1
Pages
e100705–e100705
Publication date
3 January 2026
Language
EN