ArticleBladder (San Francisco, Calif.)2025
Incidental paraganglioma of the urinary bladder: A case series highlighting a rare entity and a urologist's nightmare.
Article in Bladder (San Francisco, Calif.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
2 citing papers in PubMed.
- Article
- Case report and literature review: key clinical management points and prognostic analysis of paraganglioma of the urinary bladder.Frontiers in surgery · 2026Article
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5 authors.
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No grant is acknowledged in the PubMed record.
Abstract
Background: Pheochromocytomas originate from chromaffin cells of the adrenal medulla, resulting in excessive production of catecholamines and bizarre clinical symptoms. An extra-adrenal pheochromocytoma is called a paraganglioma. Urinary bladder paraganglioma represents an uncommon tumor that accounts for <0.05% of all bladder tumors. Case presentation: Presented here are three cases of incidental urinary bladder paraganglioma, all having hematuria as the primary symptom. During transurethral resection of bladder tumor, blood pressure fluctuated intensely with profuse bleeding, leading to the abandonment of the procedure. The patients were later diagnosed as having paraganglioma, and then, they were subjected to systemic evaluation and definitive treatment. Conclusion: Although bladder paraganglioma is a rare condition, it should be strongly suspected if a patient who has no definitive symptoms of the disease developed a sudden hemodynamic change at the very start of the procedure.
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