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PubMed · 10785927

[Bladder pheochromocytoma].

F Attyaoui·Y Nouira·I Kbaier·A Ben Younes·A Horchani
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Abstract

OBJECTIVE: Report of a new case of a rare bladder tumour: bladder phaeochromocytoma. MATERIAL AND METHODS: A 45-year-old patient presented with paroxysmal symptoms consisting of headaches, palpitations, tinnitus and excessive sweating after each micturition. Complementary investigations: ultrasonography, intravenous urography and magnetic resonance imaging, suggested a circumscribed tumour with a 2 cm long axis in the bladder dome, and the diagnosis of bladder phaeochromocytoma was proposed. Partial cystectomy was performed. RESULTS: The postoperative course was uneventful and the subsequent outcome was favourable with resolution of all symptoms with a follow-up of 28 months. Histological examination of the operative specimen confirmed the diagnosis of bladder phaeochromocytoma. CONCLUSION: Bladder phaeochromocytoma is a rare tumour. Treatment of this lesion requires the same preparation as for any other site of phaeochromocytoma. Partial cystectomy ensures radical and effective treatment. Long-term surveillance is necessary, as recurrences or metastases have been described 20 and 40 years after treatment.

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FemaleHumansMiddle AgedPheochromocytomaUrinary Bladder NeoplasmsCase ReportsEnglish AbstractJournal Article

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F Attyaoui, Y Nouira, I Kbaier, A Ben Younes, A Horchani. 2000. [Bladder pheochromocytoma].. https://pubmed.ncbi.nlm.nih.gov/10785927/

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