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. 2013 Apr 29:13:22.
doi: 10.1186/1471-2490-13-22.

Pheochromocytoma of the urinary bladder: a systematic review of the contemporary literature

Pheochromocytoma of the urinary bladder: a systematic review of the contemporary literature

Jonathan A Beilan et al. BMC Urol. .

Abstract

Background: Pheochromocytoma (paraganglioma) of the urinary bladder is a rare tumor. Herein we sought to review the contemporary literature on pheochromocytomas of the urinary bladder in order to further illustrate the presentation, treatment options and outcomes of patients diagnosed with these tumors.

Methods: A comprehensive review of the current literature was conducted according to the PRISMA guidelines by accessing the NCBI PubMed database and using the search terms "paraganglioma, pheochromocytoma, bladder." This search resulted in the identification of 186 articles published between January 1980 and April 2012 of which 80 articles were ultimately included in our analysis.

Results: Pheochromocytomas usually occurred in young adult Caucasians (mean age, 43.3 years; range,11-84 years). According to the literature, the most common symptoms and signs of pheochromocytomas of the urinary bladder were hypertension, headache, and hematuria. Of the 77 cases that commented on catecholamine production, 65 patients had biochemically functional tumors. Approximately 20% of patients were treated by transurethral resection alone, 70% by partial cystectomy and 10% by radical cystectomy. The 75 patients with follow-up information had a mean follow-up of 35 months. At the time of last follow-up, 15 (14.2%) had disease recurrence, 10 (9.4%) had metastasis, and 65 (61.3%) were alive.

Conclusions: Pheochromocytomas of the urinary bladder tend to be functional and occur mostly in young adult Caucasians. Patients with localized tumors have an extremely favorable prognosis and may be managed by less aggressive modalities, whereas patients with metastatic disease have a significant reduction in survival rates despite aggressive treatment.

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Figure 1
Literature search schema.

References

    1. Sheps SG, Jiang NS, Klee GG. Recent developments in the diagnosis and treatment of pheochromocytoma. Mayo Clin Proc. 1990;65:88–95. doi: 10.1016/S0025-6196(12)62113-2. - DOI - PubMed
    1. Zhou M, Epstein JI, Young RH. Paraganglioma of the urinary bladder: a lesion that may be misdiagnosed as urothelial carcinoma in transurethral resection specimens. Am J Surg Pathol. 2004;28:94–100. doi: 10.1097/00000478-200401000-00011. - DOI - PubMed
    1. Zimmerman IJ, Biron RE, Macmahon HE. Pheochromocytoma of the urinary bladder. N Engl J Med. 1953;249:25–26. doi: 10.1056/NEJM195307022490106. - DOI - PubMed
    1. Moher D, Liberati A, Tetzlaff J, Altman DG. PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med. 2009;6(7):e1000097. doi: 10.1371/journal.pmed.1000097. - DOI - PMC - PubMed
    1. Tsai CC, Wu WJ, Chueh KS, Li WM, Huang CH, Wu CC, Lee MH, Chen SM. Paraganglioma of the urinary bladder first presented by bladder bloody tamponade: two case reports and review of the literatures. Kaohsiung J Med Sci. 2011;27(3):108–113. doi: 10.1016/j.kjms.2010.05.005. - DOI - PMC - PubMed

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