Incidentally discovered pelvic paraganglioma: A case report

Submitted: August 1, 2017
Accepted: September 16, 2017
Published: December 31, 2017
Abstract Views: 1033
PDF: 585
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Paragangliomas (PGL) are rare neuroendocrine tumors of the autonomic nervous system originating from paraganglia. Although PGL may arise at any site where physiologic paraganglionic tissue exists, the localization in the small pelvis is extremely rare. PGL may be hormonally active and release surplus catecholamines into the blood or inactive. The asymptomatic cases pose a diagnostic dilemma. We describe the case of an asymptomatic PGL arising in the small pelvis sidewall presenting as an incidentally discovered asymptomatic mass in a male subject.

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Imperatore, V., Creta, M., Di Meo, S., Buonopane, R., Spirito, L., Fusco, F., Longo, N., Forte, N. R., & Mirone, V. (2017). Incidentally discovered pelvic paraganglioma: A case report. Archivio Italiano Di Urologia E Andrologia, 89(4), 319–320. https://doi.org/10.4081/aiua.2017.4.319