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Incidentally discovered pelvic paraganglioma: A case report

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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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Imad Ghantous, Aziz Najjar, Yehya Tlaiss, Samer Danaf, Camil J Chouairy (2023)
Resection of Retroperitoneal Extra-Adrenal Pheochromocytoma: A Case Report. Cureus,
10.7759/cureus.43185

How to Cite

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