Imperatore Vittorio, Creta Massimiliano, Di Meo Sergio, Buonopane Roberto, Spirito Lorenzo, Fusco Ferdinando, Longo Nicola, Forte Nicola Rosario, Mirone Vincenzo
Operative Unit of Urology, Buon Consiglio Hospital - Fatebenefratelli, Naples.
Arch Ital Urol Androl. 2017 Dec 31;89(4):319-320. doi: 10.4081/aiua.2017.4.319.
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.
副神经节瘤(PGL)是起源于副神经节的自主神经系统罕见神经内分泌肿瘤。尽管PGL可发生于存在生理性副神经节组织的任何部位,但在小骨盆中的定位极为罕见。PGL可能具有激素活性并将多余的儿茶酚胺释放到血液中,也可能无活性。无症状病例带来诊断难题。我们描述了一例发生在小骨盆侧壁的无症状PGL病例,该病例表现为一名男性患者偶然发现的无症状肿块。