2018
DOI: 10.1016/j.purol.2018.06.003
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Retro-peritoneal paraganglioma, diagnosis and management

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Cited by 5 publications
(3 citation statements)
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“…The remaining 15-20% of pheochromocytomas are extra-adrenal (termed paragangliomas) and usually located close to the sympathetic chain, such as in the head and neck, thoracic cavity, and retroperitoneal cavity [19][20][21]. Extra-adrenal retroperitoneal paragangliomas without prominent clinical manifestations (e.g., headache, perspiration, and palpitations) resulting from the release of catecholamine are commonly misdiagnosed as other retroperitoneal masses [22][23][24]. Compared with adrenal pheochromocytoma, extra-adrenal retroperitoneal paraganglioma has some significant characteristics, such as high misdiagnosis rate and complicated anatomic structure [25,26].…”
Section: Discussion/conclusionmentioning
confidence: 99%
“…The remaining 15-20% of pheochromocytomas are extra-adrenal (termed paragangliomas) and usually located close to the sympathetic chain, such as in the head and neck, thoracic cavity, and retroperitoneal cavity [19][20][21]. Extra-adrenal retroperitoneal paragangliomas without prominent clinical manifestations (e.g., headache, perspiration, and palpitations) resulting from the release of catecholamine are commonly misdiagnosed as other retroperitoneal masses [22][23][24]. Compared with adrenal pheochromocytoma, extra-adrenal retroperitoneal paraganglioma has some significant characteristics, such as high misdiagnosis rate and complicated anatomic structure [25,26].…”
Section: Discussion/conclusionmentioning
confidence: 99%
“…Paraganglioma (PGL), also known as extra-adrenal pheochromocytoma, is a rare tumor that develops in the paraganglia, specialized cells along the sympathetic or parasympathetic nervous system[ 1 ]. These tumors can be found in various locations such as the carotid body, aortic body, and other parasympathetic ganglia[ 2 ].…”
Section: Introductionmentioning
confidence: 99%
“…The World Health Organization decided to assign the term “pheochromocytoma” to refer exclusively to tumors occurring in the adrenal medulla and “extra-adrenal PGLs” as tumors occurring in other tissues [ 1 ]. PGL is a rare neuroendocrine neoplasm observed in patients of all ages, with an estimated incidence of 3/1,000,000 [ 2 ]. Abdominal PGLs can be located in the organ of Zuckerkandl, which lies anteriorly to the aortic bifurcation, but they can also be found in paraaortic locations, in the bladder base, or even in the pancreas, liver, and mesentery [ 3 ].…”
Section: Introductionmentioning
confidence: 99%