Malignant pelvic paraganglioma: A case report.
Malignant
Paraganglioma
Pelvis
Journal
Radiology case reports
ISSN: 1930-0433
Titre abrégé: Radiol Case Rep
Pays: Netherlands
ID NLM: 101467888
Informations de publication
Date de publication:
Jul 2022
Jul 2022
Historique:
received:
19
12
2021
revised:
27
03
2022
accepted:
30
03
2022
entrez:
16
5
2022
pubmed:
17
5
2022
medline:
17
5
2022
Statut:
epublish
Résumé
Pheochromocytomas arising from outside the adrenal glands are called paragangliomas and constitute a rare disease and can occur in the pelvic retroperitoneum. Symptoms of excess catecholamine production, as well as elevated urine vanillylmandelic acid levels and serum and urine norepinephrine levels, are highly diagnostic for paraganglioma. Imaging can be helpful for the diagnostic of these pelvic tumors, differentiating them from other pelvic masses. We hereby present a case of pelvic malignant paraganglioma.
Identifiants
pubmed: 35570870
doi: 10.1016/j.radcr.2022.03.112
pii: S1930-0433(22)00285-0
pmc: PMC9096467
doi:
Types de publication
Case Reports
Langues
eng
Pagination
2342-2345Informations de copyright
© 2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington.
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