Adrenal ganglioneuroma: What you need to know.

Published

Journal Article (Review)

Adrenal ganglioneuromas (GNs) constitute rare, differentiated tumors which originate from neural crest cells. GNs are usually hormonally silent and tend to be discovered incidentally on imaging tests. Adrenalectomy is the gold standard for the treatment of primary adrenal GNs. Nevertheless, preoperative differential diagnosis of GNs remains extremely challenging, and thus histopathological examination is required in order to confirm the diagnosis of GN. Overall, prognosis after surgical resection seems to be excellent, without any recurrences or need for adjuvant therapy.

Full Text

Duke Authors

Cited Authors

  • Mylonas, KS; Schizas, D; Economopoulos, KP

Published Date

  • October 2017

Published In

Volume / Issue

  • 5 / 10

Start / End Page

  • 373 - 377

PubMed ID

  • 29085827

Pubmed Central ID

  • 29085827

Electronic International Standard Serial Number (EISSN)

  • 2307-8960

International Standard Serial Number (ISSN)

  • 2307-8960

Digital Object Identifier (DOI)

  • 10.12998/wjcc.v5.i10.373

Language

  • eng