Spinal Ganglioneuroma.


Journal

World neurosurgery
ISSN: 1878-8769
Titre abrégé: World Neurosurg
Pays: United States
ID NLM: 101528275

Informations de publication

Date de publication:
06 2022
Historique:
received: 21 01 2022
revised: 10 03 2022
accepted: 11 03 2022
pubmed: 21 3 2022
medline: 9 6 2022
entrez: 20 3 2022
Statut: ppublish

Résumé

An otherwise healthy 57-year-old man presented with intermittent low back pain and was incidentally found to have a left-sided paraspinal mass invading the spinal canal and causing spinal cord compression. He underwent a T11-12 hemilaminectomy, facetectomy, and instrumented fusion for a gross total resection with a good clinical outcome. Pathology revealed the lesion to be a ganglioneuroma. Ganglioneuroma is a rare and interesting pathology. These tumors are benign peripheral neuroblastic tumors derived from the neural crest and found along the entire neuroaxis. Tumors come to clinical attention if they cause symptomatic compression of neural structures or are found incidentally on imaging. Additionally, as these tumors share a common lineage with pheochromocytomas, systemic symptoms can be observed resulting from secretion of vasoactive peptides. The pathologic diagnosis of ganglioneuroma is predominantly based on morphology.

Identifiants

pubmed: 35306201
pii: S1878-8750(22)00337-0
doi: 10.1016/j.wneu.2022.03.046
pii:
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

15-16

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Auteurs

Jacob L Goldberg (JL)

Department of Neurosurgery, New York Presbyterian Hospital, New York, New York. Electronic address: jag9177@nyp.org.

Jiankun Tong (J)

Department of Pathology, New York Presbyterian Hospital, New York, New York.

Lynn B McGrath (LB)

Department of Neurosurgery, New York Presbyterian Hospital, New York, New York.

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Classifications MeSH