2015
DOI: 10.1016/j.otc.2014.12.008
|View full text |Cite
|
Sign up to set email alerts
|

Nonparaganglioma Jugular Foramen Tumors

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

1
16
0

Year Published

2016
2016
2024
2024

Publication Types

Select...
4
2

Relationship

1
5

Authors

Journals

citations
Cited by 23 publications
(17 citation statements)
references
References 62 publications
1
16
0
Order By: Relevance
“…We regard the surgery as crucial treatment for large symptomatic JFMs, although it is challenging for surgical management and radiotherapy became an effective alternative for intracranial meningiomas [6,28,52,61]. Patient selection, including preoperative neuroimaging and neurological assessment, surgical approaches and intraoperative preserving cranial nerves, and postoperative management all correlate with the …”
Section: Surgical Managementmentioning
confidence: 99%
See 1 more Smart Citation
“…We regard the surgery as crucial treatment for large symptomatic JFMs, although it is challenging for surgical management and radiotherapy became an effective alternative for intracranial meningiomas [6,28,52,61]. Patient selection, including preoperative neuroimaging and neurological assessment, surgical approaches and intraoperative preserving cranial nerves, and postoperative management all correlate with the …”
Section: Surgical Managementmentioning
confidence: 99%
“…[21,50,61]. Due to its deepseated complex neurovascular structure, the surgical management of jugular foramen tumors involves multidisciplinary skull base team works and still is a challenge to surgeons [5,36,50,51,61].…”
Section: Introductionmentioning
confidence: 99%
“…Jugular foramen (JF) tumors include jugular paraganglioma (JP), the most common primary tumor of the JF, and less commonly, schwannomas, meningiomas, or metastatic disease. 1,2 Jugular paraganglioma incidence is 1 per 1.3 million people per year; it is more common in women (3-6:1 women:men) and often diagnosed at 40 to 60 years of age. 1-3 Jugular paragangliomas are slow growing and generally considered benign, though local growth may result in symptoms.…”
Section: Introductionmentioning
confidence: 99%
“…1,2 Jugular paraganglioma incidence is 1 per 1.3 million people per year; it is more common in women (3-6:1 women:men) and often diagnosed at 40 to 60 years of age. 1-3 Jugular paragangliomas are slow growing and generally considered benign, though local growth may result in symptoms. All JF lesions are associated with cranial nerve (CN) dysfunction, particularly of the lower CNs, as well as auditory and vestibular symptoms.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation