Publication:
Retrospective study on extracranial neck schwannomas in tertiary care hospital in Nepal

creativeworkseries.issnISSN (Print) : 1993-2979 | ISSN (Online) : 1993-2987
dc.contributor.authorShrestha, UK
dc.contributor.authorShrestha, KR
dc.date.accessioned2026-05-07T09:01:06Z
dc.date.available2026-05-07T09:01:06Z
dc.date.issued2014
dc.descriptionUK Shrestha Department of Cardiothoracic and Vascular Surgery, Manmohan Cardiothoracic Vascular and Transplant Center, Kathmandu, Nepal KR Shrestha Department of Cardiothoracic and Vascular Surgery, Manmohan Cardiothoracic Vascular and Transplant Center, Kathmandu, Nepal
dc.description.abstractAbstract Introduction: Schwannomas are relatively rare tumors arising from Schwann cells that ensheath the peripheral nerves. The study aim was to identify extracranial neck schwannomas treated in a tertiary care hospital in Nepal. Methods: We reviewed medical records of all patients with extracranial head and neck schwannomas treated at our department from July 2004 to June 2014. Results: Ten such patients consisted of 7 males and 3 females were identified, with a mean age of 37.8 +/- 10.7 years (range: 20 to 54 years) with solitary schwannomas. Mean size of tumor was 5 cm (range: 2-10 cm). Most of the patients (60%) presented with asymptomatic palpable mass. Of these ten, 50% had a left sided neck mass. Seven originated from vagus nerve while three from sympathetic chain. The average duration of symptoms ranged from one month to two and half years. In all cases, tumor was completely resected through cervical approach. All tumors were enucleated keeping nerve of origin intact. In all cases, the tumor was completely resected surgically. The average follow up period ranged from one month to 108 months (median: 24 months). No major postoperative complications were noted. Two patients (20%) developed Homer's syndrome and one (10%) had temporary hypoglossal nerve palsy which recovered within three months. Conclusion: Non-vestibular extracranial head and neck schwannomas most frequently present as an innocuous longstanding unilateral neck mass. The mainstay of treatment is complete excision preserving the nerve of origin. Early recognition of Schwannomas is key to optimal treatment. Keywords: cranial nerves, Horner's syndrome, Schwannoma
dc.identifierhttps://doi.org/10.59779/jiomnepal.647
dc.identifier.urihttps://hdl.handle.net/20.500.14572/6054
dc.language.isoen_US
dc.publisherInstitute of Medicine
dc.subjectcranial nerves
dc.subjectHorner's syndrome
dc.subjectSchwannoma
dc.titleRetrospective study on extracranial neck schwannomas in tertiary care hospital in Nepal
dc.typeArticle
dspace.entity.typePublication
local.article.typeOriginal Article
oaire.citation.endPage91
oaire.citation.startPage87
relation.isJournalIssueOfPublicationc837dc47-976e-4e95-ba7a-91ce7e563aaf
relation.isJournalIssueOfPublication.latestForDiscoveryc837dc47-976e-4e95-ba7a-91ce7e563aaf
relation.isJournalOfPublicationa9ba45d9-ee33-4a6b-b1fc-6626b87eec6c

Files

Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
87-91.pdf
Size:
777.02 KB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.86 KB
Format:
Item-specific license agreed to upon submission
Description:

Collections