Solitary paraganglioma of the hypoglossal nerve: case report.

Hdl Handle:
http://hdl.handle.net/10147/141001
Title:
Solitary paraganglioma of the hypoglossal nerve: case report.
Authors:
Raza, Kazim; Kaliaperumal, Chandrasekaran; Farrell, Michael; O'Dwyer, John A; Pidgeon, Christopher
Affiliation:
Department of Neurosurgery, National Centre for Neurosurgery, Beaumont Hospital, Dublin, Republic of Ireland.
Citation:
Solitary paraganglioma of the hypoglossal nerve: case report. 2011, 68 (4):E1170-4; discussion E1174 Neurosurgery
Journal:
Neurosurgery
Issue Date:
Apr-2011
URI:
http://hdl.handle.net/10147/141001
DOI:
DOI: 10.1227/NEU.0b013e31820a16b5
PubMed ID:
21792092
Additional Links:
http://www.ncbi.nlm.nih.gov/pubmed/21792092
Abstract:
BACKGROUND AND IMPORTANCE: We report the case history of solitary hypoglossal paraganglioma in a 64-year-old woman. The surgical difficulties encountered in the removal of this challenging tumor are discussed and as a literature review provided. CLINICAL PRESENTATION: A 64-year-old woman presented with a short history of dysphonia, occasional dysphagia, tinnitus, altered taste, and unilateral left-sided tongue wasting. On examination, there was left lower motor hypoglossal paralysis. Imaging showed a discrete enhancing lobulated mass, measuring 2 × 2 cm, in the region of the hypoglossal nerve extending into the hypoglossal canal suggestive of hypoglossal paraganglioma. A left dorsolateral suboccipital craniotomy was performed with the patient in the sitting position. The hypoglossal nerve appeared to be enlarged, and the jugular foramen was normal. Complete surgical debulking of the tumor was not attempted because of its vascular nature. The nerve was decompressed, and neuropathology confirmed a low-grade paraganglioma arising from the hypoglossal nerve. The patient was scheduled to receive stereotactic radiation for further management. CONCLUSION: When a case of solitary hypoglossal paraganglioma is encountered in clinical practice, the aim of management should be mainly focused on achieving a diagnosis and preserving the hypoglossal nerve function. If there is evidence of vascularity in the lesion noted on magnetic resonance imaging, a preoperative angiogram should be obtained with a view for embolization. We decompressed the hypoglossal canal and achieved good improvement in the patient's symptoms. We recommend stereotactic radiosurgery for remnant and small hypoglossal tumors and regular follow-up with magnetic resonance imaging scans.
Item Type:
Article
Language:
en
ISSN:
1524-4040

Full metadata record

DC FieldValue Language
dc.contributor.authorRaza, Kazimen
dc.contributor.authorKaliaperumal, Chandrasekaranen
dc.contributor.authorFarrell, Michaelen
dc.contributor.authorO'Dwyer, John Aen
dc.contributor.authorPidgeon, Christopheren
dc.date.accessioned2011-08-29T09:19:46Z-
dc.date.available2011-08-29T09:19:46Z-
dc.date.issued2011-04-
dc.identifier.citationSolitary paraganglioma of the hypoglossal nerve: case report. 2011, 68 (4):E1170-4; discussion E1174 Neurosurgeryen
dc.identifier.issn1524-4040-
dc.identifier.pmid21792092-
dc.identifier.doiDOI: 10.1227/NEU.0b013e31820a16b5-
dc.identifier.urihttp://hdl.handle.net/10147/141001-
dc.description.abstractBACKGROUND AND IMPORTANCE: We report the case history of solitary hypoglossal paraganglioma in a 64-year-old woman. The surgical difficulties encountered in the removal of this challenging tumor are discussed and as a literature review provided. CLINICAL PRESENTATION: A 64-year-old woman presented with a short history of dysphonia, occasional dysphagia, tinnitus, altered taste, and unilateral left-sided tongue wasting. On examination, there was left lower motor hypoglossal paralysis. Imaging showed a discrete enhancing lobulated mass, measuring 2 × 2 cm, in the region of the hypoglossal nerve extending into the hypoglossal canal suggestive of hypoglossal paraganglioma. A left dorsolateral suboccipital craniotomy was performed with the patient in the sitting position. The hypoglossal nerve appeared to be enlarged, and the jugular foramen was normal. Complete surgical debulking of the tumor was not attempted because of its vascular nature. The nerve was decompressed, and neuropathology confirmed a low-grade paraganglioma arising from the hypoglossal nerve. The patient was scheduled to receive stereotactic radiation for further management. CONCLUSION: When a case of solitary hypoglossal paraganglioma is encountered in clinical practice, the aim of management should be mainly focused on achieving a diagnosis and preserving the hypoglossal nerve function. If there is evidence of vascularity in the lesion noted on magnetic resonance imaging, a preoperative angiogram should be obtained with a view for embolization. We decompressed the hypoglossal canal and achieved good improvement in the patient's symptoms. We recommend stereotactic radiosurgery for remnant and small hypoglossal tumors and regular follow-up with magnetic resonance imaging scans.-
dc.language.isoenen
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pubmed/21792092en
dc.titleSolitary paraganglioma of the hypoglossal nerve: case report.en
dc.typeArticleen
dc.contributor.departmentDepartment of Neurosurgery, National Centre for Neurosurgery, Beaumont Hospital, Dublin, Republic of Ireland.en
dc.identifier.journalNeurosurgeryen
dc.description.provinceLeinster-

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