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Clinical Presentation and Management of Jugular Foramen Paraganglioma

OBJECTIVES: Jugular foramen paraganglioma is a locally invasive, benign tumor, which grow slowly and causes various symptoms such as pulsatile tinnitus and low cranial nerve palsy. Complete surgical resection is regarded as the ideal management of these tumors. The goal of this study is to identify...

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Autores principales: Chung, Sa Myung, Kim, Hyun Su, Jung, Jinsei, Lee, Ho-Ki, Lee, Won Sang
Formato: Texto
Lenguaje:English
Publicado: Korean Society of Otorhinolaryngology-Head and Neck Surgery 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2671826/
https://www.ncbi.nlm.nih.gov/pubmed/19434288
http://dx.doi.org/10.3342/ceo.2009.2.1.28
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author Chung, Sa Myung
Kim, Hyun Su
Jung, Jinsei
Lee, Ho-Ki
Lee, Won Sang
author_facet Chung, Sa Myung
Kim, Hyun Su
Jung, Jinsei
Lee, Ho-Ki
Lee, Won Sang
author_sort Chung, Sa Myung
collection PubMed
description OBJECTIVES: Jugular foramen paraganglioma is a locally invasive, benign tumor, which grow slowly and causes various symptoms such as pulsatile tinnitus and low cranial nerve palsy. Complete surgical resection is regarded as the ideal management of these tumors. The goal of this study is to identify the clinical characteristics and most effective surgical approach for jugular foramen paraganglioma. METHODS: Retrospective analysis of 9 jugular foramen paraganglioma patients who underwent surgical resection between 1986 and 2005 was performed. Clinical records were reviewed for analysis of initial clinical symptoms and signs, audiological examinations, neurological deficits, radiological features, surgical approaches, extent of resection, treatment outcomes and complications. RESULTS: Most common initial symptom was hoarseness, followed by pulsatile tinnitus. Seven out of 9 patients had at least one low cranial nerve palsy. Seven patients were classified as Fisch Type C tumor and remaining 2 as Fisch Type D tumor on radiologic examination. Total of 11 operations took place in 9 patients. Total resection was achieved in 6 cases, when partial resection was done in 3 cases. Two patients with partial resection received gamma knife radiosurgery (GKS), when remaining 1 case received both GKS and two times of revision operation. No mortality was encountered and there were few postoperative complications. CONCLUSION: Neurologic examination of low cranial nerve palsy is crucial since most patients had at least one low cranial nerve palsy. All tumors were detected in advanced stage due to slow growing nature and lack of symptom. Angiography with embolization is crucial for successful tumor removal without massive bleeding. Infratemporal fossa approach can be considered as a safe, satisfactory approach for removal of jugular foramen paragangliomas. In tumors with intracranial extension, combined approach is recommended in that it provides better surgical view and can maintain the compliance of the patients.
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spelling pubmed-26718262009-05-11 Clinical Presentation and Management of Jugular Foramen Paraganglioma Chung, Sa Myung Kim, Hyun Su Jung, Jinsei Lee, Ho-Ki Lee, Won Sang Clin Exp Otorhinolaryngol Original Article OBJECTIVES: Jugular foramen paraganglioma is a locally invasive, benign tumor, which grow slowly and causes various symptoms such as pulsatile tinnitus and low cranial nerve palsy. Complete surgical resection is regarded as the ideal management of these tumors. The goal of this study is to identify the clinical characteristics and most effective surgical approach for jugular foramen paraganglioma. METHODS: Retrospective analysis of 9 jugular foramen paraganglioma patients who underwent surgical resection between 1986 and 2005 was performed. Clinical records were reviewed for analysis of initial clinical symptoms and signs, audiological examinations, neurological deficits, radiological features, surgical approaches, extent of resection, treatment outcomes and complications. RESULTS: Most common initial symptom was hoarseness, followed by pulsatile tinnitus. Seven out of 9 patients had at least one low cranial nerve palsy. Seven patients were classified as Fisch Type C tumor and remaining 2 as Fisch Type D tumor on radiologic examination. Total of 11 operations took place in 9 patients. Total resection was achieved in 6 cases, when partial resection was done in 3 cases. Two patients with partial resection received gamma knife radiosurgery (GKS), when remaining 1 case received both GKS and two times of revision operation. No mortality was encountered and there were few postoperative complications. CONCLUSION: Neurologic examination of low cranial nerve palsy is crucial since most patients had at least one low cranial nerve palsy. All tumors were detected in advanced stage due to slow growing nature and lack of symptom. Angiography with embolization is crucial for successful tumor removal without massive bleeding. Infratemporal fossa approach can be considered as a safe, satisfactory approach for removal of jugular foramen paragangliomas. In tumors with intracranial extension, combined approach is recommended in that it provides better surgical view and can maintain the compliance of the patients. Korean Society of Otorhinolaryngology-Head and Neck Surgery 2009-03 2009-03-26 /pmc/articles/PMC2671826/ /pubmed/19434288 http://dx.doi.org/10.3342/ceo.2009.2.1.28 Text en Copyright © 2009 Korean Society of Otorhinolaryngology-Head and Neck Surgery http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Chung, Sa Myung
Kim, Hyun Su
Jung, Jinsei
Lee, Ho-Ki
Lee, Won Sang
Clinical Presentation and Management of Jugular Foramen Paraganglioma
title Clinical Presentation and Management of Jugular Foramen Paraganglioma
title_full Clinical Presentation and Management of Jugular Foramen Paraganglioma
title_fullStr Clinical Presentation and Management of Jugular Foramen Paraganglioma
title_full_unstemmed Clinical Presentation and Management of Jugular Foramen Paraganglioma
title_short Clinical Presentation and Management of Jugular Foramen Paraganglioma
title_sort clinical presentation and management of jugular foramen paraganglioma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2671826/
https://www.ncbi.nlm.nih.gov/pubmed/19434288
http://dx.doi.org/10.3342/ceo.2009.2.1.28
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