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      KCI등재후보 SCOPUS SCIE

      Clinical Presentation and Management of Jugular Foramen Paraganglioma

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      https://www.riss.kr/link?id=A101596835

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      다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

      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.
      번역하기

      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 the...

      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.

      더보기

      다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

      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.
      번역하기

      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 t...

      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.

      더보기

      참고문헌 (Reference)

      1 Heth J, "The basic science of glomus jugulare tumors" 17 (17): E2-, 2004

      2 Woods CI, "Surgery for glomus tumors: the Otology Group experience" 103 (103): 65-70, 1993

      3 Mascarenhas F, "Stereostatic radiosurgery in the management of glomus jugulare tumors. in: Radiosurgery" Karger 108-117, 2006

      4 Valavanis A, "Preoperative embolization of the head and neck: indications, patient selection, goals, and precautions" 7 (7): 943-952, 1986

      5 Ramina R, "Jugular foramen tumors: diagnosis and treatment" 17 (17): E5-, 2004

      6 Watkins LD, "Glomus jugulare tumours: a review of 61 cases" 130 (130): 66-70, 1994

      7 Michael LM 2nd, "Glomus jugulare tumors: historical overview of the management of this disease" 17 (17): E1-, 2004

      8 Jackson CG, "Glomus jugulare tumors with intracranial ex" 17 (17): E7-, 2004

      9 Coles MC, "Glomus jugulare tumor presentation and management: a case study" 36 (36): 221-223, 2004

      10 Jackson CG, "Defect reconstruction and cerebrospinal fluid management in neurotologic skull base tumors with intracranial extension" 102 (102): 1205-1214, 1992

      1 Heth J, "The basic science of glomus jugulare tumors" 17 (17): E2-, 2004

      2 Woods CI, "Surgery for glomus tumors: the Otology Group experience" 103 (103): 65-70, 1993

      3 Mascarenhas F, "Stereostatic radiosurgery in the management of glomus jugulare tumors. in: Radiosurgery" Karger 108-117, 2006

      4 Valavanis A, "Preoperative embolization of the head and neck: indications, patient selection, goals, and precautions" 7 (7): 943-952, 1986

      5 Ramina R, "Jugular foramen tumors: diagnosis and treatment" 17 (17): E5-, 2004

      6 Watkins LD, "Glomus jugulare tumours: a review of 61 cases" 130 (130): 66-70, 1994

      7 Michael LM 2nd, "Glomus jugulare tumors: historical overview of the management of this disease" 17 (17): E1-, 2004

      8 Jackson CG, "Glomus jugulare tumors with intracranial ex" 17 (17): E7-, 2004

      9 Coles MC, "Glomus jugulare tumor presentation and management: a case study" 36 (36): 221-223, 2004

      10 Jackson CG, "Defect reconstruction and cerebrospinal fluid management in neurotologic skull base tumors with intracranial extension" 102 (102): 1205-1214, 1992

      11 Al-Mefty O, "Complex tumors of the glomus jugulare: criteria, treatment, and outcome" 97 (97): 1356-1366, 2002

      12 Prabhu SS, "Complete resection of a complex glomus jugulare tumor with extensive venous involvement: case report" 17 (17): E12-, 2004

      13 Patel SJ, "Combined approaches for resection of extensive glomus jugulare tumors. A review of 12 cases" 80 (80): 1026-1038, 1994

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      학술지등록 한글명 : Clinical and Experimental Otorhinolaryngology
      외국어명 : Clinical and Experimental Otorhinolaryngology
      2023 평가 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 등재 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2013-10-01 등재 등재학술지 선정 (기타) KCI등재
      2012-01-01 등재 등재후보학술지 유지 (기타) KCI등재후보
      2011-01-01 등재 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2009-01-01 등재 등재후보학술지 선정 (신규평가) KCI등재후보
      2007-06-14 학회명변경 영문명 : Korean Society Of Otolaryngology -> Korean Society of Otorhinolaryngology-Head and Neck Surgery
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.14 0.1 0.84
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.71 0.6 0.324 0
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