지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2013.1
- 수록면
- 57 - 61 (5page)
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초록· 키워드
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Background Von Recklinghausen disease or neurofibromatosis type 1 is an autosomal dominant genetic disorder of chromosome 17q11.2. The most common characteristic findings of NF 1 include multiple and recurrent cutaneous neurofibromas associated with psychosocial distress. Methods Sixteen patients (9 female, 7 male; average age, 31 years; range, 16 to 67 years) with multiple cutaneous neurofibromas between March 2010 and February 2012 were included in the study. All patients were treated with radiosurgical ablation and excision under general anesthesia. Results All 16 patients were satisfied with the results, when questioned directly during the outpatient department follow-up. The only complaint from a few patients was minimal scarring, but acceptable results were obtained in the end. Conclusions The radiofrequency procedure is almost bloodless and quick, creating a smaller necrotizing zone. Therefore, instead of employing the time consuming traditional surgery, such as laser therapy and electrosurgical excision, that produces uncertain results and can affect normal adjacent tissue, treatment of neurofibromas with radiofrequency ablation and excision can be an alternative choice of treatment for patients with a large number of neurofibromas.
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등록된 정보가 없습니다.
참고문헌 (13)
참고문헌 신청
Huson SM / 2008 / The neurofibromatoses: classification, clinical features and genetic counseling / Karger :1~20
Needle MN / 1997 / Prognostic signs in the surgical management of plexiform neurofibroma: the Children’s Hospital of Philadelphia experience, 1974-1994 / J Pediatr 131:678~682
Riccardi VM / 1992 / Neurofibromatosis: phenotype, natural history, and pathogenesis / Johns Hopkins University Press
Huson SM / 1988 / Von Recklinghausen neurofibromatosis. A clinical and population study in south-east Wales / Brain 111:1355~1381
Listernick R / 1997 / Optic pathway gliomas in children with neurofibromatosis 1: consensus statement from the NF1 Optic Pathway Glioma Task Force / Ann Neurol 41:143~149
Needle MN / 1997 / Prognostic signs in the surgical management of plexiform neurofibroma: the Children’s Hospital of Philadelphia experience, 1974-1994 / J Pediatr 131:678~682
Riccardi VM / 1992 / Neurofibromatosis: phenotype, natural history, and pathogenesis / Johns Hopkins University Press
Huson SM / 1988 / Von Recklinghausen neurofibromatosis. A clinical and population study in south-east Wales / Brain 111:1355~1381
Listernick R / 1997 / Optic pathway gliomas in children with neurofibromatosis 1: consensus statement from the NF1 Optic Pathway Glioma Task Force / Ann Neurol 41:143~149
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