A Large Malignant Peripheral Nerve Sheath Tumor in the Neurofibromatosis Patient: A Case Report
Journal of the Korean Society of Plastic and Reconstructive Surgeons
; : 761-763, 2006.
Article
en Ko
| WPRIM
| ID: wpr-220370
Biblioteca responsable:
WPRO
ABSTRACT
PURPOSE: Malignant peripheral nerve sheath tumors most often arise from the anatomically discernible peripheral nerve or neurofibroma. METHODS: A 55-year-old man had a rapidly growing pedunculated large mass on the sacrolumbar junction for 2 years. He has congenital neurofibromatosis type I. He had multiple caf-au-lait spots and multiple neurofibromas on the entire body. The mass developed from a subcutaneous nodule on the sacrolumbar junction and grew rapidly. The preoperative punch biopsy revealed a malignant peripheral nerve tumor. The mass was completely excised with 1 cm free margin above the deep fascial plane. RESULTS: There was no evidence of recurrence of tumor for 19 months of follow-up examination. CONCLUSION: Malignant peripheral nerve sheath tumor is very rare and has unique feature. We report a successful case of malignant peripheral nerve sheath tumor with the review of the literatures.
Palabras clave
Texto completo:
1
Índice:
WPRIM
Asunto principal:
Neoplasias del Sistema Nervioso Periférico
/
Nervios Periféricos
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Recurrencia
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Biopsia
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Estudios de Seguimiento
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Neurofibromatosis 1
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Neurofibromatosis
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Neurilemoma
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Neurofibroma
Tipo de estudio:
Observational_studies
/
Prognostic_studies
Límite:
Humans
Idioma:
Ko
Revista:
Journal of the Korean Society of Plastic and Reconstructive Surgeons
Año:
2006
Tipo del documento:
Article