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A Large Malignant Peripheral Nerve Sheath Tumor in the Neurofibromatosis Patient: A Case Report
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.
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Texto completo: 1 Índice: WPRIM Asunto principal: Neoplasias del Sistema Nervioso Periférico / Nervios Periféricos / Recurrencia / Biopsia / Estudios de Seguimiento / Neurofibromatosis 1 / Neurofibromatosis / Neurilemoma / 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
Texto completo: 1 Índice: WPRIM Asunto principal: Neoplasias del Sistema Nervioso Periférico / Nervios Periféricos / Recurrencia / Biopsia / Estudios de Seguimiento / Neurofibromatosis 1 / Neurofibromatosis / Neurilemoma / 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