Cargando…

Soft tissue sarcoma in neurofibromatosis type 1: A rare case of malignant peripheral nerve sheath tumor of the skin

Malignant peripheral nerve sheath tumor (MPNST) is a rare and often aggressive soft tissue sarcoma originating from the sheaths of peripheral nerves. Approximately 50% of MPNSTs occur in patients with neurofibromatosis (NF). These tumors often present as deep soft tissue lesions, arising from the ne...

Descripción completa

Detalles Bibliográficos
Autores principales: Chung, Young Hun, Jang, Jin Woo, Cho, Jae Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Plastic and Reconstructive Surgeons 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6976743/
https://www.ncbi.nlm.nih.gov/pubmed/31964130
http://dx.doi.org/10.5999/aps.2019.01529
_version_ 1783490370182578176
author Chung, Young Hun
Jang, Jin Woo
Cho, Jae Young
author_facet Chung, Young Hun
Jang, Jin Woo
Cho, Jae Young
author_sort Chung, Young Hun
collection PubMed
description Malignant peripheral nerve sheath tumor (MPNST) is a rare and often aggressive soft tissue sarcoma originating from the sheaths of peripheral nerves. Approximately 50% of MPNSTs occur in patients with neurofibromatosis (NF). These tumors often present as deep soft tissue lesions, arising from the nerve plexuses of the extremities or from the nerves extending from the trunk. They rarely occur in the skin, especially in patients with NF. Herein, we report our experience with an MPNST of the skin in a patient with NF.
format Online
Article
Text
id pubmed-6976743
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Korean Society of Plastic and Reconstructive Surgeons
record_format MEDLINE/PubMed
spelling pubmed-69767432020-02-04 Soft tissue sarcoma in neurofibromatosis type 1: A rare case of malignant peripheral nerve sheath tumor of the skin Chung, Young Hun Jang, Jin Woo Cho, Jae Young Arch Plast Surg Case Report Malignant peripheral nerve sheath tumor (MPNST) is a rare and often aggressive soft tissue sarcoma originating from the sheaths of peripheral nerves. Approximately 50% of MPNSTs occur in patients with neurofibromatosis (NF). These tumors often present as deep soft tissue lesions, arising from the nerve plexuses of the extremities or from the nerves extending from the trunk. They rarely occur in the skin, especially in patients with NF. Herein, we report our experience with an MPNST of the skin in a patient with NF. Korean Society of Plastic and Reconstructive Surgeons 2020-01 2020-01-15 /pmc/articles/PMC6976743/ /pubmed/31964130 http://dx.doi.org/10.5999/aps.2019.01529 Text en Copyright © 2020 The Korean Society of Plastic and Reconstructive Surgeons This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Chung, Young Hun
Jang, Jin Woo
Cho, Jae Young
Soft tissue sarcoma in neurofibromatosis type 1: A rare case of malignant peripheral nerve sheath tumor of the skin
title Soft tissue sarcoma in neurofibromatosis type 1: A rare case of malignant peripheral nerve sheath tumor of the skin
title_full Soft tissue sarcoma in neurofibromatosis type 1: A rare case of malignant peripheral nerve sheath tumor of the skin
title_fullStr Soft tissue sarcoma in neurofibromatosis type 1: A rare case of malignant peripheral nerve sheath tumor of the skin
title_full_unstemmed Soft tissue sarcoma in neurofibromatosis type 1: A rare case of malignant peripheral nerve sheath tumor of the skin
title_short Soft tissue sarcoma in neurofibromatosis type 1: A rare case of malignant peripheral nerve sheath tumor of the skin
title_sort soft tissue sarcoma in neurofibromatosis type 1: a rare case of malignant peripheral nerve sheath tumor of the skin
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6976743/
https://www.ncbi.nlm.nih.gov/pubmed/31964130
http://dx.doi.org/10.5999/aps.2019.01529
work_keys_str_mv AT chungyounghun softtissuesarcomainneurofibromatosistype1ararecaseofmalignantperipheralnervesheathtumoroftheskin
AT jangjinwoo softtissuesarcomainneurofibromatosistype1ararecaseofmalignantperipheralnervesheathtumoroftheskin
AT chojaeyoung softtissuesarcomainneurofibromatosistype1ararecaseofmalignantperipheralnervesheathtumoroftheskin