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Malignant Peripheral Nerve Sheath Tumor of the Inguinum and Angiosarcoma of the Scalp in a Child with Neurofibromatosis Type 1
Benign and malignant tumors are common in the setting of neurofibromatosis type 1 (NF1). Malignant peripheral nerve sheath tumor (MPNST) and angiosarcoma are rare tumors in children and adolescents and mostly occur in young patients in relation to NF1. Both histological types can be present in the s...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613689/ https://www.ncbi.nlm.nih.gov/pubmed/29138703 http://dx.doi.org/10.1155/2017/7542825 |
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author | Milković Periša, Marija Džombeta, Tihana Stepan Giljević, Jasminka Krušlin, Božo |
author_facet | Milković Periša, Marija Džombeta, Tihana Stepan Giljević, Jasminka Krušlin, Božo |
author_sort | Milković Periša, Marija |
collection | PubMed |
description | Benign and malignant tumors are common in the setting of neurofibromatosis type 1 (NF1). Malignant peripheral nerve sheath tumor (MPNST) and angiosarcoma are rare tumors in children and adolescents and mostly occur in young patients in relation to NF1. Both histological types can be present in the same tumor mass in patients with NF1. We present a case of 12.5-year-old girl with NF1 who first presented with MPNST of the right inguinal region and 1.5 years later with unrelated angiosarcoma of the scalp. |
format | Online Article Text |
id | pubmed-5613689 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-56136892017-11-14 Malignant Peripheral Nerve Sheath Tumor of the Inguinum and Angiosarcoma of the Scalp in a Child with Neurofibromatosis Type 1 Milković Periša, Marija Džombeta, Tihana Stepan Giljević, Jasminka Krušlin, Božo Case Rep Pathol Case Report Benign and malignant tumors are common in the setting of neurofibromatosis type 1 (NF1). Malignant peripheral nerve sheath tumor (MPNST) and angiosarcoma are rare tumors in children and adolescents and mostly occur in young patients in relation to NF1. Both histological types can be present in the same tumor mass in patients with NF1. We present a case of 12.5-year-old girl with NF1 who first presented with MPNST of the right inguinal region and 1.5 years later with unrelated angiosarcoma of the scalp. Hindawi 2017 2017-08-24 /pmc/articles/PMC5613689/ /pubmed/29138703 http://dx.doi.org/10.1155/2017/7542825 Text en Copyright © 2017 Marija Milković Periša et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Milković Periša, Marija Džombeta, Tihana Stepan Giljević, Jasminka Krušlin, Božo Malignant Peripheral Nerve Sheath Tumor of the Inguinum and Angiosarcoma of the Scalp in a Child with Neurofibromatosis Type 1 |
title | Malignant Peripheral Nerve Sheath Tumor of the Inguinum and Angiosarcoma of the Scalp in a Child with Neurofibromatosis Type 1 |
title_full | Malignant Peripheral Nerve Sheath Tumor of the Inguinum and Angiosarcoma of the Scalp in a Child with Neurofibromatosis Type 1 |
title_fullStr | Malignant Peripheral Nerve Sheath Tumor of the Inguinum and Angiosarcoma of the Scalp in a Child with Neurofibromatosis Type 1 |
title_full_unstemmed | Malignant Peripheral Nerve Sheath Tumor of the Inguinum and Angiosarcoma of the Scalp in a Child with Neurofibromatosis Type 1 |
title_short | Malignant Peripheral Nerve Sheath Tumor of the Inguinum and Angiosarcoma of the Scalp in a Child with Neurofibromatosis Type 1 |
title_sort | malignant peripheral nerve sheath tumor of the inguinum and angiosarcoma of the scalp in a child with neurofibromatosis type 1 |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613689/ https://www.ncbi.nlm.nih.gov/pubmed/29138703 http://dx.doi.org/10.1155/2017/7542825 |
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