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Congenital Cutaneous Peripheral Primitive Neuroectodermal Tumor (pPNET) of Scalp: Youngest Case So Far
Congenital cutaneous peripheral primitive neuroectodermal tumor (pPNET) is very rare and also very rarely located in scalp. Only two cases of PNET as primary tumor in scalp are reported so far in the literature. Non mutilating surgical excision, combined with chemotherapy and radiotherapy are used i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8074827/ https://www.ncbi.nlm.nih.gov/pubmed/33953517 http://dx.doi.org/10.4103/jiaps.JIAPS_68_20 |
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author | Kumar, Parveen Panda, Shasanka Shekhar Singh, Sarika Sarin, Yogesh Kumar |
author_facet | Kumar, Parveen Panda, Shasanka Shekhar Singh, Sarika Sarin, Yogesh Kumar |
author_sort | Kumar, Parveen |
collection | PubMed |
description | Congenital cutaneous peripheral primitive neuroectodermal tumor (pPNET) is very rare and also very rarely located in scalp. Only two cases of PNET as primary tumor in scalp are reported so far in the literature. Non mutilating surgical excision, combined with chemotherapy and radiotherapy are used in treating these rare tumors. We present the youngest case report of PNET of scalp in 10-month-old girl who was managed by surgical excision with good cosmetic outcome and disease-free 20 months post-operative period. |
format | Online Article Text |
id | pubmed-8074827 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-80748272021-05-04 Congenital Cutaneous Peripheral Primitive Neuroectodermal Tumor (pPNET) of Scalp: Youngest Case So Far Kumar, Parveen Panda, Shasanka Shekhar Singh, Sarika Sarin, Yogesh Kumar J Indian Assoc Pediatr Surg Case Report Congenital cutaneous peripheral primitive neuroectodermal tumor (pPNET) is very rare and also very rarely located in scalp. Only two cases of PNET as primary tumor in scalp are reported so far in the literature. Non mutilating surgical excision, combined with chemotherapy and radiotherapy are used in treating these rare tumors. We present the youngest case report of PNET of scalp in 10-month-old girl who was managed by surgical excision with good cosmetic outcome and disease-free 20 months post-operative period. Wolters Kluwer - Medknow 2021 2021-01-11 /pmc/articles/PMC8074827/ /pubmed/33953517 http://dx.doi.org/10.4103/jiaps.JIAPS_68_20 Text en Copyright: © 2021 Journal of Indian Association of Pediatric Surgeons https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Kumar, Parveen Panda, Shasanka Shekhar Singh, Sarika Sarin, Yogesh Kumar Congenital Cutaneous Peripheral Primitive Neuroectodermal Tumor (pPNET) of Scalp: Youngest Case So Far |
title | Congenital Cutaneous Peripheral Primitive Neuroectodermal Tumor (pPNET) of Scalp: Youngest Case So Far |
title_full | Congenital Cutaneous Peripheral Primitive Neuroectodermal Tumor (pPNET) of Scalp: Youngest Case So Far |
title_fullStr | Congenital Cutaneous Peripheral Primitive Neuroectodermal Tumor (pPNET) of Scalp: Youngest Case So Far |
title_full_unstemmed | Congenital Cutaneous Peripheral Primitive Neuroectodermal Tumor (pPNET) of Scalp: Youngest Case So Far |
title_short | Congenital Cutaneous Peripheral Primitive Neuroectodermal Tumor (pPNET) of Scalp: Youngest Case So Far |
title_sort | congenital cutaneous peripheral primitive neuroectodermal tumor (ppnet) of scalp: youngest case so far |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8074827/ https://www.ncbi.nlm.nih.gov/pubmed/33953517 http://dx.doi.org/10.4103/jiaps.JIAPS_68_20 |
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