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A Rare Case of a Symptomatic Tumor Found in the Groin Area: An Atypical Location Unexposed to the Known Causes
Nevoid basal cell carcinoma syndrome (NBCCS), also known as Gorlin syndrome, is a rare hereditary condition characterized by a wide range of developmental abnormalities and a predisposition to neoplasms. The syndrome consists of early-onset and/or multiple BCC. Herein we report a rare NBCCS case in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787896/ https://www.ncbi.nlm.nih.gov/pubmed/26997948 http://dx.doi.org/10.1159/000442148 |
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author | Toyonaga, Ellen Hata, Hiroo Nakayama, Chihiro Homma, Erina Miyashita, Toshiyuki Shimizu, Hiroshi |
author_facet | Toyonaga, Ellen Hata, Hiroo Nakayama, Chihiro Homma, Erina Miyashita, Toshiyuki Shimizu, Hiroshi |
author_sort | Toyonaga, Ellen |
collection | PubMed |
description | Nevoid basal cell carcinoma syndrome (NBCCS), also known as Gorlin syndrome, is a rare hereditary condition characterized by a wide range of developmental abnormalities and a predisposition to neoplasms. The syndrome consists of early-onset and/or multiple BCC. Herein we report a rare NBCCS case in which the first BCC onset occurred in the groin area. To the best of our knowledge, there have been no reports of first-onset BCC in the groin area in an NBCCS patient of any race. |
format | Online Article Text |
id | pubmed-4787896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-47878962016-03-18 A Rare Case of a Symptomatic Tumor Found in the Groin Area: An Atypical Location Unexposed to the Known Causes Toyonaga, Ellen Hata, Hiroo Nakayama, Chihiro Homma, Erina Miyashita, Toshiyuki Shimizu, Hiroshi Case Rep Oncol Published online: November, 2015 Nevoid basal cell carcinoma syndrome (NBCCS), also known as Gorlin syndrome, is a rare hereditary condition characterized by a wide range of developmental abnormalities and a predisposition to neoplasms. The syndrome consists of early-onset and/or multiple BCC. Herein we report a rare NBCCS case in which the first BCC onset occurred in the groin area. To the best of our knowledge, there have been no reports of first-onset BCC in the groin area in an NBCCS patient of any race. S. Karger AG 2015-11-27 /pmc/articles/PMC4787896/ /pubmed/26997948 http://dx.doi.org/10.1159/000442148 Text en Copyright © 2015 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission. |
spellingShingle | Published online: November, 2015 Toyonaga, Ellen Hata, Hiroo Nakayama, Chihiro Homma, Erina Miyashita, Toshiyuki Shimizu, Hiroshi A Rare Case of a Symptomatic Tumor Found in the Groin Area: An Atypical Location Unexposed to the Known Causes |
title | A Rare Case of a Symptomatic Tumor Found in the Groin Area: An Atypical Location Unexposed to the Known Causes |
title_full | A Rare Case of a Symptomatic Tumor Found in the Groin Area: An Atypical Location Unexposed to the Known Causes |
title_fullStr | A Rare Case of a Symptomatic Tumor Found in the Groin Area: An Atypical Location Unexposed to the Known Causes |
title_full_unstemmed | A Rare Case of a Symptomatic Tumor Found in the Groin Area: An Atypical Location Unexposed to the Known Causes |
title_short | A Rare Case of a Symptomatic Tumor Found in the Groin Area: An Atypical Location Unexposed to the Known Causes |
title_sort | rare case of a symptomatic tumor found in the groin area: an atypical location unexposed to the known causes |
topic | Published online: November, 2015 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787896/ https://www.ncbi.nlm.nih.gov/pubmed/26997948 http://dx.doi.org/10.1159/000442148 |
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