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Unilateral Multiple Facial Angiofibromas: A Case Report with Brief Review of Literature
Tuberous sclerosis (TSC) is an autosomal dominant hereditary condition with many varied forms of clinical presentation. The most frequent cutaneous findings in TSC include multiple angiofibromas, hypopigmented macules, periungual fibromas, and shagreen patch. Rarely, unilateral multiple facial angio...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3657241/ https://www.ncbi.nlm.nih.gov/pubmed/23716831 http://dx.doi.org/10.4103/0019-5154.108084 |
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author | Gutte, Rameshwar Khopkar, Uday |
author_facet | Gutte, Rameshwar Khopkar, Uday |
author_sort | Gutte, Rameshwar |
collection | PubMed |
description | Tuberous sclerosis (TSC) is an autosomal dominant hereditary condition with many varied forms of clinical presentation. The most frequent cutaneous findings in TSC include multiple angiofibromas, hypopigmented macules, periungual fibromas, and shagreen patch. Rarely, unilateral multiple facial angiofibromas have been reported. We report a case of unilateral multiple facial angiofibromas without any other manifestations of TSC. Although rare, unilateral multiple facial angiofibromas may be a mosaic form of TSC. |
format | Online Article Text |
id | pubmed-3657241 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-36572412013-05-28 Unilateral Multiple Facial Angiofibromas: A Case Report with Brief Review of Literature Gutte, Rameshwar Khopkar, Uday Indian J Dermatol E-Case Report Tuberous sclerosis (TSC) is an autosomal dominant hereditary condition with many varied forms of clinical presentation. The most frequent cutaneous findings in TSC include multiple angiofibromas, hypopigmented macules, periungual fibromas, and shagreen patch. Rarely, unilateral multiple facial angiofibromas have been reported. We report a case of unilateral multiple facial angiofibromas without any other manifestations of TSC. Although rare, unilateral multiple facial angiofibromas may be a mosaic form of TSC. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3657241/ /pubmed/23716831 http://dx.doi.org/10.4103/0019-5154.108084 Text en Copyright: © Indian Journal of Dermatology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | E-Case Report Gutte, Rameshwar Khopkar, Uday Unilateral Multiple Facial Angiofibromas: A Case Report with Brief Review of Literature |
title | Unilateral Multiple Facial Angiofibromas: A Case Report with Brief Review of Literature |
title_full | Unilateral Multiple Facial Angiofibromas: A Case Report with Brief Review of Literature |
title_fullStr | Unilateral Multiple Facial Angiofibromas: A Case Report with Brief Review of Literature |
title_full_unstemmed | Unilateral Multiple Facial Angiofibromas: A Case Report with Brief Review of Literature |
title_short | Unilateral Multiple Facial Angiofibromas: A Case Report with Brief Review of Literature |
title_sort | unilateral multiple facial angiofibromas: a case report with brief review of literature |
topic | E-Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3657241/ https://www.ncbi.nlm.nih.gov/pubmed/23716831 http://dx.doi.org/10.4103/0019-5154.108084 |
work_keys_str_mv | AT gutterameshwar unilateralmultiplefacialangiofibromasacasereportwithbriefreviewofliterature AT khopkaruday unilateralmultiplefacialangiofibromasacasereportwithbriefreviewofliterature |