Multiple Familial Trichoepithelioma with an Adjacent Basal Cell Carcinoma, Transformation or Collision – A Case Report and Review of Literature

Trichoepithelioma is a benign tumor of follicular origin that presents as small, skin-colored papules predominantly on the face. When more than one family member is affected, the disease is known as multiple familial trichoepithelioma (MFT). It is a rare autosomal dominant skin disease. Malignant tr...

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Autores principales: Sangwaiya, Ashok, Sharma, Jyoti, Sharma, Swati, Munghate, Anand, Samal, Swagatika, Sen, Rajeev
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4458941/
https://www.ncbi.nlm.nih.gov/pubmed/26120156
http://dx.doi.org/10.4103/0019-5154.156380
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author Sangwaiya, Ashok
Sharma, Jyoti
Sharma, Swati
Munghate, Anand
Samal, Swagatika
Sen, Rajeev
author_facet Sangwaiya, Ashok
Sharma, Jyoti
Sharma, Swati
Munghate, Anand
Samal, Swagatika
Sen, Rajeev
author_sort Sangwaiya, Ashok
collection PubMed
description Trichoepithelioma is a benign tumor of follicular origin that presents as small, skin-colored papules predominantly on the face. When more than one family member is affected, the disease is known as multiple familial trichoepithelioma (MFT). It is a rare autosomal dominant skin disease. Malignant transformation is very rare. We describe here a case that developed malignant neoplasm in a setting of multiple trichoepithelioma.
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spelling pubmed-44589412015-06-26 Multiple Familial Trichoepithelioma with an Adjacent Basal Cell Carcinoma, Transformation or Collision – A Case Report and Review of Literature Sangwaiya, Ashok Sharma, Jyoti Sharma, Swati Munghate, Anand Samal, Swagatika Sen, Rajeev Indian J Dermatol Case Report Trichoepithelioma is a benign tumor of follicular origin that presents as small, skin-colored papules predominantly on the face. When more than one family member is affected, the disease is known as multiple familial trichoepithelioma (MFT). It is a rare autosomal dominant skin disease. Malignant transformation is very rare. We describe here a case that developed malignant neoplasm in a setting of multiple trichoepithelioma. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4458941/ /pubmed/26120156 http://dx.doi.org/10.4103/0019-5154.156380 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 Case Report
Sangwaiya, Ashok
Sharma, Jyoti
Sharma, Swati
Munghate, Anand
Samal, Swagatika
Sen, Rajeev
Multiple Familial Trichoepithelioma with an Adjacent Basal Cell Carcinoma, Transformation or Collision – A Case Report and Review of Literature
title Multiple Familial Trichoepithelioma with an Adjacent Basal Cell Carcinoma, Transformation or Collision – A Case Report and Review of Literature
title_full Multiple Familial Trichoepithelioma with an Adjacent Basal Cell Carcinoma, Transformation or Collision – A Case Report and Review of Literature
title_fullStr Multiple Familial Trichoepithelioma with an Adjacent Basal Cell Carcinoma, Transformation or Collision – A Case Report and Review of Literature
title_full_unstemmed Multiple Familial Trichoepithelioma with an Adjacent Basal Cell Carcinoma, Transformation or Collision – A Case Report and Review of Literature
title_short Multiple Familial Trichoepithelioma with an Adjacent Basal Cell Carcinoma, Transformation or Collision – A Case Report and Review of Literature
title_sort multiple familial trichoepithelioma with an adjacent basal cell carcinoma, transformation or collision – a case report and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4458941/
https://www.ncbi.nlm.nih.gov/pubmed/26120156
http://dx.doi.org/10.4103/0019-5154.156380
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