Coexistence of porokeratosis of Mibelli with Gardner's syndrome: A rare case report

Porokeratosis represents a heterogeneous group of disorders characterized clinically by a distinctive ridge-like border and histologically by cornoid lamellae. Gardner's syndrome, a variant of familial adenomatous polyposis (FAP), is an autosomal dominant disease characterized by colorectal pol...

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Autores principales: Ali, Syed Yousuf, Prabhat, Shivangi, Ramanamurty, Ch. V., Salma, Mahjabeen, Hussain, Shamshad, Murtaza, Ahmed Syed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications Pvt Ltd 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3481819/
https://www.ncbi.nlm.nih.gov/pubmed/23130235
http://dx.doi.org/10.4103/2229-5178.86001
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author Ali, Syed Yousuf
Prabhat, Shivangi
Ramanamurty, Ch. V.
Salma, Mahjabeen
Hussain, Shamshad
Murtaza, Ahmed Syed
author_facet Ali, Syed Yousuf
Prabhat, Shivangi
Ramanamurty, Ch. V.
Salma, Mahjabeen
Hussain, Shamshad
Murtaza, Ahmed Syed
author_sort Ali, Syed Yousuf
collection PubMed
description Porokeratosis represents a heterogeneous group of disorders characterized clinically by a distinctive ridge-like border and histologically by cornoid lamellae. Gardner's syndrome, a variant of familial adenomatous polyposis (FAP), is an autosomal dominant disease characterized by colorectal polyps, osteomas, epidermoid cysts and soft tissue tumors. Here we report a case of 18 yr old female who presented with porokeratosis of Mibelli with osteoma, multiple epidermoid cytsts, and solitary rectal polyp.
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spelling pubmed-34818192012-11-05 Coexistence of porokeratosis of Mibelli with Gardner's syndrome: A rare case report Ali, Syed Yousuf Prabhat, Shivangi Ramanamurty, Ch. V. Salma, Mahjabeen Hussain, Shamshad Murtaza, Ahmed Syed Indian Dermatol Online J Case Report Porokeratosis represents a heterogeneous group of disorders characterized clinically by a distinctive ridge-like border and histologically by cornoid lamellae. Gardner's syndrome, a variant of familial adenomatous polyposis (FAP), is an autosomal dominant disease characterized by colorectal polyps, osteomas, epidermoid cysts and soft tissue tumors. Here we report a case of 18 yr old female who presented with porokeratosis of Mibelli with osteoma, multiple epidermoid cytsts, and solitary rectal polyp. Medknow Publications Pvt Ltd 2011 /pmc/articles/PMC3481819/ /pubmed/23130235 http://dx.doi.org/10.4103/2229-5178.86001 Text en Copyright: © Indian Dermatology Online Journal 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
Ali, Syed Yousuf
Prabhat, Shivangi
Ramanamurty, Ch. V.
Salma, Mahjabeen
Hussain, Shamshad
Murtaza, Ahmed Syed
Coexistence of porokeratosis of Mibelli with Gardner's syndrome: A rare case report
title Coexistence of porokeratosis of Mibelli with Gardner's syndrome: A rare case report
title_full Coexistence of porokeratosis of Mibelli with Gardner's syndrome: A rare case report
title_fullStr Coexistence of porokeratosis of Mibelli with Gardner's syndrome: A rare case report
title_full_unstemmed Coexistence of porokeratosis of Mibelli with Gardner's syndrome: A rare case report
title_short Coexistence of porokeratosis of Mibelli with Gardner's syndrome: A rare case report
title_sort coexistence of porokeratosis of mibelli with gardner's syndrome: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3481819/
https://www.ncbi.nlm.nih.gov/pubmed/23130235
http://dx.doi.org/10.4103/2229-5178.86001
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