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Keratoacanthoma Centrifugum Marginatum at an Unusual Site

Keratoacanthoma (KA) is a rapidly evolving tumor, composed of keratinizing squamous cells originating in pilosebaceous follicles and resolving spontaneously if left untreated. It is relatively uncommon in dark-skinned and occurs in middle aged individuals. Males are three times more affected than fe...

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Autores principales: Phiske, Meghana M, Avhad, Ganesh, Jerajani, HR
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3555381/
https://www.ncbi.nlm.nih.gov/pubmed/23372220
http://dx.doi.org/10.4103/0019-5154.105316
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author Phiske, Meghana M
Avhad, Ganesh
Jerajani, HR
author_facet Phiske, Meghana M
Avhad, Ganesh
Jerajani, HR
author_sort Phiske, Meghana M
collection PubMed
description Keratoacanthoma (KA) is a rapidly evolving tumor, composed of keratinizing squamous cells originating in pilosebaceous follicles and resolving spontaneously if left untreated. It is relatively uncommon in dark-skinned and occurs in middle aged individuals. Males are three times more affected than females. It presents as firm, rounded, flesh-colored or reddish papule; with a rapid growth phase followed by spontaneous healing over three months. Two types of KA exist i.e., solitary and multiple. There are three rare clinical variants of solitary KA, namely giant KA, keratoacanthoma centrifugum marginatum (KCM) and subungual KA. In KCM, lesions are large, reaching upto 20cms. There is peripheral extension with raised, rolled border and atrophy in the center. There is no tendency toward spontaneous involution. The most common locations are dorsa of hands and legs, lesions on scalp being rare. A rare case of KCM occurring on scalp which is an unusual site is reported.
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spelling pubmed-35553812013-01-31 Keratoacanthoma Centrifugum Marginatum at an Unusual Site Phiske, Meghana M Avhad, Ganesh Jerajani, HR Indian J Dermatol Case Report Keratoacanthoma (KA) is a rapidly evolving tumor, composed of keratinizing squamous cells originating in pilosebaceous follicles and resolving spontaneously if left untreated. It is relatively uncommon in dark-skinned and occurs in middle aged individuals. Males are three times more affected than females. It presents as firm, rounded, flesh-colored or reddish papule; with a rapid growth phase followed by spontaneous healing over three months. Two types of KA exist i.e., solitary and multiple. There are three rare clinical variants of solitary KA, namely giant KA, keratoacanthoma centrifugum marginatum (KCM) and subungual KA. In KCM, lesions are large, reaching upto 20cms. There is peripheral extension with raised, rolled border and atrophy in the center. There is no tendency toward spontaneous involution. The most common locations are dorsa of hands and legs, lesions on scalp being rare. A rare case of KCM occurring on scalp which is an unusual site is reported. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3555381/ /pubmed/23372220 http://dx.doi.org/10.4103/0019-5154.105316 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
Phiske, Meghana M
Avhad, Ganesh
Jerajani, HR
Keratoacanthoma Centrifugum Marginatum at an Unusual Site
title Keratoacanthoma Centrifugum Marginatum at an Unusual Site
title_full Keratoacanthoma Centrifugum Marginatum at an Unusual Site
title_fullStr Keratoacanthoma Centrifugum Marginatum at an Unusual Site
title_full_unstemmed Keratoacanthoma Centrifugum Marginatum at an Unusual Site
title_short Keratoacanthoma Centrifugum Marginatum at an Unusual Site
title_sort keratoacanthoma centrifugum marginatum at an unusual site
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3555381/
https://www.ncbi.nlm.nih.gov/pubmed/23372220
http://dx.doi.org/10.4103/0019-5154.105316
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