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Keratoacanthoma Centrifugum Marginatum with Spontaneous Regression and Its Possible Differential Diagnosis

Keratoacanthoma centrifugum marignatum (KCM) is a rare variant of keratoacanthoma, which is characterized by the dense infiltration of inflammatory cells throughout the dermis, especially around the keratinocytic islands. Therefore, it is sometimes difficult to differentiate between KCM and cutaneou...

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Autores principales: Amagai, Ryo, Fujimura, Taku, Kambayashi, Yumi, Furudate, Sadanori, Sato, Yota, Tanita, Kayo, Hashimoto, Akira, Aiba, Setsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244034/
https://www.ncbi.nlm.nih.gov/pubmed/30483096
http://dx.doi.org/10.1159/000493089
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author Amagai, Ryo
Fujimura, Taku
Kambayashi, Yumi
Furudate, Sadanori
Sato, Yota
Tanita, Kayo
Hashimoto, Akira
Aiba, Setsuya
author_facet Amagai, Ryo
Fujimura, Taku
Kambayashi, Yumi
Furudate, Sadanori
Sato, Yota
Tanita, Kayo
Hashimoto, Akira
Aiba, Setsuya
author_sort Amagai, Ryo
collection PubMed
description Keratoacanthoma centrifugum marignatum (KCM) is a rare variant of keratoacanthoma, which is characterized by the dense infiltration of inflammatory cells throughout the dermis, especially around the keratinocytic islands. Therefore, it is sometimes difficult to differentiate between KCM and cutaneous T-cell lymphomas. In this report, we describe a case of KCM with spontaneous regression that showed dense infiltration of CD3+CD8+ T cells. Our present case suggested the importance of investigating tumor-infiltrating lymphocytes to avoid the misdiagnosis of KCM as cutaneous T-cell lymphoma.
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spelling pubmed-62440342018-11-27 Keratoacanthoma Centrifugum Marginatum with Spontaneous Regression and Its Possible Differential Diagnosis Amagai, Ryo Fujimura, Taku Kambayashi, Yumi Furudate, Sadanori Sato, Yota Tanita, Kayo Hashimoto, Akira Aiba, Setsuya Case Rep Oncol Case Report Keratoacanthoma centrifugum marignatum (KCM) is a rare variant of keratoacanthoma, which is characterized by the dense infiltration of inflammatory cells throughout the dermis, especially around the keratinocytic islands. Therefore, it is sometimes difficult to differentiate between KCM and cutaneous T-cell lymphomas. In this report, we describe a case of KCM with spontaneous regression that showed dense infiltration of CD3+CD8+ T cells. Our present case suggested the importance of investigating tumor-infiltrating lymphocytes to avoid the misdiagnosis of KCM as cutaneous T-cell lymphoma. S. Karger AG 2018-10-24 /pmc/articles/PMC6244034/ /pubmed/30483096 http://dx.doi.org/10.1159/000493089 Text en Copyright © 2018 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 Case Report
Amagai, Ryo
Fujimura, Taku
Kambayashi, Yumi
Furudate, Sadanori
Sato, Yota
Tanita, Kayo
Hashimoto, Akira
Aiba, Setsuya
Keratoacanthoma Centrifugum Marginatum with Spontaneous Regression and Its Possible Differential Diagnosis
title Keratoacanthoma Centrifugum Marginatum with Spontaneous Regression and Its Possible Differential Diagnosis
title_full Keratoacanthoma Centrifugum Marginatum with Spontaneous Regression and Its Possible Differential Diagnosis
title_fullStr Keratoacanthoma Centrifugum Marginatum with Spontaneous Regression and Its Possible Differential Diagnosis
title_full_unstemmed Keratoacanthoma Centrifugum Marginatum with Spontaneous Regression and Its Possible Differential Diagnosis
title_short Keratoacanthoma Centrifugum Marginatum with Spontaneous Regression and Its Possible Differential Diagnosis
title_sort keratoacanthoma centrifugum marginatum with spontaneous regression and its possible differential diagnosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244034/
https://www.ncbi.nlm.nih.gov/pubmed/30483096
http://dx.doi.org/10.1159/000493089
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