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Dendritic cell distribution in mycosis fungoides vs. inflammatory dermatosis and other T-cell skin lymphoma

Dendritic cells (DCs) are antigen-presenting cells with an important role in the innate and adaptive immune system. In skin lesions, cutaneous DCs (Langerhans cells, dermal DCs and plasmacytoid DCs) are involved in immune activation in inflammatory benign lesions, as well as in malignant lymphoid pr...

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Autores principales: Cioplea, Mirela, Caruntu, Costin, Zurac, Sabina, Bastian, Alexandra, Sticlaru, Liana, Cioroianu, Alexandra, Boda, Daniel, Jugulete, Gheorghita, Nichita, Luciana, Popp, Cristiana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444333/
https://www.ncbi.nlm.nih.gov/pubmed/30944598
http://dx.doi.org/10.3892/ol.2019.10097
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author Cioplea, Mirela
Caruntu, Costin
Zurac, Sabina
Bastian, Alexandra
Sticlaru, Liana
Cioroianu, Alexandra
Boda, Daniel
Jugulete, Gheorghita
Nichita, Luciana
Popp, Cristiana
author_facet Cioplea, Mirela
Caruntu, Costin
Zurac, Sabina
Bastian, Alexandra
Sticlaru, Liana
Cioroianu, Alexandra
Boda, Daniel
Jugulete, Gheorghita
Nichita, Luciana
Popp, Cristiana
author_sort Cioplea, Mirela
collection PubMed
description Dendritic cells (DCs) are antigen-presenting cells with an important role in the innate and adaptive immune system. In skin lesions, cutaneous DCs (Langerhans cells, dermal DCs and plasmacytoid DCs) are involved in immune activation in inflammatory benign lesions, as well as in malignant lymphoid proliferations. Density and distribution of DCs in the dermal infiltrate can be helpful to differentiate benign, reactive infiltrate from malignant nature of the lymphoid population. We performed a retrospective study including 149 patients: 35 with mycosis fungoides, 35 with spongiotic dermatitis, 35 with psoriasis, 35 with lupus and 9 with cutaneous T-cell lymphomas (other than mycosis fungoides), diagnosed using histopathological and immunohistochemical stains. Density and distribution of DCs were evaluated using specific markers (CD1a, CD11c and langerin). In all cases, numerous DCs were identified in the dermal infiltrate. Their number was significantly increased in mycosis fungoides and T-cell lymphomas and moderately increased in inflammatory lesions. Variable patterns of distribution were identified such as clusters of DCs with arachnoid extension in mycosis fungoides, nodular pattern in inflammatory lesions and dispersed distribution with peripheric accumulation in T-skin lymphomas. Therefore, immunohistochemical characterization of DC distribution can be an adjuvant tool in differential diagnosis in inflammatory dermatosis and skin lymphomas.
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spelling pubmed-64443332019-04-03 Dendritic cell distribution in mycosis fungoides vs. inflammatory dermatosis and other T-cell skin lymphoma Cioplea, Mirela Caruntu, Costin Zurac, Sabina Bastian, Alexandra Sticlaru, Liana Cioroianu, Alexandra Boda, Daniel Jugulete, Gheorghita Nichita, Luciana Popp, Cristiana Oncol Lett Articles Dendritic cells (DCs) are antigen-presenting cells with an important role in the innate and adaptive immune system. In skin lesions, cutaneous DCs (Langerhans cells, dermal DCs and plasmacytoid DCs) are involved in immune activation in inflammatory benign lesions, as well as in malignant lymphoid proliferations. Density and distribution of DCs in the dermal infiltrate can be helpful to differentiate benign, reactive infiltrate from malignant nature of the lymphoid population. We performed a retrospective study including 149 patients: 35 with mycosis fungoides, 35 with spongiotic dermatitis, 35 with psoriasis, 35 with lupus and 9 with cutaneous T-cell lymphomas (other than mycosis fungoides), diagnosed using histopathological and immunohistochemical stains. Density and distribution of DCs were evaluated using specific markers (CD1a, CD11c and langerin). In all cases, numerous DCs were identified in the dermal infiltrate. Their number was significantly increased in mycosis fungoides and T-cell lymphomas and moderately increased in inflammatory lesions. Variable patterns of distribution were identified such as clusters of DCs with arachnoid extension in mycosis fungoides, nodular pattern in inflammatory lesions and dispersed distribution with peripheric accumulation in T-skin lymphomas. Therefore, immunohistochemical characterization of DC distribution can be an adjuvant tool in differential diagnosis in inflammatory dermatosis and skin lymphomas. D.A. Spandidos 2019-05 2019-03-01 /pmc/articles/PMC6444333/ /pubmed/30944598 http://dx.doi.org/10.3892/ol.2019.10097 Text en Copyright: © Cioplea et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Cioplea, Mirela
Caruntu, Costin
Zurac, Sabina
Bastian, Alexandra
Sticlaru, Liana
Cioroianu, Alexandra
Boda, Daniel
Jugulete, Gheorghita
Nichita, Luciana
Popp, Cristiana
Dendritic cell distribution in mycosis fungoides vs. inflammatory dermatosis and other T-cell skin lymphoma
title Dendritic cell distribution in mycosis fungoides vs. inflammatory dermatosis and other T-cell skin lymphoma
title_full Dendritic cell distribution in mycosis fungoides vs. inflammatory dermatosis and other T-cell skin lymphoma
title_fullStr Dendritic cell distribution in mycosis fungoides vs. inflammatory dermatosis and other T-cell skin lymphoma
title_full_unstemmed Dendritic cell distribution in mycosis fungoides vs. inflammatory dermatosis and other T-cell skin lymphoma
title_short Dendritic cell distribution in mycosis fungoides vs. inflammatory dermatosis and other T-cell skin lymphoma
title_sort dendritic cell distribution in mycosis fungoides vs. inflammatory dermatosis and other t-cell skin lymphoma
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444333/
https://www.ncbi.nlm.nih.gov/pubmed/30944598
http://dx.doi.org/10.3892/ol.2019.10097
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