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Macular Amyloidosis and Epstein-Barr Virus

Background. Amyloidosis is extracellular precipitation of eosinophilic hyaline material of self-origin with special staining features and fibrillar ultrastructure. Macular amyloidosis is limited to the skin, and several factors have been proposed for its pathogenesis. Detection of Epstein-Barr virus...

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Autores principales: Nahidi, Yalda, Tayyebi Meibodi, Naser, Meshkat, Zahra, Nazeri, Narges
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4769766/
https://www.ncbi.nlm.nih.gov/pubmed/26981113
http://dx.doi.org/10.1155/2016/6089102
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author Nahidi, Yalda
Tayyebi Meibodi, Naser
Meshkat, Zahra
Nazeri, Narges
author_facet Nahidi, Yalda
Tayyebi Meibodi, Naser
Meshkat, Zahra
Nazeri, Narges
author_sort Nahidi, Yalda
collection PubMed
description Background. Amyloidosis is extracellular precipitation of eosinophilic hyaline material of self-origin with special staining features and fibrillar ultrastructure. Macular amyloidosis is limited to the skin, and several factors have been proposed for its pathogenesis. Detection of Epstein-Barr virus (EBV) DNA in this lesion suggests that this virus can play a role in pathogenesis of this disease. Objective. EBV DNA detection was done on 30 skin samples with a diagnosis of macular amyloidosis and 31 healthy skin samples in the margin of removed melanocytic nevi by using PCR. Results. In patients positive for beta-globin gene in PCR, BLLF1 gene of EBV virus was positive in 23 patients (8 patients in case and 15 patients in the control group). There was no significant difference in presence of EBV DNA between macular amyloidosis (3.8%) and control (23.8%) groups (P = 0.08). Conclusion. The findings of this study showed that EBV is not involved in pathogenesis of macular amyloidosis.
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spelling pubmed-47697662016-03-15 Macular Amyloidosis and Epstein-Barr Virus Nahidi, Yalda Tayyebi Meibodi, Naser Meshkat, Zahra Nazeri, Narges Dermatol Res Pract Research Article Background. Amyloidosis is extracellular precipitation of eosinophilic hyaline material of self-origin with special staining features and fibrillar ultrastructure. Macular amyloidosis is limited to the skin, and several factors have been proposed for its pathogenesis. Detection of Epstein-Barr virus (EBV) DNA in this lesion suggests that this virus can play a role in pathogenesis of this disease. Objective. EBV DNA detection was done on 30 skin samples with a diagnosis of macular amyloidosis and 31 healthy skin samples in the margin of removed melanocytic nevi by using PCR. Results. In patients positive for beta-globin gene in PCR, BLLF1 gene of EBV virus was positive in 23 patients (8 patients in case and 15 patients in the control group). There was no significant difference in presence of EBV DNA between macular amyloidosis (3.8%) and control (23.8%) groups (P = 0.08). Conclusion. The findings of this study showed that EBV is not involved in pathogenesis of macular amyloidosis. Hindawi Publishing Corporation 2016 2016-02-14 /pmc/articles/PMC4769766/ /pubmed/26981113 http://dx.doi.org/10.1155/2016/6089102 Text en Copyright © 2016 Yalda Nahidi et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Nahidi, Yalda
Tayyebi Meibodi, Naser
Meshkat, Zahra
Nazeri, Narges
Macular Amyloidosis and Epstein-Barr Virus
title Macular Amyloidosis and Epstein-Barr Virus
title_full Macular Amyloidosis and Epstein-Barr Virus
title_fullStr Macular Amyloidosis and Epstein-Barr Virus
title_full_unstemmed Macular Amyloidosis and Epstein-Barr Virus
title_short Macular Amyloidosis and Epstein-Barr Virus
title_sort macular amyloidosis and epstein-barr virus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4769766/
https://www.ncbi.nlm.nih.gov/pubmed/26981113
http://dx.doi.org/10.1155/2016/6089102
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