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Skin lesions caused by Orthopoxvirus in children
INTRODUCTION: The global eradication of smallpox and abandonment of mandatory smallpox vaccination has led to an increased proportion of the population who are immunologically naïve to infections caused by Orthopoxviruses (OPV). AIM: To present the different courses of OPV infection in children and...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7675095/ https://www.ncbi.nlm.nih.gov/pubmed/33240008 http://dx.doi.org/10.5114/ada.2019.85366 |
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author | Mazur-Melewska, Katarzyna Pieczonka-Ruszkowska, Ilona Szpura, Krystyna Myszkowska-Torz, Agnieszka Mania, Anna Kemnitz, Paweł Służewski, Wojciech Figlerowicz, Magdalena |
author_facet | Mazur-Melewska, Katarzyna Pieczonka-Ruszkowska, Ilona Szpura, Krystyna Myszkowska-Torz, Agnieszka Mania, Anna Kemnitz, Paweł Służewski, Wojciech Figlerowicz, Magdalena |
author_sort | Mazur-Melewska, Katarzyna |
collection | PubMed |
description | INTRODUCTION: The global eradication of smallpox and abandonment of mandatory smallpox vaccination has led to an increased proportion of the population who are immunologically naïve to infections caused by Orthopoxviruses (OPV). AIM: To present the different courses of OPV infection in children and to highlight the diagnostic difficulties in their differentiation from the other inflammatory processes. MATERIAL AND METHODS: We retrospectively evaluated the medical documentation of 5 children with OPV infection. Clinical diagnosis of OPV infection was based on evaluation of animal contact and skin symptoms, characterised by either a single ulcer or disseminated lesions. In all five cases, blood samples and skin swabs were collected from the lesion(s) to identify specific OPV DNA fragments (Vgf, b9R and D11L genes) using PCR. RESULTS: Two children presented with high fever, a single ulcer on the skin and local lymphadenopathy. The three other patients were in good general health and their skin lesions presented as a disseminated vesicular rash. Using the Vgf gene as the target for PCR, OPV infection was confirmed in material collected from skin lesions of all children and in blood samples of 4 children. The B9R and d11L genes tested positive in the skin material of 2 children and blood samples of 2 children. All analysed patients presented a history of ineffective antibiotic therapy. CONCLUSIONS: In the case of unclear necrotising skin lesions in children, the primary diagnosis always includes bacterial dermatitis. However, if the patient has come into contact with animals, diagnosis of OPV infection should also be considered. |
format | Online Article Text |
id | pubmed-7675095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-76750952020-11-24 Skin lesions caused by Orthopoxvirus in children Mazur-Melewska, Katarzyna Pieczonka-Ruszkowska, Ilona Szpura, Krystyna Myszkowska-Torz, Agnieszka Mania, Anna Kemnitz, Paweł Służewski, Wojciech Figlerowicz, Magdalena Postepy Dermatol Alergol Original Paper INTRODUCTION: The global eradication of smallpox and abandonment of mandatory smallpox vaccination has led to an increased proportion of the population who are immunologically naïve to infections caused by Orthopoxviruses (OPV). AIM: To present the different courses of OPV infection in children and to highlight the diagnostic difficulties in their differentiation from the other inflammatory processes. MATERIAL AND METHODS: We retrospectively evaluated the medical documentation of 5 children with OPV infection. Clinical diagnosis of OPV infection was based on evaluation of animal contact and skin symptoms, characterised by either a single ulcer or disseminated lesions. In all five cases, blood samples and skin swabs were collected from the lesion(s) to identify specific OPV DNA fragments (Vgf, b9R and D11L genes) using PCR. RESULTS: Two children presented with high fever, a single ulcer on the skin and local lymphadenopathy. The three other patients were in good general health and their skin lesions presented as a disseminated vesicular rash. Using the Vgf gene as the target for PCR, OPV infection was confirmed in material collected from skin lesions of all children and in blood samples of 4 children. The B9R and d11L genes tested positive in the skin material of 2 children and blood samples of 2 children. All analysed patients presented a history of ineffective antibiotic therapy. CONCLUSIONS: In the case of unclear necrotising skin lesions in children, the primary diagnosis always includes bacterial dermatitis. However, if the patient has come into contact with animals, diagnosis of OPV infection should also be considered. Termedia Publishing House 2019-08-22 2020-10 /pmc/articles/PMC7675095/ /pubmed/33240008 http://dx.doi.org/10.5114/ada.2019.85366 Text en Copyright © 2020 Termedia http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0). License (http://creativecommons.org/licenses/by-nc-sa/4.0/) |
spellingShingle | Original Paper Mazur-Melewska, Katarzyna Pieczonka-Ruszkowska, Ilona Szpura, Krystyna Myszkowska-Torz, Agnieszka Mania, Anna Kemnitz, Paweł Służewski, Wojciech Figlerowicz, Magdalena Skin lesions caused by Orthopoxvirus in children |
title | Skin lesions caused by Orthopoxvirus in children |
title_full | Skin lesions caused by Orthopoxvirus in children |
title_fullStr | Skin lesions caused by Orthopoxvirus in children |
title_full_unstemmed | Skin lesions caused by Orthopoxvirus in children |
title_short | Skin lesions caused by Orthopoxvirus in children |
title_sort | skin lesions caused by orthopoxvirus in children |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7675095/ https://www.ncbi.nlm.nih.gov/pubmed/33240008 http://dx.doi.org/10.5114/ada.2019.85366 |
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