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Oral migration of Dirofilaria repens after creeping dermatitis

We report an autochthonous case of oral dirofilariasis in a 46-year-old female patient exposed in South-Eastern France. The patient first presented eyelid creeping dermatitis of one-week duration, then a sub-mucosal nodule appeared in the cheek. The entire nodule was removed surgically. Histological...

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Detalles Bibliográficos
Autores principales: Hennocq, Quentin, Helary, Aloïs, Debelmas, Alexandre, Monsel, Gentiane, Labat, Amandine, Bertolus, Chloé, Martin, Coralie, Caumes, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: EDP Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7079549/
https://www.ncbi.nlm.nih.gov/pubmed/32186510
http://dx.doi.org/10.1051/parasite/2020015
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author Hennocq, Quentin
Helary, Aloïs
Debelmas, Alexandre
Monsel, Gentiane
Labat, Amandine
Bertolus, Chloé
Martin, Coralie
Caumes, Eric
author_facet Hennocq, Quentin
Helary, Aloïs
Debelmas, Alexandre
Monsel, Gentiane
Labat, Amandine
Bertolus, Chloé
Martin, Coralie
Caumes, Eric
author_sort Hennocq, Quentin
collection PubMed
description We report an autochthonous case of oral dirofilariasis in a 46-year-old female patient exposed in South-Eastern France. The patient first presented eyelid creeping dermatitis of one-week duration, then a sub-mucosal nodule appeared in the cheek. The entire nodule was removed surgically. Histologically, the nodule appeared as inflammatory tissue in which a worm was seen. The molecular analysis, based on cox1 and 12S sequences, identified Dirofilaria repens. Ivermectin treatment was given prior to diagnosis, while taking into consideration the most common causes of creeping dermatitis, but treatment was ineffective. The oral form of dirofilariasis is uncommon and could lead to diagnostic wandering.
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spelling pubmed-70795492020-03-25 Oral migration of Dirofilaria repens after creeping dermatitis Hennocq, Quentin Helary, Aloïs Debelmas, Alexandre Monsel, Gentiane Labat, Amandine Bertolus, Chloé Martin, Coralie Caumes, Eric Parasite Short Note We report an autochthonous case of oral dirofilariasis in a 46-year-old female patient exposed in South-Eastern France. The patient first presented eyelid creeping dermatitis of one-week duration, then a sub-mucosal nodule appeared in the cheek. The entire nodule was removed surgically. Histologically, the nodule appeared as inflammatory tissue in which a worm was seen. The molecular analysis, based on cox1 and 12S sequences, identified Dirofilaria repens. Ivermectin treatment was given prior to diagnosis, while taking into consideration the most common causes of creeping dermatitis, but treatment was ineffective. The oral form of dirofilariasis is uncommon and could lead to diagnostic wandering. EDP Sciences 2020-03-18 /pmc/articles/PMC7079549/ /pubmed/32186510 http://dx.doi.org/10.1051/parasite/2020015 Text en © Q. Hennocq et al., published by EDP Sciences, 2020 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Note
Hennocq, Quentin
Helary, Aloïs
Debelmas, Alexandre
Monsel, Gentiane
Labat, Amandine
Bertolus, Chloé
Martin, Coralie
Caumes, Eric
Oral migration of Dirofilaria repens after creeping dermatitis
title Oral migration of Dirofilaria repens after creeping dermatitis
title_full Oral migration of Dirofilaria repens after creeping dermatitis
title_fullStr Oral migration of Dirofilaria repens after creeping dermatitis
title_full_unstemmed Oral migration of Dirofilaria repens after creeping dermatitis
title_short Oral migration of Dirofilaria repens after creeping dermatitis
title_sort oral migration of dirofilaria repens after creeping dermatitis
topic Short Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7079549/
https://www.ncbi.nlm.nih.gov/pubmed/32186510
http://dx.doi.org/10.1051/parasite/2020015
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