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Reverse Koebner Phenomenon in Bullous Pemphigoid – A Case Report

Reverse Koebner response is the nonappearance or disappearance of the lesions of particular dermatoses at the site of injury. Herein we report a case of the reverse Koebner phenomenon in bullous pemphigoid in a 35-year-old male patient with sparing of the waist area which could probably be because o...

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Autores principales: Mohapatra, Liza, Samal, Kallolinee, Mohanty, Prasenjeet, Dash, Siddhartha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859752/
https://www.ncbi.nlm.nih.gov/pubmed/31807450
http://dx.doi.org/10.4103/idoj.IDOJ_512_18
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author Mohapatra, Liza
Samal, Kallolinee
Mohanty, Prasenjeet
Dash, Siddhartha
author_facet Mohapatra, Liza
Samal, Kallolinee
Mohanty, Prasenjeet
Dash, Siddhartha
author_sort Mohapatra, Liza
collection PubMed
description Reverse Koebner response is the nonappearance or disappearance of the lesions of particular dermatoses at the site of injury. Herein we report a case of the reverse Koebner phenomenon in bullous pemphigoid in a 35-year-old male patient with sparing of the waist area which could probably be because of the phenomenon of locus majoris resistentiae. The histopathology of the lesion showed subepidermal split with a mixed inflammatory infiltrate, which was composed of predominantly eosinophils, neutrophils, and lymphocytes, but the histopathology of the spared skin showed no abnormalities. However, the direct immunofluorescence from the perilesional area showed linear deposits of immunoglobulin G and C3 in the dermoepidermal junction, but there were no deposits in direct immunofluorescence from the spared skin. This case is being reported for its originality and one of its kind.
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spelling pubmed-68597522019-12-05 Reverse Koebner Phenomenon in Bullous Pemphigoid – A Case Report Mohapatra, Liza Samal, Kallolinee Mohanty, Prasenjeet Dash, Siddhartha Indian Dermatol Online J Case Report Reverse Koebner response is the nonappearance or disappearance of the lesions of particular dermatoses at the site of injury. Herein we report a case of the reverse Koebner phenomenon in bullous pemphigoid in a 35-year-old male patient with sparing of the waist area which could probably be because of the phenomenon of locus majoris resistentiae. The histopathology of the lesion showed subepidermal split with a mixed inflammatory infiltrate, which was composed of predominantly eosinophils, neutrophils, and lymphocytes, but the histopathology of the spared skin showed no abnormalities. However, the direct immunofluorescence from the perilesional area showed linear deposits of immunoglobulin G and C3 in the dermoepidermal junction, but there were no deposits in direct immunofluorescence from the spared skin. This case is being reported for its originality and one of its kind. Wolters Kluwer - Medknow 2019-11-01 /pmc/articles/PMC6859752/ /pubmed/31807450 http://dx.doi.org/10.4103/idoj.IDOJ_512_18 Text en Copyright: © 2019 Indian Dermatology Online Journal http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Mohapatra, Liza
Samal, Kallolinee
Mohanty, Prasenjeet
Dash, Siddhartha
Reverse Koebner Phenomenon in Bullous Pemphigoid – A Case Report
title Reverse Koebner Phenomenon in Bullous Pemphigoid – A Case Report
title_full Reverse Koebner Phenomenon in Bullous Pemphigoid – A Case Report
title_fullStr Reverse Koebner Phenomenon in Bullous Pemphigoid – A Case Report
title_full_unstemmed Reverse Koebner Phenomenon in Bullous Pemphigoid – A Case Report
title_short Reverse Koebner Phenomenon in Bullous Pemphigoid – A Case Report
title_sort reverse koebner phenomenon in bullous pemphigoid – a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859752/
https://www.ncbi.nlm.nih.gov/pubmed/31807450
http://dx.doi.org/10.4103/idoj.IDOJ_512_18
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