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Granulocytic Spongiotic Papulovesiculosis (Neutrophilic Spongiosis): A Rare Entity
Neutrophilic spongiosis also known as granulocytic spongiotic papulovesiculosis (GSPV) is an uncommon disorder of uncertain classification. We report the case of a 45-year-old woman suffering from recurrent episodes of itchy, grouped papulovesicles over her body, histologically showing granulocytic...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5286760/ https://www.ncbi.nlm.nih.gov/pubmed/28216731 http://dx.doi.org/10.4103/0019-5154.198038 |
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author | Mendiratta, Vibhu Sanke, Sarita Ramchander, Nangia, Anita |
author_facet | Mendiratta, Vibhu Sanke, Sarita Ramchander, Nangia, Anita |
author_sort | Mendiratta, Vibhu |
collection | PubMed |
description | Neutrophilic spongiosis also known as granulocytic spongiotic papulovesiculosis (GSPV) is an uncommon disorder of uncertain classification. We report the case of a 45-year-old woman suffering from recurrent episodes of itchy, grouped papulovesicles over her body, histologically showing granulocytic spongiosis. The eruptions showed complete response to dapsone. |
format | Online Article Text |
id | pubmed-5286760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-52867602017-02-17 Granulocytic Spongiotic Papulovesiculosis (Neutrophilic Spongiosis): A Rare Entity Mendiratta, Vibhu Sanke, Sarita Ramchander, Nangia, Anita Indian J Dermatol Case Report Neutrophilic spongiosis also known as granulocytic spongiotic papulovesiculosis (GSPV) is an uncommon disorder of uncertain classification. We report the case of a 45-year-old woman suffering from recurrent episodes of itchy, grouped papulovesicles over her body, histologically showing granulocytic spongiosis. The eruptions showed complete response to dapsone. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5286760/ /pubmed/28216731 http://dx.doi.org/10.4103/0019-5154.198038 Text en Copyright: © 2017 Indian Journal of Dermatology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Mendiratta, Vibhu Sanke, Sarita Ramchander, Nangia, Anita Granulocytic Spongiotic Papulovesiculosis (Neutrophilic Spongiosis): A Rare Entity |
title | Granulocytic Spongiotic Papulovesiculosis (Neutrophilic Spongiosis): A Rare Entity |
title_full | Granulocytic Spongiotic Papulovesiculosis (Neutrophilic Spongiosis): A Rare Entity |
title_fullStr | Granulocytic Spongiotic Papulovesiculosis (Neutrophilic Spongiosis): A Rare Entity |
title_full_unstemmed | Granulocytic Spongiotic Papulovesiculosis (Neutrophilic Spongiosis): A Rare Entity |
title_short | Granulocytic Spongiotic Papulovesiculosis (Neutrophilic Spongiosis): A Rare Entity |
title_sort | granulocytic spongiotic papulovesiculosis (neutrophilic spongiosis): a rare entity |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5286760/ https://www.ncbi.nlm.nih.gov/pubmed/28216731 http://dx.doi.org/10.4103/0019-5154.198038 |
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