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Linear IgA disease in an adult with unusual clinical features
A 19-year-old male presented with complaints of fluid-filled lesions on the body of 2 weeks duration. On examination, he was found to have multiple tense bullae distributed on the flexures, face, and genitalia with associated oral ulcers and “cluster of jewels” sign. The diagnosis was confirmed by h...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3673376/ https://www.ncbi.nlm.nih.gov/pubmed/23741669 http://dx.doi.org/10.4103/2229-5178.110637 |
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author | Verma, Rajesh Vasudevan, Biju Pragasam, Vijendran Dabbas, Disha |
author_facet | Verma, Rajesh Vasudevan, Biju Pragasam, Vijendran Dabbas, Disha |
author_sort | Verma, Rajesh |
collection | PubMed |
description | A 19-year-old male presented with complaints of fluid-filled lesions on the body of 2 weeks duration. On examination, he was found to have multiple tense bullae distributed on the flexures, face, and genitalia with associated oral ulcers and “cluster of jewels” sign. The diagnosis was confirmed by histopathology and direct immunofluorescence. There are very few reports of linear IgA earlier from India according to the literature available so far, that too from the Southern part of the country. The patient had bullous pemphigoid-like lesions typically seen in adults, but the distribution of lesions was akin to that of the “chronic bullous disease of childhood variant” found in children. This case has been reported for rarity in this region and also because the patient had atypical morphology and distribution of lesions. |
format | Online Article Text |
id | pubmed-3673376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-36733762013-06-05 Linear IgA disease in an adult with unusual clinical features Verma, Rajesh Vasudevan, Biju Pragasam, Vijendran Dabbas, Disha Indian Dermatol Online J Case Report A 19-year-old male presented with complaints of fluid-filled lesions on the body of 2 weeks duration. On examination, he was found to have multiple tense bullae distributed on the flexures, face, and genitalia with associated oral ulcers and “cluster of jewels” sign. The diagnosis was confirmed by histopathology and direct immunofluorescence. There are very few reports of linear IgA earlier from India according to the literature available so far, that too from the Southern part of the country. The patient had bullous pemphigoid-like lesions typically seen in adults, but the distribution of lesions was akin to that of the “chronic bullous disease of childhood variant” found in children. This case has been reported for rarity in this region and also because the patient had atypical morphology and distribution of lesions. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3673376/ /pubmed/23741669 http://dx.doi.org/10.4103/2229-5178.110637 Text en Copyright: © Indian Dermatology Online Journal 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Verma, Rajesh Vasudevan, Biju Pragasam, Vijendran Dabbas, Disha Linear IgA disease in an adult with unusual clinical features |
title | Linear IgA disease in an adult with unusual clinical features |
title_full | Linear IgA disease in an adult with unusual clinical features |
title_fullStr | Linear IgA disease in an adult with unusual clinical features |
title_full_unstemmed | Linear IgA disease in an adult with unusual clinical features |
title_short | Linear IgA disease in an adult with unusual clinical features |
title_sort | linear iga disease in an adult with unusual clinical features |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3673376/ https://www.ncbi.nlm.nih.gov/pubmed/23741669 http://dx.doi.org/10.4103/2229-5178.110637 |
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