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Acquired Cutis Laxa Associated with Light and Heavy Chain Deposition Disease
Acquired cutis laxa (ACL) is a rare connective tissue disorder characterized by pendulous and coarsely wrinkled skin. There have been few cases of its association to monoclonal immunoglobulin deposition disease (MIDD), which constitutes the light chain (LCDD), heavy chain (HCDD), and light and heavy...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5803942/ https://www.ncbi.nlm.nih.gov/pubmed/29441298 http://dx.doi.org/10.4103/idoj.IDOJ_403_16 |
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author | Majithia, Reena A. George, Leni Thomas, Meera Fouzia, N. A. |
author_facet | Majithia, Reena A. George, Leni Thomas, Meera Fouzia, N. A. |
author_sort | Majithia, Reena A. |
collection | PubMed |
description | Acquired cutis laxa (ACL) is a rare connective tissue disorder characterized by pendulous and coarsely wrinkled skin. There have been few cases of its association to monoclonal immunoglobulin deposition disease (MIDD), which constitutes the light chain (LCDD), heavy chain (HCDD), and light and heavy chain (LHCDD) deposition disease. MIDD predominantly involves the kidney. Skin is the next common organ to be affected by HCDD, which presents as ACL. We report the case of a 40-year-old male who presented with ACL associated with LHCDD. The clinical features of ACL in the present case appeared prior to the development of clinical features related to LHCDD. |
format | Online Article Text |
id | pubmed-5803942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-58039422018-02-13 Acquired Cutis Laxa Associated with Light and Heavy Chain Deposition Disease Majithia, Reena A. George, Leni Thomas, Meera Fouzia, N. A. Indian Dermatol Online J Case Report Acquired cutis laxa (ACL) is a rare connective tissue disorder characterized by pendulous and coarsely wrinkled skin. There have been few cases of its association to monoclonal immunoglobulin deposition disease (MIDD), which constitutes the light chain (LCDD), heavy chain (HCDD), and light and heavy chain (LHCDD) deposition disease. MIDD predominantly involves the kidney. Skin is the next common organ to be affected by HCDD, which presents as ACL. We report the case of a 40-year-old male who presented with ACL associated with LHCDD. The clinical features of ACL in the present case appeared prior to the development of clinical features related to LHCDD. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC5803942/ /pubmed/29441298 http://dx.doi.org/10.4103/idoj.IDOJ_403_16 Text en Copyright: © 2018 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-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 Majithia, Reena A. George, Leni Thomas, Meera Fouzia, N. A. Acquired Cutis Laxa Associated with Light and Heavy Chain Deposition Disease |
title | Acquired Cutis Laxa Associated with Light and Heavy Chain Deposition Disease |
title_full | Acquired Cutis Laxa Associated with Light and Heavy Chain Deposition Disease |
title_fullStr | Acquired Cutis Laxa Associated with Light and Heavy Chain Deposition Disease |
title_full_unstemmed | Acquired Cutis Laxa Associated with Light and Heavy Chain Deposition Disease |
title_short | Acquired Cutis Laxa Associated with Light and Heavy Chain Deposition Disease |
title_sort | acquired cutis laxa associated with light and heavy chain deposition disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5803942/ https://www.ncbi.nlm.nih.gov/pubmed/29441298 http://dx.doi.org/10.4103/idoj.IDOJ_403_16 |
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