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Amalgam Contact Hypersensitivity Lesion: An Unusual Presentation-Report Of A Rare Case

Amalgam or its components may cause Type IV hypersensitivity reactions on the oral mucosa. These amalgam contact hypersensitivity lesions (ACHL) present as white striae and plaques, erythematous, erosive, atrophic, or ulcerative lesions. Postinflammatory pigmentation in such lesions and pigmentation...

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Detalles Bibliográficos
Autores principales: Ramnarayan, BK, Maligi, PM, Smitha, T, Patil, US
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4212399/
https://www.ncbi.nlm.nih.gov/pubmed/25364611
http://dx.doi.org/10.4103/2141-9248.141981
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author Ramnarayan, BK
Maligi, PM
Smitha, T
Patil, US
author_facet Ramnarayan, BK
Maligi, PM
Smitha, T
Patil, US
author_sort Ramnarayan, BK
collection PubMed
description Amalgam or its components may cause Type IV hypersensitivity reactions on the oral mucosa. These amalgam contact hypersensitivity lesions (ACHL) present as white striae and plaques, erythematous, erosive, atrophic, or ulcerative lesions. Postinflammatory pigmentation in such lesions and pigmentation due to amalgam incorporation in the soft tissue have been reported in the literature. However, ACHL presenting primarily as a black pigmented lesion is extremely rare if not reported. The clinician should be aware of one such presentation of ACHL; we report a unique case of ACHL in a 30-year-old female with such a pigmented lesion in close contact with amalgam restorations. The lesion regressed considerably in a year after replacement of the restoration with posterior composites.
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spelling pubmed-42123992014-10-31 Amalgam Contact Hypersensitivity Lesion: An Unusual Presentation-Report Of A Rare Case Ramnarayan, BK Maligi, PM Smitha, T Patil, US Ann Med Health Sci Res Case Report Amalgam or its components may cause Type IV hypersensitivity reactions on the oral mucosa. These amalgam contact hypersensitivity lesions (ACHL) present as white striae and plaques, erythematous, erosive, atrophic, or ulcerative lesions. Postinflammatory pigmentation in such lesions and pigmentation due to amalgam incorporation in the soft tissue have been reported in the literature. However, ACHL presenting primarily as a black pigmented lesion is extremely rare if not reported. The clinician should be aware of one such presentation of ACHL; we report a unique case of ACHL in a 30-year-old female with such a pigmented lesion in close contact with amalgam restorations. The lesion regressed considerably in a year after replacement of the restoration with posterior composites. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4212399/ /pubmed/25364611 http://dx.doi.org/10.4103/2141-9248.141981 Text en Copyright: © Annals of Medical and Health Sciences Research 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
Ramnarayan, BK
Maligi, PM
Smitha, T
Patil, US
Amalgam Contact Hypersensitivity Lesion: An Unusual Presentation-Report Of A Rare Case
title Amalgam Contact Hypersensitivity Lesion: An Unusual Presentation-Report Of A Rare Case
title_full Amalgam Contact Hypersensitivity Lesion: An Unusual Presentation-Report Of A Rare Case
title_fullStr Amalgam Contact Hypersensitivity Lesion: An Unusual Presentation-Report Of A Rare Case
title_full_unstemmed Amalgam Contact Hypersensitivity Lesion: An Unusual Presentation-Report Of A Rare Case
title_short Amalgam Contact Hypersensitivity Lesion: An Unusual Presentation-Report Of A Rare Case
title_sort amalgam contact hypersensitivity lesion: an unusual presentation-report of a rare case
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4212399/
https://www.ncbi.nlm.nih.gov/pubmed/25364611
http://dx.doi.org/10.4103/2141-9248.141981
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