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Unusual presentation of oral amyloidosis
Amyloidosis is a rare disease of difficult diagnosis that occurs due accumulation of amyloid substance localized or systemic. The oral cavity is an unusual site and can be related to both localized and systemic forms and for that reason a full investigation is necessary to determine the extent of th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632238/ https://www.ncbi.nlm.nih.gov/pubmed/26604589 http://dx.doi.org/10.4103/0976-237X.166814 |
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author | Silva, William P. P. Wastner, Bruna F. Bohn, Joslei C. Jung, Juliana E. Schussel, Juliana L. Sassi, Laurindo M. |
author_facet | Silva, William P. P. Wastner, Bruna F. Bohn, Joslei C. Jung, Juliana E. Schussel, Juliana L. Sassi, Laurindo M. |
author_sort | Silva, William P. P. |
collection | PubMed |
description | Amyloidosis is a rare disease of difficult diagnosis that occurs due accumulation of amyloid substance localized or systemic. The oral cavity is an unusual site and can be related to both localized and systemic forms and for that reason a full investigation is necessary to determine the extent of the disease. This study reports a case of a 58-year-old melanoderm male patient referred to the Department of Oral and Maxillofacial Surgery with white plaques on the tongue and multiple nodules in the region of the buccal mucosa and labial commissure, with 6 months of evolution and painful symptoms. An incisional biopsy was performed on both sites and histological examination indicated the presence of eosinophilic amorphous material within the connective tissue, positive for crystal violet staining, consistent with amyloidosis. At the present time, there is no consensus on the management of local amyloidosis. Surgical treatment of localized forms is indicated in some cases to reduce the functional prejudice. Moreover, follow-up is mandatory, both to manage recurrences and to monitor the possible evolution of the disease to the systemic form. |
format | Online Article Text |
id | pubmed-4632238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-46322382015-11-24 Unusual presentation of oral amyloidosis Silva, William P. P. Wastner, Bruna F. Bohn, Joslei C. Jung, Juliana E. Schussel, Juliana L. Sassi, Laurindo M. Contemp Clin Dent Case Report Amyloidosis is a rare disease of difficult diagnosis that occurs due accumulation of amyloid substance localized or systemic. The oral cavity is an unusual site and can be related to both localized and systemic forms and for that reason a full investigation is necessary to determine the extent of the disease. This study reports a case of a 58-year-old melanoderm male patient referred to the Department of Oral and Maxillofacial Surgery with white plaques on the tongue and multiple nodules in the region of the buccal mucosa and labial commissure, with 6 months of evolution and painful symptoms. An incisional biopsy was performed on both sites and histological examination indicated the presence of eosinophilic amorphous material within the connective tissue, positive for crystal violet staining, consistent with amyloidosis. At the present time, there is no consensus on the management of local amyloidosis. Surgical treatment of localized forms is indicated in some cases to reduce the functional prejudice. Moreover, follow-up is mandatory, both to manage recurrences and to monitor the possible evolution of the disease to the systemic form. Medknow Publications & Media Pvt Ltd 2015-09 /pmc/articles/PMC4632238/ /pubmed/26604589 http://dx.doi.org/10.4103/0976-237X.166814 Text en Copyright: © Contemporary Clinical Dentistry 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 Silva, William P. P. Wastner, Bruna F. Bohn, Joslei C. Jung, Juliana E. Schussel, Juliana L. Sassi, Laurindo M. Unusual presentation of oral amyloidosis |
title | Unusual presentation of oral amyloidosis |
title_full | Unusual presentation of oral amyloidosis |
title_fullStr | Unusual presentation of oral amyloidosis |
title_full_unstemmed | Unusual presentation of oral amyloidosis |
title_short | Unusual presentation of oral amyloidosis |
title_sort | unusual presentation of oral amyloidosis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632238/ https://www.ncbi.nlm.nih.gov/pubmed/26604589 http://dx.doi.org/10.4103/0976-237X.166814 |
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