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A fatal case of rapid gingival enlargement: Case report with brief review
Myeloid sarcoma (MS) is a rare extramedullary tumor composed of primitive granulocytic cells. These lesions are commonly associated with other hematologic disorders such as myeloid leukemia and other myeloproliferative neoplasms. Although extremely rare in the oral cavity, this lesion was reported i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065429/ https://www.ncbi.nlm.nih.gov/pubmed/24959052 http://dx.doi.org/10.4103/0973-029X.131938 |
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author | Ponnam, Srinivas Rao Srivastava, Gautam Jampani, Narendradev Kamath, V. V. |
author_facet | Ponnam, Srinivas Rao Srivastava, Gautam Jampani, Narendradev Kamath, V. V. |
author_sort | Ponnam, Srinivas Rao |
collection | PubMed |
description | Myeloid sarcoma (MS) is a rare extramedullary tumor composed of primitive granulocytic cells. These lesions are commonly associated with other hematologic disorders such as myeloid leukemia and other myeloproliferative neoplasms. Although extremely rare in the oral cavity, this lesion was reported in gingiva, palate, buccal mucosa and extraction sockets. MS is an aggressive lesion associated with poor prognosis. Early identification and prompt treatment holds the key for increasing the disease-free period in these patients. In this context, we report a rare and aggressive case of MS, which ran a fatal course in a 45-year-old female patient. |
format | Online Article Text |
id | pubmed-4065429 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-40654292014-06-23 A fatal case of rapid gingival enlargement: Case report with brief review Ponnam, Srinivas Rao Srivastava, Gautam Jampani, Narendradev Kamath, V. V. J Oral Maxillofac Pathol Case Report Myeloid sarcoma (MS) is a rare extramedullary tumor composed of primitive granulocytic cells. These lesions are commonly associated with other hematologic disorders such as myeloid leukemia and other myeloproliferative neoplasms. Although extremely rare in the oral cavity, this lesion was reported in gingiva, palate, buccal mucosa and extraction sockets. MS is an aggressive lesion associated with poor prognosis. Early identification and prompt treatment holds the key for increasing the disease-free period in these patients. In this context, we report a rare and aggressive case of MS, which ran a fatal course in a 45-year-old female patient. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4065429/ /pubmed/24959052 http://dx.doi.org/10.4103/0973-029X.131938 Text en Copyright: © Journal of Oral and Maxillofacial Pathology 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 Ponnam, Srinivas Rao Srivastava, Gautam Jampani, Narendradev Kamath, V. V. A fatal case of rapid gingival enlargement: Case report with brief review |
title | A fatal case of rapid gingival enlargement: Case report with brief review |
title_full | A fatal case of rapid gingival enlargement: Case report with brief review |
title_fullStr | A fatal case of rapid gingival enlargement: Case report with brief review |
title_full_unstemmed | A fatal case of rapid gingival enlargement: Case report with brief review |
title_short | A fatal case of rapid gingival enlargement: Case report with brief review |
title_sort | fatal case of rapid gingival enlargement: case report with brief review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065429/ https://www.ncbi.nlm.nih.gov/pubmed/24959052 http://dx.doi.org/10.4103/0973-029X.131938 |
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