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Oral lymphomatoid granulomatosis, the first sign of a ‘rare disease’: a case report
INTRODUCTION: Lymphomatoid granulomatosis is an uncommon Epstein-Barr virus-positive B-cell lymphoma, an angiocentric-destructive process with a predominant T-cell background. Lymphomatoid granulomatosis is listed among rare diseases. Common localization is in the lungs. Lymphomatoid granulomatosis...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4036708/ https://www.ncbi.nlm.nih.gov/pubmed/24886196 http://dx.doi.org/10.1186/1752-1947-8-152 |
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author | Cargini, Pasqualino Civica, Maria Sollima, Laura Di Cola, Emanuela Pontecorvi, Emanuele Cutilli, Tommaso |
author_facet | Cargini, Pasqualino Civica, Maria Sollima, Laura Di Cola, Emanuela Pontecorvi, Emanuele Cutilli, Tommaso |
author_sort | Cargini, Pasqualino |
collection | PubMed |
description | INTRODUCTION: Lymphomatoid granulomatosis is an uncommon Epstein-Barr virus-positive B-cell lymphoma, an angiocentric-destructive process with a predominant T-cell background. Lymphomatoid granulomatosis is listed among rare diseases. Common localization is in the lungs. Lymphomatoid granulomatosis with oral involvement is described in only two reports. In this report, we describe a third case of oral lymphomatoid granulomatosis. CASE PRESENTATION: A 65-year-old Caucasian man with a gingival ulceration underwent a biopsy. The histological pattern was compatible with a grade III lymphomatoid granulomatosis. The staging revealed a nodular lesion in the lower lobe of his right lung. Our patient also presented with hemoptysis, an unusual and not reported clinical sign. Rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone chemotherapy was performed every three weeks for six cycles. CONCLUSIONS: The pulmonary nodule and the gingival lesion disappeared. At eight-month follow-up, our patient is disease-free. We wish to emphasize that the oral manifestation described was the first sign of the disease and allowed for diagnosis. This case report adds to the medical literature for the particular clinical presentation of this rare disease. |
format | Online Article Text |
id | pubmed-4036708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40367082014-05-29 Oral lymphomatoid granulomatosis, the first sign of a ‘rare disease’: a case report Cargini, Pasqualino Civica, Maria Sollima, Laura Di Cola, Emanuela Pontecorvi, Emanuele Cutilli, Tommaso J Med Case Rep Case Report INTRODUCTION: Lymphomatoid granulomatosis is an uncommon Epstein-Barr virus-positive B-cell lymphoma, an angiocentric-destructive process with a predominant T-cell background. Lymphomatoid granulomatosis is listed among rare diseases. Common localization is in the lungs. Lymphomatoid granulomatosis with oral involvement is described in only two reports. In this report, we describe a third case of oral lymphomatoid granulomatosis. CASE PRESENTATION: A 65-year-old Caucasian man with a gingival ulceration underwent a biopsy. The histological pattern was compatible with a grade III lymphomatoid granulomatosis. The staging revealed a nodular lesion in the lower lobe of his right lung. Our patient also presented with hemoptysis, an unusual and not reported clinical sign. Rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone chemotherapy was performed every three weeks for six cycles. CONCLUSIONS: The pulmonary nodule and the gingival lesion disappeared. At eight-month follow-up, our patient is disease-free. We wish to emphasize that the oral manifestation described was the first sign of the disease and allowed for diagnosis. This case report adds to the medical literature for the particular clinical presentation of this rare disease. BioMed Central 2014-05-15 /pmc/articles/PMC4036708/ /pubmed/24886196 http://dx.doi.org/10.1186/1752-1947-8-152 Text en Copyright © 2014 Cargini et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Cargini, Pasqualino Civica, Maria Sollima, Laura Di Cola, Emanuela Pontecorvi, Emanuele Cutilli, Tommaso Oral lymphomatoid granulomatosis, the first sign of a ‘rare disease’: a case report |
title | Oral lymphomatoid granulomatosis, the first sign of a ‘rare disease’: a case report |
title_full | Oral lymphomatoid granulomatosis, the first sign of a ‘rare disease’: a case report |
title_fullStr | Oral lymphomatoid granulomatosis, the first sign of a ‘rare disease’: a case report |
title_full_unstemmed | Oral lymphomatoid granulomatosis, the first sign of a ‘rare disease’: a case report |
title_short | Oral lymphomatoid granulomatosis, the first sign of a ‘rare disease’: a case report |
title_sort | oral lymphomatoid granulomatosis, the first sign of a ‘rare disease’: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4036708/ https://www.ncbi.nlm.nih.gov/pubmed/24886196 http://dx.doi.org/10.1186/1752-1947-8-152 |
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