Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Cargini, Pasqualino, Civica, Maria, Sollima, Laura, Di Cola, Emanuela, Pontecorvi, Emanuele, Cutilli, Tommaso
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
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
_version_ 1782318188749389824
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
work_keys_str_mv AT carginipasqualino orallymphomatoidgranulomatosisthefirstsignofararediseaseacasereport
AT civicamaria orallymphomatoidgranulomatosisthefirstsignofararediseaseacasereport
AT sollimalaura orallymphomatoidgranulomatosisthefirstsignofararediseaseacasereport
AT dicolaemanuela orallymphomatoidgranulomatosisthefirstsignofararediseaseacasereport
AT pontecorviemanuele orallymphomatoidgranulomatosisthefirstsignofararediseaseacasereport
AT cutillitommaso orallymphomatoidgranulomatosisthefirstsignofararediseaseacasereport