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Buccal localization of Crohn’s disease with long-term infliximab therapy: a case report
INTRODUCTION: Cheilitis granulomatosa causes persistent idiopathic lip swelling and ulceration and it can sometimes be recognized as a unique or early manifestation of Crohn’s disease. Spontaneous remission is rare and with the lack of controlled trials, different therapeutic approaches have been us...
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/PMC4265509/ https://www.ncbi.nlm.nih.gov/pubmed/25433368 http://dx.doi.org/10.1186/1752-1947-8-397 |
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author | Ciacci, Carolina Bucci, Cristina Zingone, Fabiana Iovino, Paola Amato, Massimo |
author_facet | Ciacci, Carolina Bucci, Cristina Zingone, Fabiana Iovino, Paola Amato, Massimo |
author_sort | Ciacci, Carolina |
collection | PubMed |
description | INTRODUCTION: Cheilitis granulomatosa causes persistent idiopathic lip swelling and ulceration and it can sometimes be recognized as a unique or early manifestation of Crohn’s disease. Spontaneous remission is rare and with the lack of controlled trials, different therapeutic approaches have been used. Some cases have been treated with an exclusion diet in the attempt to rule out diet allergens, while the most popular treatments include antibiotics such as tetracycline and clofazimine tranilast, benzocaine topical or intralesional steroids, and cheiloplasty, with different outcomes. CASE PRESENTATION: We describe the case of a 23-year-old Caucasian man, primarily diagnosed with cheilitis granulomatosa for a severe lower lip swelling, and then with Crohn’s disease of the terminal ileum and anus. Treatment of Crohn’s disease with an anti-tumor necrosis factor alpha agent (infliximab) successfully induced remission of both the gastrointestinal disease and the oral lesion. CONCLUSIONS: Our recommendation is that physicians should be able to recognize cheilitis granulomatosa as a possible marker of a more complex systemic disease and proceed first with an accurate physical examination, and further suggest investigations of the bowel. In cases of Crohn’s disease, a therapy with biological agents can be successful. |
format | Online Article Text |
id | pubmed-4265509 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42655092014-12-15 Buccal localization of Crohn’s disease with long-term infliximab therapy: a case report Ciacci, Carolina Bucci, Cristina Zingone, Fabiana Iovino, Paola Amato, Massimo J Med Case Rep Case Report INTRODUCTION: Cheilitis granulomatosa causes persistent idiopathic lip swelling and ulceration and it can sometimes be recognized as a unique or early manifestation of Crohn’s disease. Spontaneous remission is rare and with the lack of controlled trials, different therapeutic approaches have been used. Some cases have been treated with an exclusion diet in the attempt to rule out diet allergens, while the most popular treatments include antibiotics such as tetracycline and clofazimine tranilast, benzocaine topical or intralesional steroids, and cheiloplasty, with different outcomes. CASE PRESENTATION: We describe the case of a 23-year-old Caucasian man, primarily diagnosed with cheilitis granulomatosa for a severe lower lip swelling, and then with Crohn’s disease of the terminal ileum and anus. Treatment of Crohn’s disease with an anti-tumor necrosis factor alpha agent (infliximab) successfully induced remission of both the gastrointestinal disease and the oral lesion. CONCLUSIONS: Our recommendation is that physicians should be able to recognize cheilitis granulomatosa as a possible marker of a more complex systemic disease and proceed first with an accurate physical examination, and further suggest investigations of the bowel. In cases of Crohn’s disease, a therapy with biological agents can be successful. BioMed Central 2014-11-30 /pmc/articles/PMC4265509/ /pubmed/25433368 http://dx.doi.org/10.1186/1752-1947-8-397 Text en © Ciacci et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), 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 Ciacci, Carolina Bucci, Cristina Zingone, Fabiana Iovino, Paola Amato, Massimo Buccal localization of Crohn’s disease with long-term infliximab therapy: a case report |
title | Buccal localization of Crohn’s disease with long-term infliximab therapy: a case report |
title_full | Buccal localization of Crohn’s disease with long-term infliximab therapy: a case report |
title_fullStr | Buccal localization of Crohn’s disease with long-term infliximab therapy: a case report |
title_full_unstemmed | Buccal localization of Crohn’s disease with long-term infliximab therapy: a case report |
title_short | Buccal localization of Crohn’s disease with long-term infliximab therapy: a case report |
title_sort | buccal localization of crohn’s disease with long-term infliximab therapy: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4265509/ https://www.ncbi.nlm.nih.gov/pubmed/25433368 http://dx.doi.org/10.1186/1752-1947-8-397 |
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