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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...

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Autores principales: Ciacci, Carolina, Bucci, Cristina, Zingone, Fabiana, Iovino, Paola, Amato, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
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.
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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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