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Solitary Cecal Ulcer: A Case Report

BACKGROUND: Solitary cecal ulcer is a rare disease. Its etiology is unknown and there are no pathognomonic symptoms. There are rare reports mimicking carcinoma as seen in this case. CASE PRESENTATION: A 64 year-old woman presented with a history of intermittent right lower abdominal pain for 20 year...

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Autores principales: Li, Chun Qiang, He, An-Qi, Liu, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9010653/
https://www.ncbi.nlm.nih.gov/pubmed/35433810
http://dx.doi.org/10.3389/fsurg.2022.819519
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author Li, Chun Qiang
He, An-Qi
Liu, Gang
author_facet Li, Chun Qiang
He, An-Qi
Liu, Gang
author_sort Li, Chun Qiang
collection PubMed
description BACKGROUND: Solitary cecal ulcer is a rare disease. Its etiology is unknown and there are no pathognomonic symptoms. There are rare reports mimicking carcinoma as seen in this case. CASE PRESENTATION: A 64 year-old woman presented with a history of intermittent right lower abdominal pain for 20 years and worsening for 1 year. Colonoscopy revealed an enormous cecal ulcer. The PET-CT showed increased metabolism of the lesion. She underwent a right hemicolectomy. Histopathological examination revealed chronic non-specific inflammation. A rare diagnosis of the solitary cecal ulcer was ultimately made. CONCLUSION: Solitary cecal ulcer is a rare, idiopathic entity. It mimics inflammatory bowel disease, malignancy, infection, etc. The comprehensive images of this case describe the characteristics of the disease.
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spelling pubmed-90106532022-04-16 Solitary Cecal Ulcer: A Case Report Li, Chun Qiang He, An-Qi Liu, Gang Front Surg Surgery BACKGROUND: Solitary cecal ulcer is a rare disease. Its etiology is unknown and there are no pathognomonic symptoms. There are rare reports mimicking carcinoma as seen in this case. CASE PRESENTATION: A 64 year-old woman presented with a history of intermittent right lower abdominal pain for 20 years and worsening for 1 year. Colonoscopy revealed an enormous cecal ulcer. The PET-CT showed increased metabolism of the lesion. She underwent a right hemicolectomy. Histopathological examination revealed chronic non-specific inflammation. A rare diagnosis of the solitary cecal ulcer was ultimately made. CONCLUSION: Solitary cecal ulcer is a rare, idiopathic entity. It mimics inflammatory bowel disease, malignancy, infection, etc. The comprehensive images of this case describe the characteristics of the disease. Frontiers Media S.A. 2022-04-01 /pmc/articles/PMC9010653/ /pubmed/35433810 http://dx.doi.org/10.3389/fsurg.2022.819519 Text en Copyright © 2022 Li, He and Liu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Surgery
Li, Chun Qiang
He, An-Qi
Liu, Gang
Solitary Cecal Ulcer: A Case Report
title Solitary Cecal Ulcer: A Case Report
title_full Solitary Cecal Ulcer: A Case Report
title_fullStr Solitary Cecal Ulcer: A Case Report
title_full_unstemmed Solitary Cecal Ulcer: A Case Report
title_short Solitary Cecal Ulcer: A Case Report
title_sort solitary cecal ulcer: a case report
topic Surgery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9010653/
https://www.ncbi.nlm.nih.gov/pubmed/35433810
http://dx.doi.org/10.3389/fsurg.2022.819519
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