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Hematochezia due to arteriovenous malformation of the mesoappendix: a rare case report
An arteriovenous malformation (AVM) of the mesoappendix is a very rare clinical entity. The clinical features, diagnosis and management of an AVM of the mesoappendix have yet to be sufficiently explained since reports about it are scarce. We report a 57-year-old man presented with hematochezia for 2...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10097609/ https://www.ncbi.nlm.nih.gov/pubmed/37064067 http://dx.doi.org/10.1093/jscr/rjad164 |
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author | Nguyen, Tuan Anh Van Pham, Hiep Tran, Thang Manh |
author_facet | Nguyen, Tuan Anh Van Pham, Hiep Tran, Thang Manh |
author_sort | Nguyen, Tuan Anh |
collection | PubMed |
description | An arteriovenous malformation (AVM) of the mesoappendix is a very rare clinical entity. The clinical features, diagnosis and management of an AVM of the mesoappendix have yet to be sufficiently explained since reports about it are scarce. We report a 57-year-old man presented with hematochezia for 2 weeks. Upper and lower endoscopic could not find the source of bleeding. Abdominal contrast-enhanced computed tomography revealed an AVM of the mesoappendix. A laparoscopic appendectomy was performed, and he had a resolution of his symptoms. Intraoperative findings and pathological results confirmed the diagnosis of AVM of the mesoappendix. |
format | Online Article Text |
id | pubmed-10097609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-100976092023-04-14 Hematochezia due to arteriovenous malformation of the mesoappendix: a rare case report Nguyen, Tuan Anh Van Pham, Hiep Tran, Thang Manh J Surg Case Rep Case Report An arteriovenous malformation (AVM) of the mesoappendix is a very rare clinical entity. The clinical features, diagnosis and management of an AVM of the mesoappendix have yet to be sufficiently explained since reports about it are scarce. We report a 57-year-old man presented with hematochezia for 2 weeks. Upper and lower endoscopic could not find the source of bleeding. Abdominal contrast-enhanced computed tomography revealed an AVM of the mesoappendix. A laparoscopic appendectomy was performed, and he had a resolution of his symptoms. Intraoperative findings and pathological results confirmed the diagnosis of AVM of the mesoappendix. Oxford University Press 2023-04-12 /pmc/articles/PMC10097609/ /pubmed/37064067 http://dx.doi.org/10.1093/jscr/rjad164 Text en Published by Oxford University Press and JSCR Publishing Ltd. © The Author(s) 2023. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Nguyen, Tuan Anh Van Pham, Hiep Tran, Thang Manh Hematochezia due to arteriovenous malformation of the mesoappendix: a rare case report |
title | Hematochezia due to arteriovenous malformation of the mesoappendix: a rare case report |
title_full | Hematochezia due to arteriovenous malformation of the mesoappendix: a rare case report |
title_fullStr | Hematochezia due to arteriovenous malformation of the mesoappendix: a rare case report |
title_full_unstemmed | Hematochezia due to arteriovenous malformation of the mesoappendix: a rare case report |
title_short | Hematochezia due to arteriovenous malformation of the mesoappendix: a rare case report |
title_sort | hematochezia due to arteriovenous malformation of the mesoappendix: a rare case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10097609/ https://www.ncbi.nlm.nih.gov/pubmed/37064067 http://dx.doi.org/10.1093/jscr/rjad164 |
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