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Colonic Intussusception Secondary to Hereditary Angioedema
Hereditary angioedema (HAE) is a rare genetic disease with numerous gastrointestinal manifestations. Intussusception, although rare, has been a reported complication with documentation of bowel wall edema on endoscopy during an acute flare. With the advent of synthetic C1 esterase inhibitors, this d...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7808557/ https://www.ncbi.nlm.nih.gov/pubmed/33457436 http://dx.doi.org/10.14309/crj.0000000000000498 |
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author | Roy, Justin Vunnam, Rama Gorrepati, Venkata Subhash Bethards, Deborah McGarrity, Thomas |
author_facet | Roy, Justin Vunnam, Rama Gorrepati, Venkata Subhash Bethards, Deborah McGarrity, Thomas |
author_sort | Roy, Justin |
collection | PubMed |
description | Hereditary angioedema (HAE) is a rare genetic disease with numerous gastrointestinal manifestations. Intussusception, although rare, has been a reported complication with documentation of bowel wall edema on endoscopy during an acute flare. With the advent of synthetic C1 esterase inhibitors, this disease has become more effectively treatable. This case report shows a HAE flare complicated by colonic intussusception, treated with C1 esterase inhibitor, with complete endoscopic resolution seen on hospital day 5. This case provides evidence that with proper medical treatment, an HAE flare with intussusception has the potential to resolve without any further need for surgical or endoscopic intervention. |
format | Online Article Text |
id | pubmed-7808557 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer |
record_format | MEDLINE/PubMed |
spelling | pubmed-78085572021-01-15 Colonic Intussusception Secondary to Hereditary Angioedema Roy, Justin Vunnam, Rama Gorrepati, Venkata Subhash Bethards, Deborah McGarrity, Thomas ACG Case Rep J Case Report Hereditary angioedema (HAE) is a rare genetic disease with numerous gastrointestinal manifestations. Intussusception, although rare, has been a reported complication with documentation of bowel wall edema on endoscopy during an acute flare. With the advent of synthetic C1 esterase inhibitors, this disease has become more effectively treatable. This case report shows a HAE flare complicated by colonic intussusception, treated with C1 esterase inhibitor, with complete endoscopic resolution seen on hospital day 5. This case provides evidence that with proper medical treatment, an HAE flare with intussusception has the potential to resolve without any further need for surgical or endoscopic intervention. Wolters Kluwer 2021-01-13 /pmc/articles/PMC7808557/ /pubmed/33457436 http://dx.doi.org/10.14309/crj.0000000000000498 Text en © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterology. This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Roy, Justin Vunnam, Rama Gorrepati, Venkata Subhash Bethards, Deborah McGarrity, Thomas Colonic Intussusception Secondary to Hereditary Angioedema |
title | Colonic Intussusception Secondary to Hereditary Angioedema |
title_full | Colonic Intussusception Secondary to Hereditary Angioedema |
title_fullStr | Colonic Intussusception Secondary to Hereditary Angioedema |
title_full_unstemmed | Colonic Intussusception Secondary to Hereditary Angioedema |
title_short | Colonic Intussusception Secondary to Hereditary Angioedema |
title_sort | colonic intussusception secondary to hereditary angioedema |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7808557/ https://www.ncbi.nlm.nih.gov/pubmed/33457436 http://dx.doi.org/10.14309/crj.0000000000000498 |
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