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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...

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Detalles Bibliográficos
Autores principales: Roy, Justin, Vunnam, Rama, Gorrepati, Venkata Subhash, Bethards, Deborah, McGarrity, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2021
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.
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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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