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Abdominal hereditary angio-oedema caught on magnetic resonance imaging

A 17-year-old woman presented with a 3-year history of recurrent, severe abdominal pain with spontaneous resolution within a few days. An ultrasound revealed nothing more than free fluid within the pelvis. An MRI of the small bowel was done within 24 hours of abdominal pain onset, which revealed ext...

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Autores principales: Siow, Mayven Tien Li, Robertson, Alexander Myles, Ghurye, Rohit R, Blaker, Paul A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8720948/
https://www.ncbi.nlm.nih.gov/pubmed/34972776
http://dx.doi.org/10.1136/bcr-2021-246339
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author Siow, Mayven Tien Li
Robertson, Alexander Myles
Ghurye, Rohit R
Blaker, Paul A
author_facet Siow, Mayven Tien Li
Robertson, Alexander Myles
Ghurye, Rohit R
Blaker, Paul A
author_sort Siow, Mayven Tien Li
collection PubMed
description A 17-year-old woman presented with a 3-year history of recurrent, severe abdominal pain with spontaneous resolution within a few days. An ultrasound revealed nothing more than free fluid within the pelvis. An MRI of the small bowel was done within 24 hours of abdominal pain onset, which revealed extensive submucosal oedema associated with moderate volume ascites. A repeat MRI of the small bowel after 72 hours showed near-complete resolution of these changes. Checking C1 inhibitor levels confirmed a diagnosis of hereditary angio-oedema with an abdominal presentation. This is a rare cause of recurrent abdominal pain and, to our knowledge, the first case in which MR images have been obtained during and after an acute attack.
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spelling pubmed-87209482022-01-14 Abdominal hereditary angio-oedema caught on magnetic resonance imaging Siow, Mayven Tien Li Robertson, Alexander Myles Ghurye, Rohit R Blaker, Paul A BMJ Case Rep Case Report A 17-year-old woman presented with a 3-year history of recurrent, severe abdominal pain with spontaneous resolution within a few days. An ultrasound revealed nothing more than free fluid within the pelvis. An MRI of the small bowel was done within 24 hours of abdominal pain onset, which revealed extensive submucosal oedema associated with moderate volume ascites. A repeat MRI of the small bowel after 72 hours showed near-complete resolution of these changes. Checking C1 inhibitor levels confirmed a diagnosis of hereditary angio-oedema with an abdominal presentation. This is a rare cause of recurrent abdominal pain and, to our knowledge, the first case in which MR images have been obtained during and after an acute attack. BMJ Publishing Group 2021-12-31 /pmc/articles/PMC8720948/ /pubmed/34972776 http://dx.doi.org/10.1136/bcr-2021-246339 Text en © BMJ Publishing Group Limited 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Case Report
Siow, Mayven Tien Li
Robertson, Alexander Myles
Ghurye, Rohit R
Blaker, Paul A
Abdominal hereditary angio-oedema caught on magnetic resonance imaging
title Abdominal hereditary angio-oedema caught on magnetic resonance imaging
title_full Abdominal hereditary angio-oedema caught on magnetic resonance imaging
title_fullStr Abdominal hereditary angio-oedema caught on magnetic resonance imaging
title_full_unstemmed Abdominal hereditary angio-oedema caught on magnetic resonance imaging
title_short Abdominal hereditary angio-oedema caught on magnetic resonance imaging
title_sort abdominal hereditary angio-oedema caught on magnetic resonance imaging
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8720948/
https://www.ncbi.nlm.nih.gov/pubmed/34972776
http://dx.doi.org/10.1136/bcr-2021-246339
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