Year 2020 / Volume 112 / Number 5
Letter
Ultrasound findings in an abdominal crisis of a patient with hereditary angioedema

418

DOI: 10.17235/reed.2020.6469/2019

Joaquín Poza Cordón, Pedro de María Pallarés, Teresa Caballero Molina,

Abstract
ereditary Angioedema (HAE) is a rare autosomal-dominant disease caused by serum C1 inhibitor deficiency. This deficiency leads to an up-regulation of complement, activating the bradykinin pathway and causing vascular permeability and subsequent mucosal edema. Abdominal angioedema is a less recognized type of angioedema and the clinical signs may range from subtle, diffuse abdominal pain and nausea, to overt peritonitis. We describe one case of abdominal angioedema in a patient with known HAE that were diagnosed by ultrasound.
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References
1. Caballero Molina T., Pedrosa Delgado M., Gómez Traseira C. Angioedema hereditario. Med Clin (Barc) 2015;145(8):356–65. Doi: 10.1016/j.medcli.2014.12.012.
2. Cicardi M., Aberer W., Banerji A., Bas M., Bernstein JA., Bork K., et al. Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working Group. Allergy 2014;69(5):602–16. Doi: 10.1111/all.12380.
3. Riguzzi C., Losonczy L., Teismann N., Herring AA., Nagdev A. Gastrointestinal Manifestations of Hereditary Angioedema Diagnosed by Ultrasound in the Emergency Department. West J Emerg Med 2014;15(7):816. Doi: 10.5811/WESTJEM.2014.7.21636.
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Poza Cordón J, de María Pallarés P, Caballero Molina T. Ultrasound findings in an abdominal crisis of a patient with hereditary angioedema . 6469/2019


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Publication history

Received: 29/06/2019

Accepted: 09/07/2019

Online First: 27/04/2020

Published: 08/05/2020

Article Online First time: 303 days

Article editing time: 314 days


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