Year 2022 / Volume 114 / Number 3
Letter
Small bowel angioedema. An unusual condition with an interesting differential diagnosis

178-179

DOI: 10.17235/reed.2021.8407/2021

Francisco J. González Sánchez, María José Galante, Carmen González-Carreró Sixto, Javier García Poza, Sara Sánchez Bernal, Beatriz Castro Senosain, Inés García,

Abstract
We present the case of a 35-year-old woman with a prior history of hereditary angioedema (HA) who was admitted to the emergency department with epigastric pain, vomiting and sweating. Laboratory tests showed raised APR levels (CRP and leukocytosis).
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References
1.- Romeu Vilar D. López Rey J. (2015) Angioedema de intestino delgado secundario a inhibidor de la enzima convertidora de la angiotensina Radiología 57, 5, 449-450
2.- De la Cruz RA, Oliver JM , Bueno A et als ( 2002) Angioedema hereditario: una causa infrecuente de abdomen agudo. Hallazgos en la TC y ecografía abdominal Radiología 44, 3 122-124
3.- Poza Cordón J, de María Pallarés P, Caballero Molina T. Ultrasound findings in an abdominal crisis of a patient with hereditary angioedema. Rev Esp Enferm Dig. 2020 May;112(5):418
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Citation tools
González Sánchez F, Galante M, González-Carreró Sixto C, García Poza J, Sánchez Bernal S, Castro Senosain B, et all. Small bowel angioedema. An unusual condition with an interesting differential diagnosis. 8407/2021


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Publication history

Received: 18/10/2021

Accepted: 19/10/2021

Online First: 16/11/2021

Published: 07/03/2022

Article Online First time: 29 days

Article editing time: 140 days


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