Literature DB >> 32732812

Gastrointestinal manifestations of angioedema: a potential area of misdiagnosis.

Ilaria Mormile1, Antonio Cocchiaro2, Maria Bova1, Stefania Loffredo1,3, Amato de Paulis1, Giuseppe Spadaro1, Angelica Petraroli1.   

Abstract

Abdominal pain is one of the most common conditions leading people to the emergency department. An uncommon but well described cause of abdominal pain is angioedema of the gastrointestinal tract due to recurrent angioedema without wheals. Abdominal involvement is very common in hereditary angioedema (HAE), but it is also described in acquired angioedema and allergic forms. In patients with HAE, the involvement of gastrointestinal tract with resultant abdominal pain occurs in 43-93% of cases. Attacks can involve the entire gastrointestinal tract, such as the oropharynx, small intestine, colon, liver, or pancreas. Pain is the most common gastrointestinal symptom, and it may occur for many years even without cutaneous or respiratory symptoms. The case report we included in this article emphasizes the importance of accurate evaluation of personal and family history in patients with a long history of acute, severe, and unexplained abdominal pain, and it gives an example of how diagnostic delay may be longer if gastroenterological symptoms are the predominant clinical presentation. Furthermore, sometimes the simultaneous presence of concomitant gastrointestinal disorders and HAE may cause difficulties in differential diagnosis. Gastroenterologists and other physicians should add HAE to their list of potential causes of unexplained abdominal pain. The initiation of appropriate prophylaxis and treatment will prevent needless suffering and useless surgical and medical procedures.
Copyright © 2020 Wolters Kluwer Health, Inc. All rights reserved.

Entities:  

Year:  2021        PMID: 32732812     DOI: 10.1097/MEG.0000000000001848

Source DB:  PubMed          Journal:  Eur J Gastroenterol Hepatol        ISSN: 0954-691X            Impact factor:   2.566


  3 in total

1.  Role of Endothelial G Protein-Coupled Receptor Kinase 2 in Angioedema.

Authors:  Jessica Gambardella; Daniela Sorriento; Maria Bova; Mariarosaria Rusciano; Stefania Loffredo; Xujun Wang; Angelica Petraroli; Laura Carucci; Ilaria Mormile; Marco Oliveti; Marco Bruno Morelli; Antonella Fiordelisi; Giuseppe Spadaro; Pietro Campiglia; Marina Sala; Bruno Trimarco; Guido Iaccarino; Gaetano Santulli; Michele Ciccarelli
Journal:  Hypertension       Date:  2020-09-08       Impact factor: 10.190

2.  The prevalence of hereditary angioedema in a Chinese cohort with decreased complement 4 levels.

Authors:  Qi Cui; Qingxiu Xu; Yaqi Yang; Wenjing Li; Nan Huang; Hao Chen; Dongxia Ma; Shuchen Zhang; Lin Yang; Rongfei Zhu
Journal:  World Allergy Organ J       Date:  2021-12-18       Impact factor: 4.084

3.  Consider Hereditary Angioedema in the Differential Diagnosis for Unexplained Recurring Abdominal Pain.

Authors:  Kyle Staller; Anthony Lembo; Aleena Banerji; Jonathan A Bernstein; Eric D Shah; Marc A Riedl
Journal:  J Clin Gastroenterol       Date:  2022-08-15       Impact factor: 3.174

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.