Literature DB >> 20888081

[Acute pancreatitis associated with hereditary angioedema].

David Marín García1, Angel Ceballos Torres, Antonio Ruiz Serrato, Miguel Ángel García Ordóñez.   

Abstract

Hereditary angioedema (HAE) is an infrequent, recurrent, and potentially lethal disorder caused by a deficiency of C(1) inhibitor or its activity. Abdominal pain secondary to bowel edema is common in these patients. However, a thorough literature search yielded only six previously reported cases of pancreatitis associated with this entity. 2010 Elsevier España, S.L. All rights reserved.

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Year:  2010        PMID： 20888081     DOI： 10.1016/j.gastrohep.2010.07.005

Source DB:  PubMed          Journal:  Gastroenterol Hepatol        ISSN： 0210-5705            Impact factor:   2.102


  4 in total

Review 1.  Brazilian guidelines for the diagnosis and treatment of hereditary angioedema.

Authors:  Pedro Giavina-Bianchi; Alfeu T França; Anete S Grumach; Abílio A Motta; Fátima R Fernandes; Regis A Campos; Solange O Valle; Nelson A Rosário; Dirceu Sole
Journal:  Clinics (Sao Paulo)       Date:  2011       Impact factor: 2.365

2.  Hereditary Angioedema and Gastrointestinal Complications: An Extensive Review of the Literature.

Authors:  Napoleon Patel; Lisbet D Suarez; Sakshi Kapur; Leonard Bielory
Journal:  Case Reports Immunol       Date:  2015-08-03

3.  Yellow urticaria and biliary pancreatitis.

Authors:  Eira Mabel Nava Cruz; Juan Pablo Castanedo-Cázares; Diana Vianney Hernández Blanco; Bertha Torres-Álvarez
Journal:  JAAD Case Rep       Date:  2017-09-08

4.  Hereditary Angioedema-Associated Acute Pancreatitis in C1-Inhibitor Deficient and Normal C1-Inhibitor Patients: Case Reports and Literature Review.

Authors:  Camila Lopes Veronez; Régis Albuquerque Campos; Rosemeire Navickas Constantino-Silva; Priscila Nicolicht; João Bosco Pesquero; Anete Sevciovic Grumach
Journal:  Front Med (Lausanne)       Date:  2019-04-17
  4 in total

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