Literature DB >> 20954277

Diagnosis and management of angioedema with abdominal involvement: a gastroenterology perspective.

Ugochukwu C Nzeako1.   

Abstract

Abdominal involvement in angioedema is often a challenge to diagnose. Acute onset abdominal pain is its most common presenting symptom, and misdiagnosis may lead to unnecessary surgical intervention. Familiarity with the types and presentations of angioedema can be invaluable to clinicians as they consider the differential diagnoses of a patient presenting with abdominal pain. Detailed personal and family histories, careful physical examination of the patient, combined with knowledge of angioedema types, can help clinicians perform their diagnostic evaluation. An accurate diagnosis is essential in order to provide appropriate treatment to patients with angioedema. Depending upon the diagnosis, treatment may be the avoidance of provoking factors (such as allergens or medications), inhibiting histamine-provoked reactions, or treating C1 esterase inhibitor deficiency.

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Year:  2010        PMID: 20954277      PMCID: PMC2957599          DOI: 10.3748/wjg.v16.i39.4913

Source DB:  PubMed          Journal:  World J Gastroenterol        ISSN: 1007-9327            Impact factor:   5.742


  35 in total

Review 1.  Acquired deficiency of the inhibitor of the first complement component: presentation, diagnosis, course, and conventional management.

Authors:  Lorenza Chiara Zingale; Roberto Castelli; Andrea Zanichelli; Marco Cicardi
Journal:  Immunol Allergy Clin North Am       Date:  2006-11       Impact factor: 3.479

2.  Investigation of angioedema associated with the use of angiotensin-converting enzyme inhibitors and angiotensin receptor blockers.

Authors:  Baiju Malde; Jane Regalado; Paul A Greenberger
Journal:  Ann Allergy Asthma Immunol       Date:  2007-01       Impact factor: 6.347

3.  Hereditary angiodema: a current state-of-the-art review, IV: short- and long-term treatment of hereditary angioedema: out with the old and in with the new?

Authors:  Bruce L Zuraw
Journal:  Ann Allergy Asthma Immunol       Date:  2008-01       Impact factor: 6.347

4.  Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III.

Authors:  Sven Cichon; Ludovic Martin; Hans Christian Hennies; Felicitas Müller; Karen Van Driessche; Anna Karpushova; Wim Stevens; Roberto Colombo; Thomas Renné; Christian Drouet; Konrad Bork; Markus M Nöthen
Journal:  Am J Hum Genet       Date:  2006-10-18       Impact factor: 11.025

Review 5.  Idiopathic recurrent angioedema.

Authors:  Evangelo Frigas; Miguel Park
Journal:  Immunol Allergy Clin North Am       Date:  2006-11       Impact factor: 3.479

Review 6.  Fresh frozen plasma for the treatment of hereditary angioedema.

Authors:  Michael Prematta; Joshua G Gibbs; Ellen L Pratt; Tracy R Stoughton; Timothy J Craig
Journal:  Ann Allergy Asthma Immunol       Date:  2007-04       Impact factor: 6.347

7.  Hereditary angioedema with normal C1 inhibitor: clinical symptoms and course.

Authors:  Konrad Bork; Döndü Gül; Jochen Hardt; Georg Dewald
Journal:  Am J Med       Date:  2007-11       Impact factor: 4.965

8.  Benazepril induced isolated visceral angioedema: a rare and under diagnosed adverse effect of angiotensin converting enzyme inhibitors.

Authors:  Mutahir U Khan; Muhammad A Baig; Rana A Javed; Shaukat Ali; Umair R Qamar; Balendu C Vasavada; Ijaz A Khan
Journal:  Int J Cardiol       Date:  2007-03-29       Impact factor: 4.164

9.  Symptoms, course, and complications of abdominal attacks in hereditary angioedema due to C1 inhibitor deficiency.

Authors:  Konrad Bork; Petra Staubach; Alexander J Eckardt; Jochen Hardt
Journal:  Am J Gastroenterol       Date:  2006-02-08       Impact factor: 10.864

Review 10.  Hereditary angiodema: a current state-of-the-art review, VII: Canadian Hungarian 2007 International Consensus Algorithm for the Diagnosis, Therapy, and Management of Hereditary Angioedema.

Authors:  Tom Bowen; Marco Cicardi; Konrad Bork; Bruce Zuraw; Mike Frank; Bruce Ritchie; Henriette Farkas; Lilian Varga; Lorenza C Zingale; Karen Binkley; Eric Wagner; Peggy Adomaitis; Kristylea Brosz; Jeanne Burnham; Richard Warrington; Chrystyna Kalicinsky; Sean Mace; Christine McCusker; Robert Schellenberg; Lucia Celeste; Jacques Hebert; Karen Valentine; Man-Chiu Poon; Bazir Serushago; Doris Neurath; William Yang; Gina Lacuesta; Andrew Issekutz; Azza Hamed; Palinder Kamra; John Dean; Amin Kanani; Donald Stark; Georges-Etienne Rivard; Eric Leith; Ellie Tsai; Susan Waserman; Paul K Keith; David Page; Silvia Marchesin; Hilary J Longhurst; Wolfhart Kreuz; Eva Rusicke; Inmaculada Martinez-Saguer; Emel Aygören-Pürsün; George Harmat; George Füst; Henry Li; Laurence Bouillet; Teresa Caballero; Dumitru Moldovan; Peter J Späth; Sara Smith-Foltz; Istvan Nagy; Erik W Nielsen; Christoph Bucher; Patrik Nordenfelt; Zhi Yu Xiang
Journal:  Ann Allergy Asthma Immunol       Date:  2008-01       Impact factor: 6.347

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  11 in total

1.  A case report looking at ACE inhibitors as the cause of angioedema during dental treatment.

Authors:  P Raval
Journal:  Br Dent J       Date:  2014-01       Impact factor: 1.626

2.  Intestinal angioedema caused by an acquired C1 esterase inhibitor deficiency associated with underlying splenic marginal zone lymphoma.

Authors:  Thanita Thongtan; Anasua Deb; Genanew Bedanie; Mohamed Elmassry; Matthew Soape; Kenneth Nugent
Journal:  Proc (Bayl Univ Med Cent)       Date:  2021-02-22

3.  Isolated angioedema of the bowel caused by aspirin.

Authors:  Karim Osman; Ayse Tuba Kendi; Daniel Maselli
Journal:  Clin J Gastroenterol       Date:  2021-05-17

Review 4.  Hereditary angioedema: what the gastroenterologist needs to know.

Authors:  M Aamir Ali; Marie L Borum
Journal:  Clin Exp Gastroenterol       Date:  2014-11-20

5.  Abdominal attacks and treatment in hereditary angioedema with C1-inhibitor deficiency.

Authors:  Eitan Rubinstein; Leslie E Stolz; Albert L Sheffer; Chris Stevens; Athos Bousvaros
Journal:  BMC Gastroenterol       Date:  2014-04-09       Impact factor: 3.067

6.  Hereditary angioedema with C1 inhibitor (C1-INH) deficit: the strength of recognition (51 cases).

Authors:  N T M L Fragnan; A L N Tolentino; G B Borba; A C Oliveira; J A Simões; S M U Palma; R N Constantino-Silva; A S Grumach
Journal:  Braz J Med Biol Res       Date:  2018-11-14       Impact factor: 2.590

7.  Quantification of human C1 esterase inhibitor protein using an automated turbidimetric immunoassay.

Authors:  Clare E Tange; Amrit Kaur; Nisha Verma; Alaco Hickey; Sofia Grigoriadou; Chris Scott; Sorena Kiani; Rachael Steven; Mark Ponsford; Tariq El-Shanawany; Stephen Jolles; Stephen Harding; Antony R Parker
Journal:  J Clin Lab Anal       Date:  2018-07-29       Impact factor: 2.352

8.  Significant predictive factors of the severity and outcomes of the first attack of acute angioedema in children.

Authors:  Yuan-Jhen Syue; Chao-Jui Li; Wen-Liang Chen; Tsung-Han Lee; Cheng-Chieh Huang; Mei-Chueh Yang; Chih-Ming Lin; Meng-Huan Wu; Chu-Chung Chou; Chin-Fu Chang; Yan-Ren Lin
Journal:  BMC Pediatr       Date:  2019-11-11       Impact factor: 2.125

9.  Abdominal and pelvic imaging in the diagnosis of acute abdominal attacks in patients with hereditary angioedema due to C1-inhibitor deficiency.

Authors:  Piotr Obtułowicz; Marcin Stobiecki; Wojciech Dyga; Aldona Juchacz; Tadeusz Popiela; Krystyna Obtułowicz
Journal:  Postepy Dermatol Alergol       Date:  2021-08-13       Impact factor: 1.664

10.  Isolated Intestinal Angioedema Secondary to a Food Allergen.

Authors:  Ammar Hassan; Simcha Weissman; Michael A Sciarra; John Sotiriadis
Journal:  ACG Case Rep J       Date:  2019-09-12
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