Literature DB >> 24141983

Gastrointestinal manifestations, diagnosis, and management of hereditary angioedema.

Sujai Jalaj1, James S Scolapio.   

Abstract

Abdominal pain is one of the most common conditions in clinical practice and yet a challenging complaint to accurately diagnose due to the vast number of possible etiologies. When other health care providers cannot identify the cause of abdominal pain, gastroenterologists are often looked upon to help solve the diagnostic dilemma. Consequently, it is incumbent upon gastroenterologists to be well versed in the diagnosis and management of not only common but also rare causes of abdominal pain. One such uncommon but well-described cause of abdominal pain is angioedema of the intestinal tract due to hereditary angioedema. Acute onset, recurrent abdominal pain of varying severity is its most common presenting symptom, and misdiagnosis can not only lead to unnecessary surgical procedures but also death. The purpose of this review is to raise awareness among gastroenterologists about hereditary angioedema as a potential cause of recurrent, unexplained abdominal pain.

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Year:  2013        PMID: 24141983     DOI: 10.1097/MCG.0b013e31829e7edf

Source DB:  PubMed          Journal:  J Clin Gastroenterol        ISSN: 0192-0790            Impact factor:   3.062


  10 in total

1.  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

2.  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

Review 3.  Diagnosis and screening of patients with hereditary angioedema in primary care.

Authors:  Maria Paula Henao; Jennifer L Kraschnewski; Theodore Kelbel; Timothy J Craig
Journal:  Ther Clin Risk Manag       Date:  2016-05-02       Impact factor: 2.423

Review 4.  Angioedema in the emergency department: a practical guide to differential diagnosis and management.

Authors:  Jonathan A Bernstein; Paolo Cremonesi; Thomas K Hoffmann; John Hollingsworth
Journal:  Int J Emerg Med       Date:  2017-04-13

5.  Hereditary Angioedema Type II: First Presentation in Adulthood with Recurrent Severe Abdominal Pain.

Authors:  Mohamed Abuzakouk; Nada AlMahmeed; Esat Memisoglu; Martine McManus; Aydamir Alrakawi
Journal:  Case Reports Immunol       Date:  2018-10-29

6.  Colonic Intussusception Secondary to Hereditary Angioedema.

Authors:  Justin Roy; Rama Vunnam; Venkata Subhash Gorrepati; Deborah Bethards; Thomas McGarrity
Journal:  ACG Case Rep J       Date:  2021-01-13

7.  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

8.  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

9.  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

Review 10.  The Genetics of Hereditary Angioedema: A Review.

Authors:  Rosa Santacroce; Giovanna D'Andrea; Angela Bruna Maffione; Maurizio Margaglione; Maria d'Apolito
Journal:  J Clin Med       Date:  2021-05-09       Impact factor: 4.241

  10 in total

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