Literature DB >> 33685557

Recurrent and acute abdominal pain as the main clinical manifestation in patients with hereditary angioedema.

Yang Cao1, Shuang Liu1, Yuxiang Zhi1.   

Abstract

Background: Hereditary angioedema (HAE) is a rare disease that often leads to misdiagnosis. The delay of diagnosis is > 10 years in China. Recurrent and acute abdominal pain is one of the common symptoms of HAE. Because of the high misdiagnosis rate, it usually results in unnecessary surgical procedures. This study focused on the clinical symptoms and management of HAE-related abdominal attacks in Chinese patients to provide some new insight for the emergency department (ED) physicians and gastroenterologists.
Methods: A Web-based survey was conducted among 107 patients with HAE from 94 unrelated families. Detailed questions with respect to the abdominal attacks were asked, including the frequency, symptoms, and duration before and after confirmed diagnosis. The demographic characteristics, diagnosis process, and treatment outcomes were also included.
Results: Approximately 70% of the patients with HAE presented with abdominal symptoms during the onset of edema, mostly characterized by pain (94.8%), nausea (83.1%), vomiting (83.1%), diarrhea (59.7%), and constipation (23.4%). The patients were easily misdiagnosed as having gastroenteritis (35.1%) and appendicitis (10.4%), and 24.7% of them received unnecessary appendectomy or laparotomy. Danazol, a widely used drug for long-term prophylaxis of HAE in China, can reduce the attack frequency and alleviate the abdominal symptoms, but the adverse effects are also significant and more severe in women. Conclusions: Abdominal symptoms are common and important clinical features of HAE but are easily confused with other gastrointestinal diseases. ED physicians and gastroenterologists should consider HAE when patients experience recurrent and unexplained abdominal pain. Proper medical treatment should be administered in a timely manner if an HAE diagnosis is confirmed and efforts are required to increase access in China to medications both for on-demand treatment and long-term prophylaxis.

Entities:  

Year:  2021        PMID: 33685557      PMCID: PMC8133019          DOI: 10.2500/aap.2021.42.210001

Source DB:  PubMed          Journal:  Allergy Asthma Proc        ISSN: 1088-5412            Impact factor:   2.587


  19 in total

1.  The international WAO/EAACI guideline for the management of hereditary angioedema-The 2017 revision and update.

Authors:  M Maurer; M Magerl; I Ansotegui; E Aygören-Pürsün; S Betschel; K Bork; T Bowen; H Balle Boysen; H Farkas; A S Grumach; M Hide; C Katelaris; R Lockey; H Longhurst; W R Lumry; I Martinez-Saguer; D Moldovan; A Nast; R Pawankar; P Potter; M Riedl; B Ritchie; L Rosenwasser; M Sánchez-Borges; Y Zhi; B Zuraw; T Craig
Journal:  Allergy       Date:  2018-03-12       Impact factor: 13.146

Review 2.  Clinical practice. Hereditary angioedema.

Authors:  Bruce L Zuraw
Journal:  N Engl J Med       Date:  2008-09-04       Impact factor: 91.245

3.  Clinical features of hereditary angioedema in Chinese patients: new findings and differences from other populations.

Authors:  Ying-Yang Xu; Ying Jiang; Yu-Xiang Zhi; Jia Yin; Liang-Lu Wang; Li-Ping Wen; Jian-Qing Gu; Kai Guan; Hong-Yu Zhang
Journal:  Eur J Dermatol       Date:  2013 Jul-Aug       Impact factor: 3.328

Review 4.  The role of the complement system in hereditary angioedema.

Authors:  Dorottya Csuka; Nóra Veszeli; Lilian Varga; Zoltán Prohászka; Henriette Farkas
Journal:  Mol Immunol       Date:  2017-06-07       Impact factor: 4.407

Review 5.  Current update on cellular and molecular mechanisms of hereditary angioedema.

Authors:  Hannah H Walford; Bruce L Zuraw
Journal:  Ann Allergy Asthma Immunol       Date:  2014-01-29       Impact factor: 6.347

6.  Colorectal intussusception: an unusual gastrointestinal complication of hereditary angioedema.

Authors:  A Witschi; L Krähenbühl; E Frei; J Saltzman; P J Späth; U R Müller
Journal:  Int Arch Allergy Immunol       Date:  1996-09       Impact factor: 2.749

7.  A UK national audit of hereditary and acquired angioedema.

Authors:  S Jolles; P Williams; E Carne; H Mian; A Huissoon; G Wong; S Hackett; J Lortan; V Platts; H Longhurst; S Grigoriadou; J Dempster; S Deacock; S Khan; J Darroch; C Simon; M Thomas; V Pavaladurai; H Alachkar; A Herwadkar; M Abinun; P Arkwright; M Tarzi; M Helbert; C Bangs; C Pastacaldi; C Phillips; H Bennett; T El-Shanawany
Journal:  Clin Exp Immunol       Date:  2014-01       Impact factor: 4.330

8.  Frequent de novo mutations and exon deletions in the C1inhibitor gene of patients with angioedema.

Authors:  E Pappalardo; M Cicardi; C Duponchel; A Carugati; S Choquet; A Agostoni; M Tosi
Journal:  J Allergy Clin Immunol       Date:  2000-12       Impact factor: 10.793

9.  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

10.  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
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  5 in total

1.  Hereditary angioedema again revisited.

Authors:  Joseph A Bellanti; Russell A Settipane
Journal:  Allergy Asthma Proc       Date:  2021-03-01       Impact factor: 2.587

2.  Evaluation and management of adverse reactions to the COVID-2019 vaccines.

Authors:  Joseph A Bellanti; Russell A Settipane
Journal:  Allergy Asthma Proc       Date:  2022-01-01       Impact factor: 2.587

3.  Long-COVID and loss of smell: A post-COVID olfactory dysfunction that continues to challenge the allergist/immunologist.

Authors:  Joseph A Bellanti; Russell A Settipane
Journal:  Allergy Asthma Proc       Date:  2022-03-01       Impact factor: 2.587

4.  Validation of diagnostic and predictive biomarkers for hereditary angioedema via plasma N-glycomics.

Authors:  Zejian Zhang; Xue Wang; Jianqing Gu; Jianqiang Wu; Yang Cao; Yingyang Xu; Lisha Li; Kai Guan; Peng Liu; Jia Yin; Yuxiang Zhi; Shuyang Zhang
Journal:  Clin Transl Allergy       Date:  2021-12       Impact factor: 5.871

Review 5.  Hereditary Angioedema: Diagnostic Algorithm and Current Treatment Concepts.

Authors:  Ankur Kumar Jindal; Anuradha Bishnoi; Sunil Dogra
Journal:  Indian Dermatol Online J       Date:  2021-11-22
  5 in total

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