Literature DB >> 33554204

Acute Presentation of Undiagnosed Hereditary Angioedema of the Larynx: Averting Death.

Nikhil Rajan1, Vidhu Sharma1, Sourabha Kumar Patro2, Amit Goyal1.   

Abstract

Hereditary angioedema (HAE) differs from histamine-mediated angioedema in that it is resistant to steroids and antihistamines. Laryngeal attacks of this condition, if not diagnosed timely, carry a mortality rate up to 34%. Rarely, this disease goes undiagnosed until late adulthood and presents a life-threatening episode that poses a management challenge to the emergency physician. We report the case of a 48-year-old man who presented to the emergency department with progressive breathing difficulty two hours after consuming a carbonated drink. Clinical examination revealed supraglottic edema. He did not respond to steroids or antihistamines and required emergency tracheostomy to secure the airway due to failed intubation. Absence of symptoms such as itching or urticaria and inadequate response to steroids pointed to hereditary angioedema. Low complement factor 4 levels with low C1 esterase inhibitor functionality confirmed the diagnosis. This case report highlights the fact that delayed presentation of HAE can be life threatening and the diagnosis should be considered in all non-atopic adult patients with angioedema. © Copyright 2020 by Official Journal of the Turkish Society of Otorhinolaryngology and Head and Neck Surgery.

Entities:  

Keywords:  C1 esterase inhibitor; Hereditary angioedema; airway management; airway obstruction; tracheotomy

Year:  2020        PMID: 33554204      PMCID: PMC7846295          DOI: 10.5152/tao.2020.5994

Source DB:  PubMed          Journal:  Turk Arch Otorhinolaryngol        ISSN: 2667-7466


  11 in total

1.  A multicentre evaluation of the diagnostic efficiency of serological investigations for C1 inhibitor deficiency.

Authors:  M M Gompels; R J Lock; J E Morgan; J Osborne; A Brown; P F Virgo
Journal:  J Clin Pathol       Date:  2002-02       Impact factor: 3.411

2.  Repeated attacks of type III hereditary angioedema with factor XII mutation during pregnancy.

Authors:  S Feray; O Fain; G Kayem; N Sabourdin; I Constant; A Rigouzzo
Journal:  Int J Obstet Anesth       Date:  2018-08-02       Impact factor: 2.603

3.  Hereditary angioedema: an update on causes, manifestations and treatment.

Authors:  Hilary J Longhurst; Konrad Bork
Journal:  Br J Hosp Med (Lond)       Date:  2019-07-02       Impact factor: 0.825

Review 4.  Hereditary Angioedema with Normal C1 Inhibitor: Update on Evaluation and Treatment.

Authors:  Markus Magerl; Anastasios E Germenis; Coen Maas; Marcus Maurer
Journal:  Immunol Allergy Clin North Am       Date:  2017-08       Impact factor: 3.479

Review 5.  Emerging Therapies in Hereditary Angioedema.

Authors:  Meng Chen; Marc A Riedl
Journal:  Immunol Allergy Clin North Am       Date:  2017-08       Impact factor: 3.479

Review 6.  Acquired C1 Inhibitor Deficiency.

Authors:  Iris M Otani; Aleena Banerji
Journal:  Immunol Allergy Clin North Am       Date:  2017-05-15       Impact factor: 3.479

7.  Hereditary angioedema: new findings concerning symptoms, affected organs, and course.

Authors:  Konrad Bork; Gabriele Meng; Petra Staubach; Jochen Hardt
Journal:  Am J Med       Date:  2006-03       Impact factor: 4.965

8.  An evaluation of tests used for the diagnosis and monitoring of C1 inhibitor deficiency: normal serum C4 does not exclude hereditary angio-oedema.

Authors:  M D Tarzi; A Hickey; T Förster; M Mohammadi; H J Longhurst
Journal:  Clin Exp Immunol       Date:  2007-07-05       Impact factor: 4.330

9.  Hereditary and acquired C1-inhibitor deficiency: biological and clinical characteristics in 235 patients.

Authors:  A Agostoni; M Cicardi
Journal:  Medicine (Baltimore)       Date:  1992-07       Impact factor: 1.889

10.  Hereditary angioedema caused by c1-esterase inhibitor deficiency: a literature-based analysis and clinical commentary on prophylaxis treatment strategies.

Authors:  Richard G Gower; Paula J Busse; Emel Aygören-Pürsün; Amin J Barakat; Teresa Caballero; Mark Davis-Lorton; Henriette Farkas; David S Hurewitz; Joshua S Jacobs; Douglas T Johnston; William Lumry; Marcus Maurer
Journal:  World Allergy Organ J       Date:  2011-02       Impact factor: 4.084

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  1 in total

1.  The international WAO/EAACI guideline for the management of hereditary angioedema - The 2021 revision and update.

Authors:  Marcus Maurer; Markus Magerl; Stephen Betschel; Werner Aberer; Ignacio J Ansotegui; Emel Aygören-Pürsün; Aleena Banerji; Noémi-Anna Bara; Isabelle Boccon-Gibod; Konrad Bork; Laurence Bouillet; Henrik Balle Boysen; Nicholas Brodszki; Paula J Busse; Anette Bygum; Teresa Caballero; Mauro Cancian; Anthony J Castaldo; Danny M Cohn; Dorottya Csuka; Henriette Farkas; Mark Gompels; Richard Gower; Anete S Grumach; Guillermo Guidos-Fogelbach; Michihiro Hide; Hye-Ryun Kang; Allen P Kaplan; Constance H Katelaris; Sorena Kiani-Alikhan; Wei-Te Lei; Richard F Lockey; Hilary Longhurst; William Lumry; Andrew MacGinnitie; Alejandro Malbran; Inmaculada Martinez Saguer; Juan José Matta Campos; Alexander Nast; Dinh Nguyen; Sandra A Nieto-Martinez; Ruby Pawankar; Jonathan Peter; Grzegorz Porebski; Nieves Prior; Avner Reshef; Marc Riedl; Bruce Ritchie; Farrukh Rafique Sheikh; William B Smith; Peter J Spaeth; Marcin Stobiecki; Elias Toubi; Lilian Agnes Varga; Karsten Weller; Andrea Zanichelli; Yuxiang Zhi; Bruce Zuraw; Timothy Craig
Journal:  World Allergy Organ J       Date:  2022-04-07       Impact factor: 5.516

  1 in total

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