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Acta Médica del Centro

ISSN 1995-9494 (Electronic)
Revista del Hospital Clínico Quirúrgico "Arnaldo Milián Castro"
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2014, Number 3

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Acta Med Cent 2014; 8 (3)

Quincke's disease, challenge of the Specialist in Otorhinolaryngology

Rodríguez LM, Sarduy BL, Corrales ÁM
Full text How to cite this article

Language: Spanish
References: 10
Page: 136-140
PDF size: 65.70 Kb.


Key words:

angioedema.

ABSTRACT

Quincke's disease or hereditary angioedema is a genetic disease caused by the functional deficiency of the enzyme C1 inhibitor. It is a rare desease of autosomal dominant transmission , characterized by recurrent self-limiting episodes of angioedema. Its incidence is estimated from 1:10 000 to 1:50 000 habitants, it has been described in all races and affects both sexes equally and attacks affect the skin, abdomen and pharynx or larynx. Cuba, especially the province of Villa Clara, have been affected in recent years by the presence of patients suffering this disease. The rapid diagnosis, based on a proper physical examination, and appropriate treatment are essential tools to avoid complications. A call is made on the medical act in this health situation in order to preserve the most precious treasure, life.


REFERENCES

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  2. Nussberger J, Cugno M, Cicardi M. Bradykinin-mediated angioedema. N Engl J Med. 2002;347:621-2.

  3. Han ED, MacFarlane RC, Mulligan AN, Scafidi J, Davis AE III. Increased vascular permeability in C1 inhibitor-deficient mice mediated by the bradykinin type 2 receptor. J Clin Invest 2002;109:1057-63.

  4. Bowen T, Cicardi M, Fakas H. Canadian 2008 International Consensus Algorithm for the diagnosis, therapy and management of hereditary angioedema. J Allergy Clin Immunol. 2004;114:629-37.

  5. Bowen T, Cicardi M, Bork K. 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. Ann Allergy Asthma Immunolog. 2008 Jan;100(1 Suppl 2):S30-S40.

  6. Bowen T, Cicardi M, Farkas H. 2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema. Allergy Asthma Clin Immunol. 2010;6(1):24-37.

  7. Cicardi M, Bork K, Caballero T. On behalf of HAWK (Hereditary Angioedema International Working Group). Evidence-based recommendations for the therapeutic management of angioedema due to hereditary C1- inhibitor deficiency. Consensus report of an International Working Group. Allergy. 2012;67:147-57.

  8. Fernández Romero DS, Di Marco P, Malbrán A. Angioedema Hereditario. Historia familiar y manifestaciones clínicas en 58 pacientes. Medicina (B Aires). 2009;69:601-6.

  9. Craig TJ, Levy RJ, Wasserman RL. Efficacy of human C1 esterase inhibitor concentrate compared with placebo in acute hereditary angioedema attacks. J Allergy Clin Immunol. 2009 Oct;124(4):801-8. doi:10.1016/j.jaci.2009.07.017.

  10. Zuraw BL, Busse PJ, White M. Nanofiltered C1 inhibitor concentrate for treatment of hereditary angioedema. N Engl J Med. 2010 Aug 5;363:513-22 doi: 10.1056/NEJMoa0805538




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Acta Med Cent. 2014;8