Hereditary angioedema, a battle for an accurate diagnosis

Authors

  • Lay Salazar Torres Policlínico "Chiqui Gómez Lubián", Santa Clara, Villa Clara
  • Carmen Díaz Marín Policlínico "Chiqui Gómez Lubián", Santa Clara, Villa Clara
  • Frank Quintana Gómez Universidad de Ciencias Médicas “Dr. Serafín Ruiz de Zárate Ruiz” de Villa Clara

Keywords:

angioedema, diagnosis

Abstract

 

 

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Author Biographies

Lay Salazar Torres, Policlínico "Chiqui Gómez Lubián", Santa Clara, Villa Clara

Especialista de I y II Grado en Inmunología. Máster en Atención Integral al Niño. Investigadora Agregada.
Profesora Asistente de la Universidad de Ciencias Médicas de Villa Clara.

Carmen Díaz Marín, Policlínico "Chiqui Gómez Lubián", Santa Clara, Villa Clara

Especialista de I Grado en Alergia

Frank Quintana Gómez, Universidad de Ciencias Médicas “Dr. Serafín Ruiz de Zárate Ruiz” de Villa Clara

Especialista de I Grado en Inmunología. Máster en Educación Médica.
Profesor Auxiliar de la Universidad de Ciencias Médicas de Villa Clara.

References

1. Velasco-Medina AA, Cortés-Morales G, Barreto-Sosa A, Velázquez-Sámano G. Fisiopatología y avances en el tratamiento del Angioedema Hereditario. Rev Alerg Méx [Internet]. 2011 [citado 2 Oct 2014];58(2):112-119. Disponible en: http://www.elsevier.es/es-revista-revista-alergia-mexico-336-articulo-fisiopatologia-avances-el-tratamiento-del-90024068

2. Navarro Ruiz A, Crespo Diz C, Poveda Andrés JL, Cebollero de Torre A. Algoritmo de diagnóstico y tratamiento del angioedema hereditario como herramienta para su manejo. Farm Hosp [Internet]. 2013 [citado 9 Abr 2014];37(6):521-529. Disponible en: http://scielo.isciii.es/pdf/fh/v37n6/12articuloespecial02.pdf

3. Caballero T, Farkas H, Bouillet L, Bowen T, Gompel A, Fagerberg C, et al. International consensus and practical guidelines on the gynecologic and obstetric management of female patients with hereditary angioedema caused by C1 inhibitor deficiency. J Allergy Clin Immunol [Internet]. 2012 [citado 2 Oct 2014]; 129(2): 308-20. Disponible en: http://www.ncbi.nlm.nih.gov/pubmed/22197274

4. Wasserman SI. Approach to the person with allergic or immunologic disease. En: Goldman L, Schafer AI, eds. Cecil Medicine. 24th ed. Philadelphia, PA: Saunders Elsevier; 2011. p. 257.

5. Salas-Lozano NG, Meza-Cardona J, González-Fernández C, Pineda-Figueroa L, De Ariño-Suárez M. Angioedema hereditario: causa rara de dolor abdominal. Cir Cir [Internet]. 2014 [citado 9 Abr 2014];82(5):563-566. Disponible en: http://www.medigraphic.com/pdfs/circir/cc-2014/cc145m.pdf

6. Malbrán A, Fernández Romero DS, Menéndez A. Angioedema hereditario. Guía de tratamiento. Medicina (B. Aires) [Internet]. 2012 [citado 2 Oct 2014];72(2):119-23. Disponible en: http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0025-76802012000200006

7. Zuraw BL, Banerji A, Bernstein JA, Busse PJ, Christiansen SC, Davis-Lorton M, et al. US Hereditary Angioedema Association Medical Advisory Board 2013 recommendations for the management of hereditary angioedema due to C1 inhibitor deficiency. J Allergy Clin Imunol Pract [Internet]. 2013 [citado 9 Oct 2014];1(5):458-67. Disponible en: http://www.ncbi.nlm.nih.gov/pubmed/24565617

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How to Cite

1.
Salazar Torres L, Díaz Marín C, Quintana Gómez F. Hereditary angioedema, a battle for an accurate diagnosis. Acta Méd Centro [Internet]. 2015 Dec. 23 [cited 2025 Jun. 28];9(4):82-4. Available from: https://revactamedicacentro.sld.cu/index.php/amc/article/view/297

Issue

Vol. 9 No. 4 (2015): October-December

Section

Letters to the Editor

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