Hereditary angioedema on the occasion of a pediatric case: Bir çocuk olgu nedeniyle herediter anjioödem

Hakan  Turan; Mesut Okur; Ersoy Acer; Zehra Gürlevik; Mehmet Emin Yanık

doi:10.5455/GMJ-30-2011-23

Authors

Hakan Turan Düzce Üniversitesi, Tıp Fakültesi, Dermatoloji Anabilim Dalı, Düzce
Mesut Okur Düzce Üniversitesi, Tıp Fakültesi, Çocuk Sağlığı ve Hastalıkları Anabilim Dalı, Düzce
Ersoy Acer Düzce Üniversitesi, Tıp Fakültesi, Dermatoloji Anabilim Dalı, Düzce
Zehra Gürlevik Düzce Üniversitesi, Tıp Fakültesi, Dermatoloji Anabilim Dalı, Düzce
Mehmet Emin Yanık Düzce Üniversitesi, Tıp Fakültesi, Dermatoloji Anabilim Dalı, Düzce

DOI:

https://doi.org/10.5455/GMJ-30-2011-23

Keywords:

Hereditary angioedema, fresh frozen plasma, treatment

Abstract

Hereditary angioedema is a rare and life threatening autosomal-dominant disorder which results from the congenital deficiency of C1- esterase inhibitor. It is responsible for approximately 2% of all angioedema cases. Recurring angioedema attacks that involve subcutaneous and submucosal areas are the hallmarks of hereditary angioedema. Here, we review the clinical findings and therapeutic approaches of the disease by presenting a 5-years old female patient with severe extremity edema who was diagnosed as hereditary angioedema and treated with fresh frozen plasma.

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