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Hereditary angioedema –  neglected diagnosis


Authors: P. Králíčková 1;  E. Burešová 1;  T. Freiberger 2;  I. Tachecí 3
Authors‘ workplace: Ústav klinické imunologie a alergologie Lékařské fakulty UK a FN Hradec Králové, přednosta prof. RNDr. Jan Krejsek, CSc. 1;  Genetická laboratoř Centra kardiovaskulární a transplantační chirurgie Brno, ředitel doc. MU Dr. Petr Němec, CSc., FETCS 2;  Oddělení gastroenterologie a hepatologie, vedoucí prof. MU Dr. Jan Bureš, CSc., II. interní kliniky Lékařské fakulty UK a FN Hradec Králové, přednosta prof. MU Dr. Jaroslav Malý, CSc. 3
Published in: Vnitř Lék 2010; 56(9): 927-931
Category: Case Reports

Overview

Hereditary angioedema caused by C1 esterase inhibitor deficiency is a rare autosomal dominant inherited disorder. It is cha­racterized by reccurent episodes of potentially life‑ threatening swellings without itching localized in the dermis and submucosa. We report a case of 41 years old woman with hereditary angioedema manifested as episodes of localized skin swellings and painful gastrointestinal colics. This report underlines the fact that hereditary angioedema is underdiagnosed in differential diagnoses. If hereditary angioedema is correctly diagnosed, effective treatment highly improving patients’ quality of life is available.

Key words:
angioedema –  C1 inhibitor –  danazol


Sources

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Labels
Allergology and clinical immunology Diabetology Endocrinology Internal medicine

Article was published in

Internal Medicine

Issue 9

2010 Issue 9

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