Angioedema (AE) is related to the activation of the contact phase system-kallikrein and generation of bradykinin. Different types of AE are recognized: hereditary or acquired deficit of the C1 inhibitor, drug-related, or idiopathic. Treatment of idiopathic nonhistaminergic AE (IAE) is difficult because corticosteroids, antihistamine drugs, and adrenalin are inefficacious. We describe a patient with an IAE and an acute attack of facial AE that was successfully treated with the bradykinin receptor antagonist icatibant. This case report strengthens the relevance of bradykinin formation in IAE and underlines the effectiveness of icatibant as a therapeutic option in acute IAE. © 2013 Elsevier Inc. All rights reserved
The absolute risk of angiotensin-converting enzyme (ACE) inhibitor angioedema is 0.3 % [1]. The mech...
type I in a female patient: a case report Hereditary angioedema (HAE) is rare autosomal dominant dis...
Hereditary angioedema is a disease which develops as a result of a deficiency or dysfonction of C1-i...
Angioedema (AE) is related to the activation of the contact phase system-kallikrein and generation o...
Angioedema (AE) is related to the activation of the contact phase system—kallikrein and generation o...
BACKGROUND Hereditary angioedema is characterized by recurrent attacks of angioedema of the skin, l...
BACKGROUND: In hereditary angioedema, bradykinin is assumed to be the most important mediator of ede...
BACKGROUND Hereditary angioedema is characterized by recurrent attacks of angioedema of the skin, la...
Abstract Current strategies for the treatment of hereditary angioedema (HAE) include targeted inhibi...
Icatibant, a bradykinin B2 receptor antagonist, is an established treatment for acute attacks of her...
Background: Angioedema occurs in up to 2% of those taking angiotensin-converting enzyme (ACE) inhibi...
Introduction: Hereditary Angioedema (HAE) is a potentially life-threatening condition consisting of ...
Icatibant, an antagonist of the bradykinin B2 receptor, was a approved for the treatment of acute at...
Abstract Acquired angioedema (AAE) is characterized by acquired deficiency of C1 inhibitor (C1-INH),...
Hereditary angioedema (HAE) is arare, potentially life-threatening au-tosomal dominant disease cause...
The absolute risk of angiotensin-converting enzyme (ACE) inhibitor angioedema is 0.3 % [1]. The mech...
type I in a female patient: a case report Hereditary angioedema (HAE) is rare autosomal dominant dis...
Hereditary angioedema is a disease which develops as a result of a deficiency or dysfonction of C1-i...
Angioedema (AE) is related to the activation of the contact phase system-kallikrein and generation o...
Angioedema (AE) is related to the activation of the contact phase system—kallikrein and generation o...
BACKGROUND Hereditary angioedema is characterized by recurrent attacks of angioedema of the skin, l...
BACKGROUND: In hereditary angioedema, bradykinin is assumed to be the most important mediator of ede...
BACKGROUND Hereditary angioedema is characterized by recurrent attacks of angioedema of the skin, la...
Abstract Current strategies for the treatment of hereditary angioedema (HAE) include targeted inhibi...
Icatibant, a bradykinin B2 receptor antagonist, is an established treatment for acute attacks of her...
Background: Angioedema occurs in up to 2% of those taking angiotensin-converting enzyme (ACE) inhibi...
Introduction: Hereditary Angioedema (HAE) is a potentially life-threatening condition consisting of ...
Icatibant, an antagonist of the bradykinin B2 receptor, was a approved for the treatment of acute at...
Abstract Acquired angioedema (AAE) is characterized by acquired deficiency of C1 inhibitor (C1-INH),...
Hereditary angioedema (HAE) is arare, potentially life-threatening au-tosomal dominant disease cause...
The absolute risk of angiotensin-converting enzyme (ACE) inhibitor angioedema is 0.3 % [1]. The mech...
type I in a female patient: a case report Hereditary angioedema (HAE) is rare autosomal dominant dis...
Hereditary angioedema is a disease which develops as a result of a deficiency or dysfonction of C1-i...