Results 21 to 30 of about 636 (203)
Revista Alergia México, 2016 Angioedema is defined as edema of the skin or mucosa, including the respiratory and the gastrointestinal mucosa, which is self-limiting, and in most cases is completely resolved in less than 72 hours. It occurs due to increased permeability of the mucosal and submucosal capillaries and postcapillary venules, with resulting plasma extravasation.
Holguín Gómez, Luisa +2 more
openaire +6 more sources
, 2020 BfArM’s ADR-database analysis: Stratified analysis of anatomical areas affected by ACEi-associated angioedemas.
Diana Dubrall (8626530) +3 more
core +1 more source
Cureus, 2023 The authors present the case of a 22-year-old female who reported having a persistent sore throat. The patient had a history of recurring episodes of hereditary angioedema and arrived at the emergency department with her C1-esterase inhibitor. The epidemiology, clinical presentation, and treatment strategies are presented.
Banerjee, Anjali +4 more
openaire +2 more sources
BfArM’s ADR-database analysis: "Time-to-onset" analysis of the angioedema reaction.
, 2020 Fig 4 shows the "time-to-onset" analysis of validated ACEi, ARBs, and aliskiren-associated angioedemas. In this figure only cases providing information on the "time-to-onset" were included.
Diana Dubrall (8626530) +3 more
core +1 more source
BRADYKININ MEDIATED ANGIOEDEMA DURING PREGNANCY CASE REPORT
, 2022 Angioedemaisdefined as a non-inflammatory, localized, transientedema of the subcutaneous and/or submucosal tissues, thatappearswithin a few hours and disappearscompletelyafter the attack.
Badsi Safae , Louzali Fatima Zohra , Benaouicha Nisrine , Zeraidi Najia , Lakhdar Amina , Kharbache Aicha and Baidada Aziz
core +1 more source
Allergy, Asthma & Clinical Immunology, 2010 Acquired angioedema (AAE) is characterized by acquired deficiency of C1 inhibitor (C1-INH), hyperactivation of the classical pathway of human complement and angioedema symptoms mediated by bradykinin released by inappropriate activation of the contact-kinin system.
M. Cicardi, A. Zanichelli
openaire +3 more sources
International Journal of Emergency Medicine, 2021 AbstractA 14-year-old African American female presented to the emergency department with spontaneous, sudden-onset lip swelling for 1 h. On examination, there was significant water-bag edema of the upper lip extending to the philtrum and premaxilla. Nasopharyngeal laryngoscopy revealed a patent airway without edema.
Helen Lesser, Jason E. Cohn
openaire +3 more sources
Acta Médica Portuguesa, 2019 Introduction: Hospitalizations due to angioedema are important especially in debilitating or life-threatening situations. The aim of this study was to evaluate the frequency and etiology of angioedema without urticaria in hospital admissions.
Joana Cosme +3 more
doaj +1 more source
Screening for Plasminogen Mutations in Hereditary Angioedema Patients
, 2021 Hereditary angioedema (HAE) is a rare disease belonging to the group of bradykinin-mediated angioedemas, characterized by recurring edematous episodes involving the subcutaneous and/or submucosal tissues.
Edina Szabó +4 more
core +1 more source
Allergy, Asthma & Clinical ImmunologyAbstract Angioedema can occur in the absence of urticaria and can be broadly divided into three main categories: mast cell-mediated (e.g., histamine), non-mast-cell-mediated (bradykinin-induced) and idiopathic angioedema. Non-mast-cell-mediated angioedema is largely driven by bradykinin.
Gina Lacuesta +3 more
openaire +3 more sources