HEREDITARY ANGIOEDEMA - Pancreatitis? - CLINICAL CASE

2018 ◽  
Author(s):  
Tatiana  Lourenço
Keyword(s):  
Hereditary Angioedema ◽  
Clinical Case

scholarly journals HEREDITARY ANGIOEDEMA IN CHILDREN — A RARE CLINICAL CASE IN THE PRACTICE OF THE ABDOMINAL SURGEON

2014 ◽  
Vol 13 (5) ◽  
pp. 97
Author(s):  
Ye. Yu. Dyakonova ◽  
I. V. Poddubny ◽  
N. V. Nikitina ◽  
А. S. Bekin ◽  
Т. V. Kuznetsova ◽  
...  
Keyword(s):  
Hereditary Angioedema ◽  
Clinical Case

scholarly journals Features of diagnostics and clinical approaches to case management of patients with hereditary angioedema without C1 esterase inhibitor deficiency. Analysis of the clinical case

2020 ◽  
Vol 17 (1) ◽  
pp. 58-65
Author(s):  
Daria S Fomina ◽  
Elena N Bobrikova ◽  
Sofia A Serdotetskova
Keyword(s):  
Case Management ◽  
Hereditary Angioedema ◽  
Clinical Case ◽  
Medical Society ◽  
Differential Diagnostics ◽  
Factor Xii ◽  
C1 Esterase Inhibitor ◽  
Primary Diagnostics ◽  
Genetic Features ◽  
Esterase Inhibitor

This article describes the clinical, biochemical and genetic features of hereditary angioedema (HAE) with normal level and functional activity of C1 esterase inhibitor. The discussion includes pathogenesis, diagnostics and case management of patients with hereditary angioedema without C1 esterase inhibitor deficiency. The materials of few scientific sources about patients with HAE without C1 esterase inhibitor deficiency in stages and our own clinical case (the female patient of fertile age with a confirmed mutation associated with factor XII (Hageman) deficiency) was given. The article describes the current state of the issue of the algorithm of primary diagnostics and differential diagnostics of HAE without C1 esterase inhibitor deficiency based on international and Russian data. It has been suggested that the new understanding of pathogenesis and treatment of patients with HAE without C1 esterase inhibitor deficiency is encouraging and becoming accessible to the medical society.

scholarly journals Features of diagnostics and clinical approaches to case management of patients with hereditary angioedema without C1 esterase inhibitor deficiency. Analysis of the clinical case

2020 ◽  
Vol 17 (1) ◽  
pp. 58-65
Author(s):  
Daria S Fomina ◽  
Elena N Bobrikova ◽  
Sofia A Serdotetskova
Keyword(s):  
Case Management ◽  
Hereditary Angioedema ◽  
Clinical Case ◽  
Medical Society ◽  
Differential Diagnostics ◽  
Factor Xii ◽  
C1 Esterase Inhibitor ◽  
Primary Diagnostics ◽  
Genetic Features ◽  
Esterase Inhibitor

This article describes the clinical, biochemical and genetic features of hereditary angioedema (HAE) with normal level and functional activity of C1 esterase inhibitor. The discussion includes pathogenesis, diagnostics and case management of patients with hereditary angioedema without C1 esterase inhibitor deficiency. The materials of few scientific sources about patients with HAE without C1 esterase inhibitor deficiency in stages and our own clinical case (the female patient of fertile age with a confirmed mutation associated with factor XII (Hageman) deficiency) was given. The article describes the current state of the issue of the algorithm of primary diagnostics and differential diagnostics of HAE without C1 esterase inhibitor deficiency based on international and Russian data. It has been suggested that the new understanding of pathogenesis and treatment of patients with HAE without C1 esterase inhibitor deficiency is encouraging and becoming accessible to the medical society.

scholarly journals ANGIONEUROTIC EDEMA IN A PATIENT WITH HEREDITARY ANGIOEDEMA TYPE I, INDUCED BY AN OPIOID ANALGESIC - A CLINICAL CASE.

2017 ◽  
Vol 5 (9) ◽  
pp. 1376-1381
Author(s):  
Dermrndjiev Sv ◽  
◽  
Koev K ◽  
Dermendjiev T ◽  
◽  
...  
Keyword(s):  
Hereditary Angioedema ◽  
Clinical Case ◽  
Opioid Analgesic ◽  
Type I ◽  
Angioneurotic Edema

scholarly journals Anesthetic considerations for a patient with hereditary angioedema – A clinical case

2017 ◽  
Vol 67 (5) ◽  
pp. 541-543
Author(s):  
Maria J.L. Vilaça ◽  
Filipa M. Coelho ◽  
Ana Faísco ◽  
Cristina Carmona
Keyword(s):  
Hereditary Angioedema ◽  
Clinical Case ◽  
Anesthetic Considerations

scholarly journals Complex clinical case: hereditary angioedema

2021 ◽  
Vol 5 (1) ◽  
pp. 50-53
Author(s):  
E.A. Sobko ◽  
◽  
I.V. Demko ◽  
I.A. Solovieva ◽  
A.Yu. Kraposhina ◽  
...  
Keyword(s):  
Hereditary Angioedema ◽  
Clinical Case ◽  
Psychological Symptoms ◽  
Disease Onset ◽  
Final Diagnosis ◽  
C1 Inhibitor ◽  
Surgical Interventions ◽  
Life Threatening ◽  
Promising Treatment ◽  
Russian Medical

Nowadays, isolated angioedema is one of the most complex and urgent problems of modern allergology and immunology. Hereditary angioedema (HA) refers to orphan and life-threatening diseases associated with a deficiency or decrease in C1-inhibitor function and is characterized by recurrent edema in deep dermis of various localization. A doctor of any specialty can encounter this nosology, which obliges all medical officers to have a general overview concerning HA. Late diagnosis is fraught with unnecessary surgical interventions, psychological symptoms, opiate addiction, or life-threatening laryngeal angioedema. To date, the final diagnosis of HA, and, consequently, adequate drug therapy, is delayed by an average of 8.5 years from disease onset. Sudden edema in the vital organs is a source of constant anxiety, a cause of disability, and sometimes fatal outcomes. The article presents a clinical case and discusses therapy principles, existing possibilities of promising treatment and recommendations for further management. KEYWORDS: hereditary angioedema, recurrent edema, orphan diseases, bradykinin; C1-inhibitor; complement system. FOR CITATION: Sobko E.A., Demko I.V., Solovieva I.A. et al. Complex clinical case: hereditary angioedema. Russian Medical Inquiry. 2021;5(1):50–53. DOI: 10.32364/2587-6821-2021-5-1-50-53.

Features and difficulties of management of children with hereditary angioedema (a clinical case report)

2021 ◽  
Vol 87 (1) ◽  
pp. 56-58
Author(s):  
V.Yu. Tarasevich ◽  
Keyword(s):  
Quality Of Life ◽  
Hereditary Angioedema ◽  
Clinical Case ◽  
Clinical Situation ◽  
Main Role ◽  
Disease Treatment ◽  
Complete Control ◽  
Severity Of The Disease ◽  
The Complement System

Hereditary angioedema (HAE) refers to primary immunodeficiencies without an infectious syndrome. In the pathogenesis of this disease, the main role is played by violations in the complement system. Although HAE is a rare disease, it potentially threatens the patient's life and significantly affects the quality of life. Therefore, it is necessary to achieve complete control over the disease. Treatment of HAE requires an individual approach depending on the severity of the disease and the clinical situation

The Variable Nature of Stuttering: A Clinical Case Study

1995 ◽  
Vol 22 ◽  
pp. 29-35
Author(s):  
Jennifer Gutierrez ◽  
Anthony Caruso
Keyword(s):  
Clinical Case ◽  
Clinical Case Study ◽  
Variable Nature

Hereditary Angioedema Diagnostic Delay Can Kill

2007 ◽  
Vol 41 (4) ◽  
pp. 45
Author(s):  
ROBERT FINN
Keyword(s):  
Hereditary Angioedema ◽  
Diagnostic Delay

Icatibant Promising for Hereditary Angioedema

2007 ◽  
Vol 38 (7) ◽  
pp. 8
Author(s):  
NANCY WALSH
Keyword(s):  
Hereditary Angioedema
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