Hereditary Angioedema: Implications of Management

被引:3
作者
Pathria, Mohini [1 ]
Krishnaswamy, Guha
Guarderas, Juan C.
机构
[1] Univ Florida, Dept Internal Med, 2000 SW Archer Rd, Gainesville, FL 32608 USA
关键词
C1 esterase inhibitor; C1 esterase inhibitor deficiency; C1 inhibitor deficiency; hereditary angioedema; ANGIONEUROTIC-EDEMA; C1; INHIBITOR; FROZEN PLASMA; ACUTE ATTACKS; C1-INHIBITOR; DEFICIENCY; SYMPTOMS; THERAPY; GENE; PROPHYLAXIS;
D O I
10.14423/SMJ.0000000000000604
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hereditary angioedema (HAE) is a genetic condition that is characterized by frequent episodes of localized angioedema. It is a rare disorder that a primary care provider, otolaryngologist, dermatologist, or rheumatologist may encounter only occasionally. This disease is being reviewed because of the significant advances in further understanding the genetics, biology, and therapeutic management surrounding the condition. Histamine-mediated angioedema responds to steroids, antihistamines, and epinephrine, whereas bradykinin-mediated angioedema is resistant to those interventions and requires specialized therapy. Previously used medications have significant adverse effects. Approved medications for HAE have been effective in decreasing morbidity and mortality in patients with this condition. We review the presentation, diagnosis, and available pharmaceutical options for HAE and explore the limitations of implementing recommended therapy.
引用
收藏
页码:101 / 106
页数:6
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