Diagnosis and treatment of hereditary angioedema: An expert opinion

被引:2
|
作者
Jung, Jae-Woo [1 ]
Park, So-Young [1 ]
Yoon, Sun Young [2 ]
Kim, Gun-Woo [3 ]
Sohn, Kyoung-Hee [4 ]
Kang, Sung-Yoon [5 ]
Park, Hye Jung [6 ]
Kang, Min-Kyu [7 ]
Kim, Joo-Hee [8 ]
Park, Kyung Hee [9 ,10 ]
Suh, Dong In [11 ,12 ]
Lee, Dong Hun [13 ]
Kim, Sae-Hoon [14 ]
Kwon, Hyouk-Soo [15 ]
Kang, Hye-Ryun [16 ,17 ]
机构
[1] Chung Ang Univ, Coll Med, Dept Internal Med, Seoul, South Korea
[2] Chungnam Natl Univ, Sejong Hosp, Dept Internal Med, Div Pulmonol & Allergy, Sejong, South Korea
[3] St Carollo Gen Hosp, Dept Internal Med, Sunchon, South Korea
[4] Kyung Hee Univ, Med Ctr, Dept Internal Med, Div Pulmonol & Allergy, Seoul, South Korea
[5] Gachon Univ, Gil Med Ctr, Dept Internal Med, Div Pulmonol & Allergy, Incheon, South Korea
[6] Yonsei Univ, Coll Med, Gangnam Severance Hosp, Dept Internal Med, Seoul, South Korea
[7] Chungbuk Natl Univ Hosp, Chungbuk Natl Coll Med, Dept Internal Med, Cheongju, South Korea
[8] Hallym Univ, Sacred Heart Hosp, Coll Med, Div Pulm Allergy & Crit Care Med, Anyang, South Korea
[9] Yonsei Univ, Coll Med, Dept Internal Med, Seoul, South Korea
[10] Yonsei Univ, Coll Med, Inst Allergy, Seoul, South Korea
[11] Seoul Natl Univ Hosp, Dept Pediat, Seoul, South Korea
[12] Seoul Natl Univ, Coll Med, Dept Pediat, Seoul, South Korea
[13] Seoul Natl Univ, Coll Med, Dept Dermatol, Seoul, South Korea
[14] Seoul Natl Univ, Bundang Hosp, Dept Internal Med, Seongnam, South Korea
[15] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Allergy & Clin Immunol, Seoul, South Korea
[16] Seoul Natl Univ, Med Res Ctr, Inst Allergy & Clin Immunol, Seoul, South Korea
[17] Seoul Natl Univ, Coll Med, Dept Internal Med, 20 Boramae Ro 5 Gil, Seoul 07061, South Korea
来源
ALLERGY ASTHMA & RESPIRATORY DISEASE | 2022年 / 10卷 / 02期
关键词
Hereditary angioedema; Bradykinin; C1-inhibitor; Diagnosis; Management; PRODROMAL SYMPTOMS; C1-INHIBITOR CONCENTRATE; ANGIONEUROTIC-EDEMA; INHIBITOR; PROPHYLAXIS; ICATIBANT; EFFICACY; PATIENT; DEFICIENCY; DANAZOL;
D O I
10.4168/aard.2022.10.2.80
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Hereditary angioedema (HAE) is a rare disease, but it severely interrupts daily life activities and can sometimes be life-threatening. Therefore, early diagnosis and prompt treatment of HAE attacks are critical. Physicians should be aware of how to diagnose and manage HAE to prepare not to miss a diagnosis when treating HAE patients. Physicians must also carry out tests to confirm the diagnosis of HAEs caused by C1 inhibitor deficiency (type 1) or C1 inhibitor dysfunction (type 2) in patients with recurrent angioedema. In addition, recent studies revealed another type of HAE which is not related to Cl inhibitor (normal C1 inhibitor HAE). Once HAE is confirmed, patients and their caregivers should be given with short-term and long-term treatment plans to relieve or prevent HAE attacks. HAE requires life-long measures, including psychological support for patients and self-management education.
引用
收藏
页码:80 / 88
页数:9
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