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Update on management of pediatric atopic dermatitis 儿童特应性皮炎的治疗进展
IF 0.2 Pub Date : 2021-01-01 DOI: 10.4168/aard.2021.9.2.59
Y. H. Jeon, J. Kim
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引用次数: 1
호산구증다증과 동반된 비삽화성 혈관부종의 1예 一种非插画性血管水肿伴有嗜酸性粒细胞增多症
IF 0.2 Pub Date : 2021-01-01 DOI: 10.4168/AARD.2021.9.1.46
최 지웅, 박 소영, 문 경태, 이 원미, 이 병훈, 김 상훈
Nonepisodic angioedema with eosinophilia (NEAE) is a rare disease characterized by nonrecurrent angioedema with eosinophilia and normal serum IgM levels occurring predominantly in an East Asian female population. A 49-year-old male patient visited our clinic due to swelling of both the scrotums and the lower extremities, and fever. He had history of nasal polyp, cephalosporin allergy, and asthma. He was diagnosed as having NEAE and was treated with systemic corticosteroid, then he was symptom-free for more than 8 months. He had been administered omalizumab for 3 months due to uncontrolled asthma prior to the onset of angioedema which had helped taper the oral corticosteroid, and this may be associated with presentation of NEAE. Here, we report a case of NEAE in a male patient which presented with constitutional symptoms such as fever and scrotal edema. (Allergy Asthma Respir Dis 2021;9:46-49)
非发作性血管性水肿伴嗜酸性粒细胞增多(NEAE)是一种罕见的疾病,以非复发性血管性水肿伴嗜酸性粒细胞增多和血清IgM水平正常为特征,主要发生在东亚女性人群中。患者男,49岁,因阴囊及下肢肿胀及发热就诊。有鼻息肉史、头孢菌素过敏史、哮喘史。经诊断为NEAE,全身性皮质类固醇治疗后症状消失8个多月。在血管性水肿发作之前,由于哮喘不受控制,他服用了3个月的奥玛珠单抗,这有助于减少口服皮质类固醇,这可能与NEAE的出现有关。在此,我们报告一例NEAE的男性患者,其表现为发热和阴囊水肿等体质症状。(过敏哮喘呼吸疾病2021;9:46-49)
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引用次数: 0
Effects of an electronic system for the management of adverse reactions to iodinated contrast media 电子系统对碘化造影剂不良反应管理的影响
IF 0.2 Pub Date : 2021-01-01 DOI: 10.4168/aard.2021.9.3.164
Eun-Jung Jo, Hye-Kyung Park
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引用次数: 0
Lung function decline in adult; when does it begin? 成人肺功能下降;什么时候开始?
IF 0.2 Pub Date : 2021-01-01 DOI: 10.4168/aard.2021.9.2.57
Heung-Woo Park
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引用次数: 0
Evaluation of sleep-disordered breathing in children with Prader-Willi syndrome: Polysomnography Prader-Willi综合征儿童睡眠呼吸障碍的评估:多导睡眠描记术
IF 0.2 Pub Date : 2021-01-01 DOI: 10.4168/aard.2021.9.4.187
E. Kang
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引用次数: 0
Severe laryngomalacia in a 1-month infant with Marfan syndrome 1个月马凡氏综合征婴儿的严重喉软化
IF 0.2 Pub Date : 2021-01-01 DOI: 10.4168/AARD.2021.9.1.42
S. Moon, H. C. Yang, E. Song, Y. Choi, Eun Lee
Correspondence to: Eun Lee https://orcid.org/0000-0002-0145-7067 Department of Pediatrics, Chonnam National University Hospital, Chonnam National University Medical School, 42 Jebong-ro, Dong-gu, Gwangju 61469, Korea Tel: +82-62-220-6649, Fax: +82-62-222-6103, Email: unelee@daum.net Received: April 12, 2020 Revised: June 29, 2020 Accepted: June 29, 2020 © 2021 The Korean Academy of Pediatric Allergy and Respiratory Disease The Korean Academy of Asthma, Allergy and Clinical Immunology This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/). 마르판증후군이 있는 1개월 영아에서 동반된 중증 후두연화증
通讯作者:Eun Lee https://orcid.org/0000-0002-0145-7067韩国光州东区济峰路42号全南大学医学院全南大学医院儿科电话:+82-62-220-6649,传真:+82-62-222-6103,Email: unelee@daum.net收稿日期:2020年4月12日修订日期:2020年6月29日接受:2020年6月29日©2021韩国儿科过敏和呼吸道疾病学会韩国哮喘,过敏和临床免疫学学会这是一篇开放获取文章,根据知识共享署名非商业许可(https://creativecommons.org/licenses/by-nc/4.0/)的条款分发。■1■■■■■■■■■■■■
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引用次数: 0
Characteristics and outcomes of the Korean patients with coronavirus disease 2019; analyses of the national database 韩国2019冠状病毒病患者特征及转归分析对国家数据库的分析
IF 0.2 Pub Date : 2021-01-01 DOI: 10.4168/aard.2021.9.3.113
Sang-Heon Kim
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引用次数: 0
The impact of air pollution on allergic rhinitis 空气污染对变应性鼻炎的影响
IF 0.2 Pub Date : 2021-01-01 DOI: 10.4168/aard.2021.9.1.3
Ki-Il Lee, Young-Jun Chung, J. Mo
• This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT & Future Planning (2019R1F1A1060589) and funded by the Ministry of Education (2018R1D1A3B07048683). Received: November 27, 2020 Revised: December 21, 2020 Accepted: December 21, 2020 © 2021 The Korean Academy of Pediatric Allergy and Respiratory Disease The Korean Academy of Asthma, Allergy and Clinical Immunology This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/). 대기오염이 알레르기비염에 미치는 영향
•本研究由韩国科学、信息通信技术与未来规划部(2019R1F1A1060589)和教育部(2018R1D1A3B07048683)资助的韩国国家研究基金(NRF)基础科学研究计划支持。收稿日期:2020年11月27日修订日期:2020年12月21日接受日期:2020年12月21日©2021 The Korean Academy of Pediatric Allergy and Respiratory Disease The Korean Academy of Asthma, Allergy and Clinical Immunology这是一篇基于知识共享署名非商业许可(https://creativecommons.org/licenses/by-nc/4.0/)的开放获取文章。大黄蜂:大黄蜂:大黄蜂
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引用次数: 0
Analysis of PC20-FEF25%–75% and ΔFVC in the methacholine bronchial provocation test pc20 - fef25 ~ 75%及ΔFVC在甲胆碱支气管激发试验中的分析
IF 0.2 Pub Date : 2021-01-01 DOI: 10.4168/aard.2021.9.3.141
Hyeon A Kim, J. Kwon, J. Ahn, J. Choe, Dong Sub Kim, S. Park, M. Hyun, B. Choi
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引用次数: 0
Hypereosinophilia secondary to Sézary syndrome ssamzary综合征继发嗜酸性细胞增多症
IF 0.2 Pub Date : 2021-01-01 DOI: 10.4168/aard.2021.9.2.93
Y. Lee, Gyeongah Sim, Byung-Su Kim, Jungwon Hyun, Hyunchul Kim, Moon Seong Baek, Cheol-Hong Kim, I. Hyun, Jeong-Hee Choi
The Sézary syndrome is a leukemic form of cutaneous T-cell lymphoma characterized by the presence of erythroderma covering at least 80% of the body-surface area, lymphadenopathy, and the presence of clonally related neoplastic T cells with cerebriform nuclei (Sézary cells) in the blood, skin, and lymph nodes. Hypereosinophilia can be caused by hematologic malignancy with clonal abnor-mality, which is often associated with Sézary syndrome. Sézary syndrome has rarely been reported in Korea. However, hypereosinophilia in the Sézary syndrome has not been reported in Korea. Here, we report a case of 75-year-old man with hypereosinophila, erythroderma, and cutaneous T-cell lymphoma which was finally diagnosed as Sézary syndrome. ( Allergy Asthma Respir Dis 2021;9:93-98 )
ssamzary综合征是一种皮肤T细胞淋巴瘤的白血病形式,其特征是红皮病覆盖至少80%的体表面积,淋巴结病变,以及血液、皮肤和淋巴结中存在具有脑状核的克隆相关肿瘤T细胞(ssamzary细胞)。嗜酸性粒细胞增多症可由血液学恶性肿瘤与克隆异常引起,这通常与ssamzary综合征有关。ssamzary综合征在韩国很少有报道。然而,在韩国,ssamzary综合征中嗜酸性细胞增多症尚未报道。在此,我们报告一位75岁男性,患有嗜酸性粒细胞增多、红皮病和皮肤t细胞淋巴瘤,最后被诊断为ssamzary综合征。(过敏哮喘呼吸疾病2021;9:93-98)
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引用次数: 0
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Allergy, Asthma & Respiratory Disease
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