美波利祖马布
苯拉唑马布
医学
恶化
嗜酸性
嗜酸性粒细胞增多症
鼻息肉
免疫学
中耳炎
鼻窦炎
哮喘
杜皮鲁玛
嗜酸性肺炎
白细胞介素5
过敏性支气管肺曲菌病
支气管肺泡灌洗
病理
胃肠病学
内科学
嗜酸性粒细胞
肺
白细胞介素
外科
免疫球蛋白E
细胞因子
抗体
作者
Hideyasu Shimizu,Masamichi Hayashi,Hisayuki Kato,Mayumi Nakagawa,Kazuyoshi Imaizumi,Mitsushi Okazawa
标识
DOI:10.3390/ijms222011209
摘要
A woman in her 50s was a super responder to benralizumab administered for the treatment of severe bronchial asthma (BA) with eosinophilic chronic rhinosinusitis with nasal polyp (ECRS) and eosinophilic otitis media (EOM). She exhibited the gradual exacerbation of ECRS/EOM despite good control of BA approximately 1 year after benralizumab initiation. Therefore, the treatment was switched to dupilumab, and the condition of the paranasal sinuses and middle ear greatly improved with the best control of her asthma. The patient reported that her physical condition was the best of her life. However, she developed a pulmonary opacity on chest computed tomography after 6 months. Histological examination of the lung parenchyma and cell differentiation of the bronchoalveolar lavage fluid indicated atypical chronic eosinophilic pneumonia, and treatment was switched to mepolizumab. Similarly to the period of benralizumab treatment, exacerbation of ECRS/EOM reduced her quality of life approximately 10 months after the administration of mepolizumab. Dupilumab was again introduced as a replacement for mepolizumab. The clinical course and consideration of the interaction between inflammatory cells led us to speculate that interleukin-13 could play a key role in the development of ECRS/EOM with severe BA.
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