Department of Medicine, Division of Pulmonary, Critical Care, and Sleep Medicine, University of Florida, Gainesville, FL, USA.
J Asthma. 2021 Dec;58(12):1670-1674. doi: 10.1080/02770903.2020.1827416. Epub 2020 Oct 6.
Ustekinumab-induced eosinophilic pneumonia is rare and to our knowledge, this is the fifth reported case of such an entity.
A 60-year-old female was admitted with worsening shortness of breath and a nonproductive cough for 4 months. Her past medical history was significant for Crohn's disease and psoriatic arthritis that was previously managed with adalimumab and switched to ustekinumab 2 months before symptoms. Initial diagnostic workup showed 10% peripheral eosinophilia and a CT chest showed numerous 5 mm nodules scattered throughout the lungs along with some peripheral reticulations. Her BAL fluid analysis showed abnormally high eosinophil count (67%), greatly limiting her potential diagnoses to eosinophilic pneumonia, EGPA, and tropical pulmonary eosinophilia (TPE). AEP typically causes more severe disease with a rapid onset, and there was low suspicion for TPE based on history, leaving EGPA and CEP. Based on her negative autoimmune serology, a negative biopsy of the nasal mucosa (no vasculitis/granulomata or eosinophils), and negative infectious workup, the patient was diagnosed with CEP secondary to ustekinumab and the drug was stopped. She was started on high dose prednisone and after a prolonged taper over 5 months, her symptoms and nodules and reticulations on her CT scan resolved.
This case exemplifies the importance of identifying drug-induced lung diseases which in many cases might not have a strong temporal association with the symptom onset. It also highlights that some drugs owing to their long elimination half-time can remain in the system for a prolonged period and continues to cause symptoms despite their cessation and require prolonged treatment and reassurance.
The association of eosinophilic pneumonia with ustekinumab, a drug used in the treatment of psoriasis and other autoimmune diseases, is rare and there is a paucity of literature regarding this association.
乌司奴单抗诱导的嗜酸性肺炎较为罕见,据我们所知,这是第五例此类病例报告。
一名 60 岁女性因呼吸困难加重和 4 个月无痰咳嗽而入院。她既往有克罗恩病和银屑病关节炎病史,曾接受阿达木单抗治疗,2 个月前改用乌司奴单抗。最初的诊断性检查显示外周血嗜酸性粒细胞计数为 10%,胸部 CT 显示肺部有许多 5mm 结节,伴有一些周围网状影。她的 BAL 液分析显示异常高的嗜酸性粒细胞计数(67%),极大地限制了她的潜在诊断为嗜酸性肺炎、EGPA 和热带肺嗜酸性粒细胞增多症(TPE)。AEP 通常导致更严重的疾病,起病迅速,根据病史,TPE 的可能性较低,只剩下 EGPA 和 CEP。由于她自身免疫血清学阴性、鼻黏膜活检阴性(无血管炎/肉芽肿或嗜酸性粒细胞)以及阴性感染性检查,该患者被诊断为乌司奴单抗引起的 CEP,并停用该药。她开始接受大剂量泼尼松治疗,经过 5 个月的长时间减量后,她的症状、CT 扫描上的结节和网状影均得到缓解。
该病例说明了识别药物引起的肺部疾病的重要性,在许多情况下,这些疾病与症状发作之间可能没有很强的时间关联。它还强调了一些药物由于其长消除半衰期,可能在系统中停留很长时间,并在停药后继续引起症状,需要延长治疗和安抚。
乌司奴单抗(一种用于治疗银屑病和其他自身免疫性疾病的药物)与嗜酸性肺炎的关联较为罕见,关于这种关联的文献很少。