Almeida F, Amorim S, Sarmento A, Santos L
Infectious Diseases Department, Centro Hospitalar de São João, Porto, Portugal.
Cardiology Department, Centro Hospitalar de São João, Porto, Portugal.
Transplant Proc. 2018 Apr;50(3):933-938. doi: 10.1016/j.transproceed.2017.12.003. Epub 2018 Mar 24.
Noninfective pneumonitis is a class-related effect within mammalian target of rapamycin (mTOR) inhibitors, including everolimus, and can occasionally be severe.
A 62-year-old man, medicated with everolimus due to a heart transplantation 17 years previously and with chronic kidney disease, was admitted to the intensive care unit (ICU) with acute respiratory failure, cardiovascular shock, and impaired renal function requiring dialysis. Computed tomography (CT) scan revealed right upper lobe consolidation. Extensive microbiological workup, autoimmune testing, and cytology were negative and echocardiography showed preserved heart function. Everolimus levels were normal (5.7-6.1 ng/mL) and the drug was suspended at day 9. The patient was difficult to ventilate and responded poorly to broad-spectrum antibiotic and antifungal therapy. On day 25, CT scan and bronchoscopy revealed left-sided alveolar hemorrhage, and corticosteroid pulses were performed. The patient gradually improved. After discharge and 6 months of follow-up, clinical recovery was complete and chest imaging substantially improved.
Pneumonitis occurs in up to 4.3% of transplant recipients using everolimus for immunosuppression. Despite usually presenting as a mild and self-limited disease, severe cases have been described. Alveolar hemorrhage can occur and is associated with poor outcome. Everolimus levels do not seem to accurately predict toxicity. Corticosteroid therapy has been used with success in severe disease. We review the pathophysiological, clinical, and management-related aspects of this entity with emphasis on its potential severity.
Our case was a rare occurrence of severe life-threatening pulmonary disease related to everolimus. Awareness of the potential severity of this entity is important for the management of patients using mTOR inhibitors.
非感染性肺炎是哺乳动物雷帕霉素靶蛋白(mTOR)抑制剂(包括依维莫司)的一种类相关效应,偶尔可能较为严重。
一名62岁男性,17年前因心脏移植接受依维莫司治疗且患有慢性肾脏病,因急性呼吸衰竭、心血管休克和需要透析的肾功能损害入住重症监护病房(ICU)。计算机断层扫描(CT)显示右上叶实变。广泛的微生物学检查、自身免疫检测和细胞学检查均为阴性,超声心动图显示心脏功能正常。依维莫司水平正常(5.7 - 6.1 ng/mL),该药物在第9天停用。患者通气困难,对广谱抗生素和抗真菌治疗反应不佳。在第25天,CT扫描和支气管镜检查显示左侧肺泡出血,并进行了糖皮质激素冲击治疗。患者逐渐好转。出院后经6个月随访,临床完全康复,胸部影像学明显改善。
在使用依维莫司进行免疫抑制的移植受者中,肺炎发生率高达4.3%。尽管通常表现为轻度自限性疾病,但也有严重病例的报道。肺泡出血可能发生且与不良预后相关。依维莫司水平似乎不能准确预测毒性。糖皮质激素治疗在重症疾病中已成功应用。我们回顾了该疾病在病理生理、临床和管理方面的相关内容,重点关注其潜在的严重性。
我们的病例是与依维莫司相关的罕见严重危及生命的肺部疾病。认识到该疾病的潜在严重性对于使用mTOR抑制剂的患者管理很重要。