Pieterse Elmar, van Ingen Jakko, van der Meijden Wilbert
Department of Nephrology, Radboudumc, Nijmegen, The Netherlands.
Department of Medical Microbiology, Radboudumc, Nijmegen, The Netherlands.
Kidney Med. 2024 Aug 14;6(10):100891. doi: 10.1016/j.xkme.2024.100891. eCollection 2024 Oct.
Immunosuppressive therapy after kidney transplantation is associated with an increased risk for the development of opportunistic infections, such as pneumonia (PJP). Belatacept, a selective costimulatory blocker that prevents T cell activation, was previously suggested to be a potential risk factor for PJP development in kidney transplant recipients. We present 2 cases of kidney transplant patients with PJP discovered unexpectedly during a diagnostic work-up for fever of unknown origin. Both patients lacked typical clinical findings such as hypoxia, ground-glass pattern on computed tomography, or suggestive biochemical alterations such as high lactate dehydrogenase levels or hypercalcemia. PJP should therefore be included in the differential diagnosis when evaluating fever in kidney transplant recipients receiving belatacept, even in the absence of typical pulmonary and laboratory findings.
肾移植后的免疫抑制治疗与机会性感染(如肺炎,卡氏肺孢子虫肺炎)的发生风险增加相关。贝拉西普是一种选择性共刺激阻滞剂,可防止T细胞活化,此前曾被认为是肾移植受者发生卡氏肺孢子虫肺炎的潜在危险因素。我们报告2例肾移植患者,在对不明原因发热进行诊断性检查时意外发现患有卡氏肺孢子虫肺炎。两名患者均缺乏典型的临床症状,如缺氧、计算机断层扫描上的磨玻璃影,或提示性的生化改变,如高乳酸脱氢酶水平或高钙血症。因此,在评估接受贝拉西普治疗的肾移植受者的发热情况时,即使没有典型的肺部和实验室检查结果,也应将卡氏肺孢子虫肺炎纳入鉴别诊断。