Garner Orlando, Ramirez-Berlioz Ana, Iardino Alfredo, Mocherla Satish, Bhairavarasu Kalpana
Department of Internal Medicine, Texas Tech University Health Sciences Center at The Permian Basin, Odessa, TX, USA.
Department of Infectious Disease, Midland Memorial Hospital, Midland, TX, USA.
Am J Case Rep. 2017 Dec 21;18:1365-1369. doi: 10.12659/ajcr.906391.
BACKGROUND Opportunistic infections may occur when patients with inflammatory bowel disease (IBD) are treated with tumor necrosis factor (TNF)-alpha inhibitors. With the increasing use of new immunosuppressant drugs, the incidence of opportunistic or atypical infections is also increasing, including with Nocardia spp. A high level of awareness of atypical infections is warranted in immunosuppressed patients. CASE REPORT A 57-year-old female African American, with a past medical history of ulcerative colitis (UC) and arthritis, was treated with infliximab and prednisone. She presented to the emergency department with acute onset of chest pain, shortness of breath, and a two-week history of a productive cough. Examination showed hypoxia, tachypnea, decreased and coarse bilateral breath sounds, and fluctuant, tender, erythematous masses on her trunk and groin. Laboratory investigations showed a leukocytosis with a left shift. She was initially treated for presumed community-acquired pneumonia (CAP). However, blood cultures grew Nocardia farcinica and treatment with trimethoprim-sulfamethoxazole (TMP-SMX) was begun, which was complicated by severe symptomatic hyponatremia. Following recovery from infection and resolution of the hyponatremia, the patient was discharged to a senior care facility, but with continued treatment with TMP-SMX. CONCLUSIONS To our knowledge, this is the first case of disseminated nocardiosis associated with infliximab treatment in a patient with ulcerative colitis. As with other forms of immunosuppressive therapy, patients who are treated with infliximab should be followed closely due to the increased risk of atypical infections. When initiating antibiotic therapy, careful monitoring of possible side effects should be done.
炎症性肠病(IBD)患者接受肿瘤坏死因子(TNF)-α抑制剂治疗时可能发生机会性感染。随着新型免疫抑制药物使用的增加,机会性或非典型感染的发生率也在上升,包括诺卡菌属感染。免疫抑制患者有必要高度警惕非典型感染。病例报告:一名57岁的非裔美国女性,有溃疡性结肠炎(UC)和关节炎病史,接受英夫利昔单抗和泼尼松治疗。她因突发胸痛、呼吸急促以及有两周的咳痰咳嗽史就诊于急诊科。检查发现有低氧血症、呼吸急促、双侧呼吸音减弱及粗糙,躯干和腹股沟有波动感、压痛性红斑肿块。实验室检查显示白细胞增多伴核左移。她最初被诊断为社区获得性肺炎(CAP)进行治疗。然而,血培养结果为鼻疽诺卡菌生长,遂开始使用复方磺胺甲恶唑(TMP-SMX)治疗,但出现了严重的症状性低钠血症并发症。感染治愈且低钠血症消退后,患者出院至老年护理机构,但继续接受TMP-SMX治疗。结论:据我们所知,这是首例溃疡性结肠炎患者因英夫利昔单抗治疗而发生播散性诺卡菌病。与其他形式的免疫抑制治疗一样,接受英夫利昔单抗治疗的患者因非典型感染风险增加,应密切随访。开始抗生素治疗时,应仔细监测可能出现的副作用。