Gîlcă Georgiana-Emmanuela, Diaconescu Smaranda, Bălan Gheorghe Gh, Timofte Oana, Ştefănescu Gabriela
Gastroenterology Department University Clinical Emergency Hospital "Sf. Spiridon" "Gr. T. Popa" University of Medicine and Pharmacy 5th Pediatric Clinic Emergency Hospital for Children "Sf. Maria," Iasi, Romania.
Medicine (Baltimore). 2017 Mar;96(10):e6156. doi: 10.1097/MD.0000000000006156.
Although immunomodulatory therapy has been clearly stated as an important landmark in treatment of ulcerative colitis, significantly improving the quality of life for patients with inflammatory bowel disease, there are several aspects to be considered regarding the possible side-effects of anti-TNF alpha agents. In spite of a good safety profile, biologic TNF antagonists may induce paradoxical inflammation, which can manifest as sarcoid-like granulomatosis, consisting of noncaseating granulomas in the affected organs.
We report the case of a 30-year-old male patient, with no personal or familial history of lung disease, with a personal history of ulcerative colitis (UC), under clinical remission following infliximab therapy in maintenance dose, who was admitted for treatment administration, but also for dyspnea, nocturnal sweating, and nonproductive cough.
Based on clinical manifestations, biological landmarks excluding various infections, CT scan, fibrobronchoscopy with bronchoalveolar lavage for culture and immunohistochemical examination, followed by mediastinoscopy with sampling of paratracheal lymph node, which underwent histopathological examination, the patient was diagnosed with drug- induced stage II pulmonary sarcoidosis.
Since the patient had developed severe allergic reaction after being administered Infliximab at admission, the biological treatment was immediately discontinued. Following the diagnosis of pulmonary sarcoidosis, corticotherapy was initiated.
After corticotherapy was initiated, the patient had a favorable outcome at 3 months reevaluation, both regarding the course of ulcerative colitis and sarcoidosis.
Patients under biological therapy using anti-TNF alpha agents must be carefully monitored, in order to early identify potential paradoxical inflammation (such as sarcoidosis) as a side-effect. The drug-related pulmonary disease tends to improve upon withdrawal of the drug, with occasional requirement of steroid treatment. However, a thorough strategy should be assembled in the case of UC relapse in this patient category, with switching to adalimumab or surgical approach as main possibilities.
尽管免疫调节疗法已被明确视为治疗溃疡性结肠炎的一个重要里程碑,显著改善了炎症性肠病患者的生活质量,但对于抗TNFα药物可能产生的副作用仍有几个方面需要考虑。尽管生物TNF拮抗剂具有良好的安全性,但仍可能诱发反常性炎症,表现为结节病样肉芽肿病,在受影响器官中由非干酪样肉芽肿组成。
我们报告了一名30岁男性患者的病例,他无肺部疾病的个人或家族史,有溃疡性结肠炎(UC)病史,在维持剂量的英夫利昔单抗治疗后处于临床缓解期,因接受治疗而入院,同时伴有呼吸困难、夜间盗汗和干咳。
根据临床表现、排除各种感染的生物学指标、CT扫描、经纤维支气管镜进行支气管肺泡灌洗以进行培养和免疫组化检查,随后进行纵隔镜检查并取气管旁淋巴结样本进行组织病理学检查,该患者被诊断为药物性II期肺结节病。
由于患者入院时使用英夫利昔单抗后出现严重过敏反应,立即停止生物治疗。在诊断为肺结节病后,开始进行皮质激素治疗。
开始皮质激素治疗后,在3个月的复查中,患者在溃疡性结肠炎和结节病的病程方面均取得了良好的预后。
使用抗TNFα药物进行生物治疗的患者必须进行仔细监测,以便早期识别潜在的反常性炎症(如结节病)作为副作用。药物相关的肺部疾病在停药后往往会改善,偶尔需要进行类固醇治疗。然而,对于这类患者中UC复发的情况,应制定全面的策略,主要可能的选择是改用阿达木单抗或采取手术方法。