Sauter N P, Atkins M B, Mier J W, Lechan R M
Department of Medicine, New England Medical Center Hospitals, Boston, Massachusetts.
Am J Med. 1992 Apr;92(4):441-4. doi: 10.1016/0002-9343(92)90278-j.
A 59-year-old man with metastatic renal cell carcinoma developed symptomatic thyroid dysfunction following interleukin-2 (IL-2) and interferon-alpha (IFN-alpha) therapy. Thyroid evaluation prior to this therapy revealed evidence of subclinical Hashimoto's thyroiditis. Symptomatic thyrotoxicosis, including atrial fibrillation, developed after the initial two courses of intermittent intravenous bolus therapy with human recombinant IL-2 and IFN-alpha. At 4 weeks after initiation of immunotherapy, the thyroid antimicrosomal antibody (AMA) titer rose from 1:6,400 to 1:25,600; thyroid-stimulating immunoglobulin was negative. A technetium 99m-pertechnetate thyroid scan obtained while the patient was thyrotoxic showed diminished uptake in a symmetrically enlarged gland. The patient was temporarily treated with propranolol, digoxin, and quinidine. The atrial fibrillation quickly resolved, and thyrotoxicosis abated over the following 5 weeks, while the AMA titer rose further to 1:102,400. By 11 weeks after initiation of immunotherapy, hypothyroidism developed and persisted through two subsequent courses of cytokine therapy at Weeks 16 and 18. The tumor metastases partially responded to the immunotherapy. The patient has remained hypothyroid up to 27 weeks of follow-up. This case history suggests that IL-2 and IFN-alpha therapy may precipitate a fulminant autoimmune thyroiditis syndrome in a vulnerable patient with preexisting autoimmune thyroid disease.
一名59岁的转移性肾细胞癌男性患者在接受白细胞介素-2(IL-2)和α干扰素(IFN-α)治疗后出现了有症状的甲状腺功能障碍。在该治疗之前的甲状腺评估显示有亚临床桥本甲状腺炎的证据。在用重组人IL-2和IFN-α进行最初两个疗程的间歇性静脉推注治疗后,出现了包括心房颤动在内的有症状甲状腺毒症。在免疫治疗开始4周时,甲状腺微粒体抗体(AMA)滴度从1:6400升至1:25600;甲状腺刺激免疫球蛋白为阴性。在患者处于甲状腺毒症状态时进行的锝99m-高锝酸盐甲状腺扫描显示,对称增大的腺体摄取减少。患者接受了普萘洛尔、地高辛和奎尼丁的临时治疗。心房颤动迅速得到缓解,甲状腺毒症在接下来的5周内减轻,而AMA滴度进一步升至1:102400。在免疫治疗开始11周时,出现了甲状腺功能减退,并在第16周和第18周的后续两个疗程细胞因子治疗期间持续存在。肿瘤转移对免疫治疗有部分反应。在长达27周的随访中,患者一直处于甲状腺功能减退状态。该病例史表明,IL-2和IFN-α治疗可能在已有自身免疫性甲状腺疾病的易感患者中引发暴发性自身免疫性甲状腺炎综合征。