Medical Oncology Department, Farhat Hached Hospital, Sousse 4011, Tunisia;
Pathology Department, Farhat Hached Hospital, Sousse 4011, Tunisia.
Cancer Biol Med. 2013 Sep;10(3):169-73. doi: 10.7497/j.issn.2095-3941.2013.03.008.
Autoimmune hepatitis (AIH) has rarely been described as an autoimmune paraneoplastic syndrome of thymoma. This case is the seventh case of AIH revealed by cholestasis few years after the diagnosis of thymoma and the first case treated with chemotherapy alone. We report in this paper a new approach to this rare severe condition. A 29 year-old man presented with chest pain and dyspnea with a history of thymoma surgically removed 4 years ago. CT scan showed the recurrence of an anterior mediastinal mass. Biology showed elevated liver enzymes and profound cholestasis. No sign of viral or toxic hepatitis or bile duct abnormalities were observed. Autoimmune antibodies, except for the anti-nuclear antibody, were negative. Liver biopsy showed active chronic AIH. The patient was diagnosed with recurrent thymoma with AIH and underwent 6 cycles of chemotherapy. A complete response on thymoma and cholestasis was obtained after 10 months of follow-up. Steroids and immunosuppressors are the standard treatment for AIH. The effect of chemotherapy as a specific treatment of this paraneoplastic syndrome needs to be considered.
自身免疫性肝炎(AIH)很少被描述为胸腺瘤的自身免疫性副肿瘤综合征。本病例为第七例在诊断为胸腺瘤数年后因胆汁淤积而引发的 AIH,也是首例单独接受化疗治疗的病例。本文报道了这一罕见严重疾病的新治疗方法。一名 29 岁男性,因胸痛和呼吸困难就诊,4 年前曾因胸腺瘤行手术切除。CT 扫描显示前纵隔肿块复发。生物学检查显示肝酶升高和严重的胆汁淤积。未观察到病毒性或中毒性肝炎或胆管异常的迹象。除抗核抗体外,自身免疫抗体均为阴性。肝活检显示活动性慢性 AIH。患者被诊断为复发性胸腺瘤合并 AIH,并接受了 6 个周期的化疗。在 10 个月的随访后,胸腺瘤和胆汁淤积完全缓解。皮质类固醇和免疫抑制剂是 AIH 的标准治疗方法。需要考虑化疗作为这种副肿瘤综合征的特定治疗方法的效果。