Dourakis S P, Deutsch M, Hadziyannis S J
Academic Department of Medicine, Hippokration General Hospital, Athens, Greece.
J Hepatol. 1996 Dec;25(6):972-5. doi: 10.1016/s0168-8278(96)80304-7.
Thrombocytopenia is often found in patients with liver diseases, especially due to congestive splenomegaly caused by portal hypertension. Immune thrombocytopenia has been described rarely, and it seems to be especially associated with hepatitis C virus, which has been described as having a particular interaction with the immune system contributing to the induction of autoimmunity. Interferons, on the other hand, because of their immunomodulatory properties, are able to induce or exacerbate autoimmune diseases. Mild thrombocytopenia is a common adverse effect of interferon therapy. Severe life-threatening thrombocytopenia is extremely rare. We report two cases of severe immune thrombocytopenia in patients with chronic hepatitis C, probably induced by alpha-interferon. Bone marrow aspirate and elevated platelet-associated IgG antibodies, determined by indirect immunofluorescence, were suggestive of immune thrombocytopenia. None of the patients had any clinical sign of autoimmune syndrome, including arthritis, serositis, Sicca syndrome, vasculitis, thyroid abnormalities and others. Cryoglobulins and rheumatoid factor were tested and were undetectable. The patients' histories of exposure to alpha-interferon and the exclusion of other causes are most consistent with drug-induced immune thrombocytopenia. After alpha-interferon withdrawal, thrombocytopenia was treated successfully with prednisolone and immunoglobulins. Response to treatment was consistent with the diagnosis of alpha-interferon-induced immune thrombocytopenia and peripheral consumption of platelets.
血小板减少症在肝病患者中很常见,尤其是由门静脉高压引起的充血性脾肿大所致。免疫性血小板减少症很少被描述,似乎特别与丙型肝炎病毒有关,丙型肝炎病毒被认为与免疫系统有特殊相互作用,可导致自身免疫的诱导。另一方面,干扰素由于其免疫调节特性,能够诱导或加重自身免疫性疾病。轻度血小板减少症是干扰素治疗的常见不良反应。严重的危及生命的血小板减少症极为罕见。我们报告两例慢性丙型肝炎患者发生严重免疫性血小板减少症,可能由α干扰素诱导。骨髓穿刺以及通过间接免疫荧光法测定的血小板相关IgG抗体升高提示免疫性血小板减少症。患者均无自身免疫综合征的任何临床症状,包括关节炎、浆膜炎、干燥综合征、血管炎、甲状腺异常等。检测了冷球蛋白和类风湿因子,均未检测到。患者接触α干扰素的病史以及排除其他病因,与药物性免疫性血小板减少症最为相符。停用α干扰素后,血小板减少症用泼尼松龙和免疫球蛋白成功治疗。治疗反应与α干扰素诱导的免疫性血小板减少症及外周血小板消耗的诊断一致。