Tanaka Y, Hayashida K, Ikematsu W, Umeno M, Ishibashi H, Niho Y
First Department of Internal Medicine, Faculty of Medicine, Kyushu University.
Nihon Rinsho Meneki Gakkai Kaishi. 1996 Apr;19(2):150-6. doi: 10.2177/jsci.19.150.
We herein report a case of chronic hepatitis C where the patient developed severe thrombocytopenia during interferon therapy. The patient was a 61-year-old woman, who received interferon therapy on April 27, 1993 under the diagnosis of C type chronic active hepatitis. After 4 weeks, her platelet count had decreased to 18,000/microliters and intraoral hemorrhage had begun. Although she received 250 mg of methylprednisolone and 20 U of platelet transfusion three times, her platelet count continued to decrease to 4,000/microliters on both May 28, and on June 3, 1993, and so she was transferred to our hospital on June 4. On her second admission to our hospital, although the platelet-associated IgG (PA-IgG) had increased markedly and the megakaryocytes in her bone marrow had decreased, her platelet count had already increased to 37,000/ microliters, and this gradually returned to a normal level accompanied with a decrease of PA-IgG within one month In this case, although we found immunological abnormalities (high level of IgG, positive ANA and positive anti-smooth muscle antibody) prior to interferon treatment, we could not diagnose the patient as having suffered from autoimmune disease, including autoimmune hepatitis, because she did not satisfy the necessary criteria and because she did not have any symptoms suggesting autoimmune disease. We consider that there may be the possibility that interferon induced only an anti-platelet antibodies that caused the high level of PA-IgG and decreased the production level of platelets within the bone marrow.
我们在此报告一例慢性丙型肝炎患者,该患者在干扰素治疗期间出现严重血小板减少。患者为一名61岁女性,于1993年4月27日因丙型慢性活动性肝炎诊断接受干扰素治疗。4周后,她的血小板计数降至18,000/微升,口腔内开始出血。尽管她三次接受了250毫克甲泼尼龙和20单位血小板输注,但其血小板计数在1993年5月28日和6月3日继续降至4,000/微升,因此于6月4日转至我院。在她第二次入住我院时,尽管血小板相关IgG(PA-IgG)显著升高且骨髓中的巨核细胞减少,但其血小板计数已升至37,000/微升,并在一个月内随着PA-IgG的降低逐渐恢复至正常水平。在该病例中,尽管我们在干扰素治疗前发现了免疫异常(IgG水平升高、ANA阳性和抗平滑肌抗体阳性),但由于她不符合必要标准且没有任何提示自身免疫性疾病的症状,我们无法将该患者诊断为患有自身免疫性疾病,包括自身免疫性肝炎。我们认为可能存在干扰素仅诱导抗血小板抗体的可能性,该抗体导致PA-IgG水平升高并降低了骨髓内血小板的生成水平。