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一名接受α干扰素治疗且获得完全基因缓解的慢性髓性白血病患者发生严重自身免疫性肝炎。

Severe autoimmune hepatitis in a chronic myeloid leukemia patient treated with interferon alpha and with complete genetic response.

作者信息

Steegmann J L, Requena M J, García-Buey M L, Granados E, Romero R, Fernández-Rañada J M, Moreno R

机构信息

Hematology Department, Hospital Universitario de la Princesa, Madrid, Spain.

出版信息

Am J Hematol. 1998 Sep;59(1):95-7. doi: 10.1002/(sici)1096-8652(199809)59:1<95::aid-ajh19>3.0.co;2-0.

Abstract

A patient with chronic myeloid leukemia (CML) treated with interferon alpha (IFN alpha) and who developed autoimmune hepatitis (AIH) is described. The patient was treated with IFN alpha 2a, a complete cytogenetic response was achieved 5 months later, and this response has lasted now more than 7 years. Autoimmune hypothyroidism appeared at 18 months of treatment, and 1 year later severe type I autoimmune hepatitis developed. To our knowledge this is the first report of such complication in an IFN alpha-treated CML patient.

摘要

本文描述了一名接受α干扰素(IFNα)治疗的慢性髓性白血病(CML)患者,该患者发生了自身免疫性肝炎(AIH)。该患者接受了IFNα 2a治疗,5个月后实现了完全细胞遗传学缓解,且这种缓解持续至今已超过7年。治疗18个月时出现自身免疫性甲状腺功能减退,1年后发生严重的I型自身免疫性肝炎。据我们所知,这是IFNα治疗的CML患者出现此类并发症的首例报告。

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