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自身免疫性肝炎合并免疫性血小板减少性紫癜

Autoimmune Hepatitis Associated with Immune Thrombocytopenic Purpura.

作者信息

Ito Akihiro, Yoshizawa Kaname, Fujimori Kazuya, Morita Susumu, Shigeno Takashi, Maejima Toshitaka

机构信息

Department of Gastroenterology, National Hospital Organization, Shinshu Ueda Medical Center, Japan.

出版信息

Intern Med. 2017;56(2):143-147. doi: 10.2169/internalmedicine.56.7506. Epub 2017 Jan 15.

Abstract

Although autoimmune hepatitis (AIH) is frequently complicated with chronic thyroiditis or other autoimmune disorders, reports on its association with immune thrombocytopenic purpura (ITP) are scarce. We herein describe a case of AIH associated with ITP. A 75-year-old Japanese woman was admitted to our hospital due to increased aminotransferase levels and severe thrombocytopenia. Elevated serum immunoglobulin G (IgG) was detected, and tests for platelet-associated IgG and anti-nuclear antibody were positive. Following the diagnosis of AIH-associated ITP, prednisolone treatment of 0.6 mg/kg/day resulted in a decrease in the aminotransferase levels and an increased platelet count.

摘要

虽然自身免疫性肝炎(AIH)常并发慢性甲状腺炎或其他自身免疫性疾病,但关于其与免疫性血小板减少性紫癜(ITP)关联的报道却很稀少。我们在此描述一例AIH合并ITP的病例。一名75岁的日本女性因转氨酶水平升高和严重血小板减少症入住我院。检测到血清免疫球蛋白G(IgG)升高,血小板相关IgG和抗核抗体检测呈阳性。在诊断为AIH相关ITP后,给予泼尼松龙0.6mg/kg/天的治疗使转氨酶水平下降,血小板计数增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886d/5337457/42d5e630b0a1/1349-7235-56-0143-g001.jpg

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