Autoimmune Hepatitis with Concomitant Idiopathic Thrombocytopenic Purpura Diagnosed by Transjugular Liver Biopsy.

Case Reports in Hepatology Pub Date : 2018-12-09 eCollection Date: 2018-01-01 DOI:10.1155/2018/5305691
Hiromi Fukuda, Kazuhide Takata, Takanori Kitaguchi, Ryo Yamauchi, Hideo Kunimoto, Takashi Tanaka, Keiji Yokoyama, Daisuke Morihara, Yasuaki Takeyama, Satoshi Shakado, Ai Mogi, Shinichi Kora, Kaori Koga, Morishige Takeshita, Kengo Yoshimitsu, Shotaro Sakisaka
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引用次数: 2

Abstract

Patients with autoimmune hepatitis (AIH) may sometimes have concomitant idiopathic thrombocytopenic purpura (ITP). Severe thrombocytopenia in ITP interferes with percutaneous liver biopsy for pathological diagnosis of AIH. Here, we report a case of AIH with ITP in a 63-year-old woman. The patient presented to our hospital with liver dysfunction and thrombocytopenia. For histological examination, transjugular liver biopsy (TJLB) was performed, leading to a diagnosis of AIH. Corticosteroids treatment led to an improvement in her liver enzyme levels and platelet count. In conclusion, patients with AIH may sometimes have concomitant ITP. TJLB was effective for making the diagnosis of AIH with severe thrombocytopenia due to ITP.

Abstract Image

Abstract Image

Abstract Image

经颈静脉肝活检诊断自身免疫性肝炎合并特发性血小板减少性紫癜。
自身免疫性肝炎(AIH)患者有时可能伴有特发性血小板减少性紫癜(ITP)。ITP中严重的血小板减少干扰经皮肝活检对AIH的病理诊断。在这里,我们报告一例AIH合并ITP的63岁女性。患者以肝功能障碍和血小板减少症来我院就诊。组织学检查,经颈静脉肝活检(TJLB),导致AIH的诊断。皮质类固醇治疗改善了她的肝酶水平和血小板计数。总之,AIH患者有时可能伴有ITP。TJLB对ITP所致AIH合并严重血小板减少症的诊断是有效的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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