尼日利亚北部一名妇女自身免疫性肝炎

M. Manko, A. Jabir, Ahmadu Bello, A. Liman, S. Mustapha
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引用次数: 1

摘要

自身免疫性肝炎是一种病因不明的肝脏持续炎症。这是一种相对罕见的疾病,通常影响妇女,主要表现为慢性肝炎。它基本上分为1型和2型。患者是一名56岁的尼日利亚北部妇女,有甲状腺疾病和类风湿关节炎的背景,表现为黄疸和疲劳,肝酶升高,血清总蛋白升高,血清白蛋白低。进一步评估显示无反应性乙型肝炎和丙型肝炎标志物,腹部超声扫描慢性肝病特征,抗核和抗平滑肌抗体升高,血清IgG升高。肝脏组织学表现为慢性肝炎特征,符合AIH。最终诊断为AIH 1型,患者开始强的松龙联合硫唑嘌呤治疗,开始治疗几周后肝功能检查有所改善。据我们所知,尼日利亚仅报告了2例艾滋病病例,均来自尼日利亚南部的伊巴丹。尼日利亚北部没有艾滋病报告。因此,我们报告一例AIH 1型,以提高临床医生的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Autoimmune hepatitis in a Northern Nigerian woman
Autoimmune hepatitis is an unrelenting inflammation of the liver of unknown etiology. It is a relatively rare disease that commonly affects women and mostly present as chronic hepatitis. It is basically classified into types 1 and 2. The patient is a 56 year old Northern Nigerian woman with background thyroid disease and rheumatoid arthritis who presented with jaundice and fatigue and elevated liver enzymes with increased serum total protein and low serum albumin. Further evaluation showed non-reactive hepatitis B and C markers, features of chronic liver disease on abdominal ultrasound scanning, elevated anti-nuclear and anti-smooth muscle antibodies and increased serum IgG. Liver histology showed features of chronic hepatitis consistent with AIH. Diagnosis of AIH type 1 was eventually made and patient was started on prednisolone and azathioprine combination therapy with improvement of liver function test few weeks after commencement of therapy. To the best of our knowledge, only 2 cases of AIH has been reported in Nigeria, all from Ibadan, Southern Nigeria. No report of AIH from Northern Nigeria. We therefore report a case of AIH type 1 to increase awareness among clinicians.
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