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自身免疫性肝炎伪装为铁过载综合征:尼日利亚男性的诊断困境。

Autoimmune Hepatitis Disguised as Iron Overload Syndrome: Diagnostic Dilemma in a Nigerian Man.

机构信息

Marshall University, Huntington, WV, USA.

Memorial Hospital Belleville, IL, USA.

出版信息

J Investig Med High Impact Case Rep. 2023 Jan-Dec;11:23247096231175442. doi: 10.1177/23247096231175442.

Abstract

Autoimmune hepatitis (AIH) is an extremely rare cause of chronic liver disease (CLD) in sub-Saharan Africa-there have only been 3 reported cases of AIH in Nigeria, a country of about 200 million people. We report the first case of AIH in a male patient in Nigeria and highlight its unusual presentation. A 41-year-old man with jaundice and malaise for 3 months was referred for evaluation after investigations revealed deranged liver enzymes and a cirrhotic liver. Laboratory evaluation revealed high serum immunoglobulin G, but there was also marked elevation of serum ferritin and transferrin saturation, resulting in a diagnostic dilemma between AIH and an iron overload condition such as hemochromatosis. A liver biopsy was crucial in providing a definitive diagnosis of AIH. Despite its rarity, clinicians should maintain a high index of suspicion for AIH in sub-Saharan Africa and should proceed to a liver biopsy when the cause of CLD is unclear.

摘要

自身免疫性肝炎(AIH)是撒哈拉以南非洲地区慢性肝病(CLD)的极罕见病因-在拥有约 2 亿人口的尼日利亚,仅有 3 例 AIH 报告病例。我们报告了尼日利亚首例 AIH 男性患者病例,并强调了其不常见的表现。一名 41 岁男性因黄疸和不适 3 个月而被转介进行评估,因为检查显示肝功能酶异常和肝硬化。实验室评估显示血清免疫球蛋白 G 升高,但血清铁蛋白和转铁蛋白饱和度也显著升高,导致在 AIH 和铁过载病症(如血色病)之间存在诊断难题。肝活检对于提供 AIH 的明确诊断至关重要。尽管其罕见,但在撒哈拉以南非洲地区,临床医生应保持对 AIH 的高度怀疑,并在 CLD 病因不明时进行肝活检。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc50/10204042/dcf7dbf27f36/10.1177_23247096231175442-fig1.jpg

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