Manivannan Ahila, Husain Sanam, Shukr Batool
Internal Medicine, Henry Ford Health System, Detroit, USA.
Pathology, Henry Ford Health System, Detroit, USA.
Cureus. 2023 May 19;15(5):e39247. doi: 10.7759/cureus.39247. eCollection 2023 May.
Wilson disease (WD) is an autosomal recessive genetic disorder caused by mutations of ATP7B, a copper transporter, which results in impaired copper clearance. Its clinical manifestations are varied and can result in a mix of hepatic and neuropsychiatric symptoms. We present the case of a 26-year-old female with a past medical history of alcohol use who presented with right upper quadrant abdominal pain with associated vomiting, jaundice, and fatigue. She was found to have signs and symptoms of decompensated cirrhosis and was initially concerned about superimposed alcoholic hepatitis. With low ceruloplasmin and alkaline phosphatase, the suspicion for WD remained, and the patient underwent liver transplantation due to her worsening clinical status. The quantitative hepatic copper content of the explanted liver was elevated, and genetic testing confirmed the diagnosis of WD. Our case highlights the importance of including WD in the differential of a young patient with severe liver disease, and it highlights the utility of the phosphatidyl ethanol (PEth) test as a marker for chronic severe alcohol use. In patients with a significant alcohol use history, the diagnosis of WD should still be considered for those with reasonable clinical suspicion.
威尔逊病(WD)是一种常染色体隐性遗传疾病,由铜转运蛋白ATP7B的突变引起,导致铜清除受损。其临床表现多样,可导致肝脏和神经精神症状的混合出现。我们报告一例26岁有饮酒史的女性患者,她出现右上腹腹痛并伴有呕吐、黄疸和疲劳。她被发现有失代偿性肝硬化的体征和症状,最初担心并发酒精性肝炎。由于血浆铜蓝蛋白和碱性磷酸酶水平较低,仍怀疑为WD,且患者因临床状况恶化接受了肝移植。移植肝脏的肝铜定量含量升高,基因检测确诊为WD。我们的病例强调了在患有严重肝病的年轻患者鉴别诊断中纳入WD的重要性,并且强调了磷脂酰乙醇(PEth)检测作为慢性重度饮酒标志物的实用性。在有大量饮酒史的患者中,对于有合理临床怀疑的患者仍应考虑WD的诊断。