Kim Guriel N, Ho Sam, Saulino David, Liu Xiuli
College of Public Health, University of Florida, Gainesville, FL 32610, USA.
Department of Pathology, Immunology, and Laboratory Medicine, College of Medicine, University of Florida, Gainesville, FL 32610, USA.
Gastroenterology Res. 2021 Apr;14(2):129-137. doi: 10.14740/gr1378. Epub 2021 Apr 21.
Hepatic steatosis is common in everyday liver pathology practice. There are many etiologies leading to hepatic steatosis. These etiologies include metabolic syndrome, alcohol, medications, monogenetic disease, infectious diseases, and malnutrition. Correct diagnosis of underlying etiology through clinicopathological correlation is key to adequate treatment and optimal outcome for the patient. In this case report, we describe severe protein-calorie malnutrition as an etiology for hepatic steatosis in a middle-aged woman who presented with lethargy, low body mass index (15.8 kg/m), abdominal distention and bilateral lower extremity edema, hyperammonemia, and hypoalbuminemia, 13 years after Roux-en-Y gastric bypass for morbid obesity. Laboratory tests revealed hyperammonemia, hypoalbuminemia, and low ceruloplasmin levels. Hemodynamic measurement demonstrated high hepatic venous pressure gradient of 12 mm Hg. Transjugular liver biopsy showed moderate macrovesicular steatosis, mild siderosis, and abundant lipofuscin but no evidence of fibrosis, cirrhosis, or steatohepatitis. This patient was treated with lactulose and enteral feeding, however, the patient died of progressive liver failure 3 weeks after admission. We also review relevant literature to help diagnose protein-calorie malnutrition (kwashiorkor) and hepatic steatosis as a possible late complication of Roux-en-Y gastric bypass. In patients with hepatic steatosis, encephalopathy, hyperammonemia and portal hypertension, malnutrition should be considered as an etiology and diagnosed with a synthesis of clinical, pathological, and laboratory information. Kwashiorkor is a severe disease and should be treated promptly as it may be fatal as in our case.
肝脂肪变性在日常肝脏病理实践中很常见。导致肝脂肪变性的病因众多,包括代谢综合征、酒精、药物、单基因疾病、传染病和营养不良。通过临床病理相关性正确诊断潜在病因是患者获得充分治疗和最佳预后的关键。在本病例报告中,我们描述了一名中年女性,她在接受Roux-en-Y胃旁路手术治疗病态肥胖13年后,出现嗜睡、低体重指数(15.8kg/m²)、腹胀、双侧下肢水肿、高氨血症和低白蛋白血症,严重蛋白质-热量营养不良是其肝脂肪变性的病因。实验室检查显示高氨血症、低白蛋白血症和低铜蓝蛋白水平。血流动力学测量显示肝静脉压力梯度高达12mmHg。经颈静脉肝活检显示中度大泡性脂肪变性、轻度含铁血黄素沉着和大量脂褐素,但无纤维化、肝硬化或脂肪性肝炎的证据。该患者接受了乳果糖和肠内营养治疗,然而,患者在入院3周后死于进行性肝衰竭。我们还回顾了相关文献,以帮助诊断蛋白质-热量营养不良(夸希奥科病)和肝脂肪变性,其可能是Roux-en-Y胃旁路手术的晚期并发症。对于患有肝脂肪变性、脑病、高氨血症和门静脉高压的患者,应考虑营养不良为病因,并综合临床、病理和实验室信息进行诊断。夸希奥科病是一种严重疾病,应及时治疗,因为它可能像我们的病例一样致命。