Primary Biliary Cirrhosis Scenario of Libyan Patients in Tripoli University Hospital

Samira Alkuni Omar, Wael Ab A Diekna, Malak Mohamed Allafi, Firouz Torjman
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Abstract

Background and aims. Primary biliary cirrhosis (PBC) is an autoimmune, slowly progressive, cholestatic, liver disease characterized by a triad of chronic cholestasis, circulating anti-mitochondrial antibodies (AMA), and characteristic liver biopsy. A variant, called PBC-autoimmune hepatitis (AIH) overlap, is characterized by the above findings of PBC together with findings of elevated ALT, elevated Ig G, and ASMA. PBC is hypothesized to be related to environmental exposure in genetically vulnerable individuals. It typically occurs in middle-aged females. The aim of the current study is to describe the clinical and biochemical profile of adult Libyan Primary Biliary Cirrhotic patients. Method. This was a case series study conducted by reviewing the medical records of the 50 patients diagnosed as PBC and followed in gastro-enterology clinic in Tripoli university hospital during the study period. A relevant data obtained from the records in a preformed case sheet. Result. The total number of the diagnosed Primary Biliary Cirrhotic patients were 50 patients. All of them were females. Patient age during the study were from 35 to 65 years, about 90% of patients were symptomatic like gastrointestinal symptoms (jaundice in 100%, abdominal distention in 24%, and encephalopathy in 5 patients 10%), while, non- gastrointestinal symptoms like fatigue and weakness in 35 patients70%, skin disorders(pruritis) were diagnosed in 18 patients 36%), dyslipidemia in 15 patients 30%, and osteopenia in 7 patients 14%. Serological tests (AMA) was positive in ail patients and (ASMA) in 20% of patients, biochemical profile showed that Alkaline phosphatase was raised in all patients, while, 10 patients had raised AST and ALT 20%. Conclusion: middle-aged female patient with jaundice, fatigue and elevated alkaline phosphatase should be routinely undergoing serological testing (AMA) to check for primary biliary cirrhosis which should subsequently be verified by liver biopsy.
的黎波里大学医院利比亚患者原发性胆汁性肝硬化情况
背景和目的。原发性胆汁性肝硬化(PBC)是一种自身免疫性、缓慢进展、胆汁淤积的肝脏疾病,以慢性胆汁淤积、循环抗线粒体抗体(AMA)和特征性肝活检为特征。一种称为PBC-自身免疫性肝炎(AIH)重叠的变体,其特征是PBC的上述发现以及ALT升高、igg升高和ASMA。PBC被认为与遗传易感个体的环境暴露有关。它通常发生在中年女性身上。当前研究的目的是描述利比亚成人原发性胆汁性肝硬化患者的临床和生化特征。方法。这是一项病例系列研究,通过审查50名诊断为PBC的患者的医疗记录,并在研究期间在的黎波里大学医院的胃肠病学诊所进行随访。从预先编制的病例表的记录中获得的相关数据。结果。确诊原发性胆汁性肝硬化患者共50例。他们都是女性。研究期间患者年龄在35 - 65岁之间,约90%的患者有胃肠道症状(黄疸100%,腹胀24%,脑病5例,10%),非胃肠道症状如疲劳和虚弱35例(70%),皮肤病(瘙痒炎)18例(36%),血脂异常15例(30%),骨质减少7例(14%)。血清学试验(AMA)全部阳性,20%的患者ASMA阳性,生化分析显示所有患者碱性磷酸酶升高,10例患者AST和ALT升高20%。结论:中年女性黄疸、疲劳、碱性磷酸酶升高患者应常规行血清学检查(AMA),检查原发性胆汁性肝硬化,并行肝活检证实。
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