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1.
Rom J Intern Med ; 50(1): 19-25, 2012.
Article in English | MEDLINE | ID: mdl-22788090

ABSTRACT

Even if the fatty liver is an entity recognized long time ago, only recently the non-alcoholic liver disease (NAFLD) came in attention. The fact that NAFLD might progress from simple steatosis to steatohepatitis and cirrhosis showed that NAFLD is not always a benign disorder. NAFLD has many etiological factors, but the majority of cases are those in the context of metabolic syndrome, known as primary NAFLD. Statins are well known as 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) inhibitors, but this class has also pleiotropic actions non-related with HMG-CoA inhibition. Particularly, the possible anti-inflammatory and anti-fibrinogenesis qualities make statins an option in NAFLD. So, regarding the statins treatment in NAFLD, there are two aspects that are important. First of all, if statins (that are essential in the therapy for the improvement of cardiovascular risk) are safe at patients with NAFLD, given their adverse effect of increasing hepatic transaminases. Secondly, considering the strong associations between NAFLD and metabolic syndrome components, like obesity and insulin resistance, if statins could be a therapeutic option for the patients with NAFLD in the absence of dyslipidemia.


Subject(s)
Fatty Liver/drug therapy , Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use , Disease Progression , Dose-Response Relationship, Drug , Fatty Liver/enzymology , Humans , Hydroxymethylglutaryl-CoA Reductase Inhibitors/administration & dosage , Non-alcoholic Fatty Liver Disease
2.
Chirurgia (Bucur) ; 99(4): 247-53, 2004.
Article in Romanian | MEDLINE | ID: mdl-15560562

ABSTRACT

This article presents a case of acute intermittent porphyria admitted to the Surgery Department of C.F. Craiova Hospital between 18.08.2003-26.08.2003 then transferred to the Colentina Hospital in Bucharest for diagnosis confirmation and adequate treatment. The purpose of this paper is to bring attention on a rare metabolic inherited disease that, due to its non-specific and often noisy symptoms and limited possibilities of biochemical, enzymatic and genetic diagnosis, could generate potential serious confusions. The presentes case illustrates the fact that sometimes the acute attack may be mistaken for an acute surgical affection which requires an emergency operation with all the aggravating consequences and delay in the real diagnosis. About 1% of acute attacks of porphyria may be fatal. Only the drugs known as safe should be prescribed. Basic treatment consists in oral and intravenous glucose and hematin administration.


Subject(s)
Abdomen, Acute/diagnosis , Porphyria, Acute Intermittent/diagnosis , Abdomen, Acute/drug therapy , Diagnosis, Differential , Drug Therapy, Combination , Glucose/therapeutic use , Hemin/therapeutic use , Humans , Male , Middle Aged , Porphyria, Acute Intermittent/drug therapy , Treatment Outcome
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