January 2011
Nobel Medicus Journal;Jan-Apr2011, Vol. 7 Issue 1, p106
Academic Journal
No abstract available.


Related Articles

  • Incidence of Gallstones in Liver Cirrhosis. Acalovschi, Monica; Badea, Radu; Pascu, Maria // American Journal of Gastroenterology;Sep1991, Vol. 86 Issue 9, p1179 

    We conducted a longitudinal follow-up of 72 patients with liver cirrhosis (LC) in order to assess gallstone (GS) incidence. The period of survey was 24.5 ± 12.2 months. Patients were divided into two groups: group I--26 patients with ascites at the start or appearing during follow-up, and...

  • Human herpesvirus type 8 in patients with cirrhosis independent of thrombocytopenia.  // Journal of Clinical Pathology;Mar2010, Vol. 63 Issue 3, p254 

    This article presents a study on the status of HHV-8 antibody and DNA in cirrhotic ascites compared to that in cirrhotic plasma. The study concludes that the seropositive rate for HHV-8 antibody in patients with cirrhosis is independent of thrombocytopenia. It also shows that the positive rate...

  • The Utility of Evaluating Low Serum Albumin Gradient Ascites in Patients With Cirrhosis. Khandwalla, Hashim E.; Fasakin, Yemi; El-Serag, Hashem B. // American Journal of Gastroenterology;Jun2009, Vol. 104 Issue 6, p1401 

    OBJECTIVES:Serum-ascites albumin gradient (SAAG) has been used extensively in the diagnostic workup of patients with ascites. A SAAG level of <1.1 g/dl is usually thought of as a result of nonportal hypertension etiologies, including malignancies, tuberculous peritonitis, and nephrotic syndrome....

  • Gaucher disease: New developments in treatment and etiology. Harmanci, Ozgur; Bayraktar, Yusuf; Wu, George Y. // World Journal of Gastroenterology;7/7/2008, Vol. 14 Issue 25, p3968 

    Gaucher disease (GD) is an autosomal recessive disease which if undiagnosed or diagnosed late results in devastating complications. Because of the heterozygous nature of GD, there is a wide spectrum of clinical presentation. Clinicians should be aware of this rare but potentially treatable...

  • Incidental Chylous Ascites at the Time of Cesarean Section. Thompson, Kida A.; Al Khabbaz, Antoun // Case Reports in Obstetrics & Gynecology;6/15/2015, Vol. 2015, p1 

    Chylous ascites has multiple etiologies including malignancies, liver cirrhosis, intraperitoneal infections, and trauma. It is rarely reported in pregnancy. We report a case of chylous ascites noted at the time of cesarean section performed at 35 weeks of gestation on a patient with preeclampsia...

  • New proposal for the serum ascites albumin gradient cut-off value in Chinese ascitic patients. Cai-feng Jiang; Bin Shi; Jian Shi; Zong-li Yuan; Wei-fen Xie // Diagnostic Pathology;2013, Vol. 8 Issue 1, p1 

    Background: Serum ascites albumin gradient (SAAG) has been recognized as a reliable marker in the differential diagnosis of ascites. The etiological background of cirrhosis is rather different between western countries and eastern countries. The threshold of SAAG in Chinese ascitic patients has...

  • Umbilical hernia repair in the presence of cirrhosis and ascites: results of a survey and review of the literature. McKay, A.; Dixon, E.; Bathe, O.; Sutherland, F. // Hernia;Oct2009, Vol. 13 Issue 5, p461 

    Umbilical hernias are common in cirrhotics, yet, their management poses several challenges. The objective of this paper was to evaluate the indications, selection criteria, and technical aspects of umbilical hernia repair in patients with cirrhosis and ascites. An extensive review of the...

  • ascites. Peters, Michael // BMA A-Z Family Medical Encyclopedia;2004, p72 

    An encyclopedia entry for "ascites" is presented. It refers to excess fluid in the peritoneal cavity. This entry notes the occurrence of ascites in any condition that causes generalized edema, such as in congestive heart failure, nephrotic syndrome and cirrhosis of the liver. Symptoms of ascites...

  • Environmental agents involved in the cause of primary biliary cirrhosis. McNally, Richard J.Q.; Kouroumalis, Elias // Disease Markers;2010, Vol. 29 Issue 6, p329 

    Primary biliary cirrhosis (PBC) is an immune mediated chronic cholestatic liver disease with a slowly progressive course It is a universal disease with a reported latitudinal gradient in prevalence and incidence. The aetiology of primary biliary cirrhosis is still unknown. It is characterized by...


Read the Article


Sorry, but this item is not currently available from your library.

Try another library?
Sign out of this library

Other Topics