نتایج جستجو برای: Congenital Hepatic Fibrosis

تعداد نتایج: 311139  

آنتیک چی, محمد حسین, حسینی, رویا السادات,

Congenital hepatic fibrosis (CHF) is a rare disease that primarily involves hepatobiliary and renal systems. It is characterized by hepatic fibrosis, portal hypertension and renal cystic disease. We present a 22 years old man with fever, abdominal pain, icterus and hematemesis. On complete work up of the patient and liver with kidney biopsy, the diagnosis was congenital hepatic fibrosis.

Journal: :acta medica iranica 0
fatemeh farahmand department of pediatric gastroenterology, pediatrics center of excellence, children's medical center, tehran university of medical sciences, tehran, iran. khadije soleimani department of cardiology, arak university of medical sciences, arak, iran. mojtaba hashemi department of cardiology, arak university of medical sciences, arak, iran. arezoo shafieyoun research center for immunodeficiencies, children's medical center, tehran university of medical sciences, tehran, iran. nima rezaei research center for immunodeficiencies, children's medical center, tehran university of medical sciences, tehran, iran. and molecular immunology research center, department of immunology, school of medicine, tehran university of medical sciences, tehran, iran. azizollah yousefi department of pediatric gastroenterology, pediatrics center of excellence, children's medical center, tehran university of medical sciences, tehran, iran.

congenital hepatic fibrosis (chf) is a developmental disorder of the biliary system, characterized by defective remodeling of the ductal plate. herein a family of three children, from consanguineous parents, with minor thalassemia is presented who suffered from congenital hepatic fibrosis (chf). prompt diagnosis and appropriate treatment are necessary to avoid further complications in the affec...

A Azarfar Ag Keykhosravi MA Kiani Y Ravanshad

Congenital Hepatic Fibrosis (CHF) is a rare disease that affects both the liver and kidneys.  Congenital hepatic fibrosis (CHF) is an autosomal recessive inherited malformation defined pathologically by a variable degree of periportal fibrosis and irregularly shaped proliferating bile ducts. Affected individuals also have impaired renal function, usually caused, in children and teenagers, by an...

Journal: :international journal of pediatrics 0
a azarfar assistant professor of pediatric nephrology, mashhad university of medical sciences, mashhad, iran. ma kiani associate professor of pediatric gastroentrology, mashhad university of medical sciences, mashhad, iran. ag keykhosravi associate professor of pediatric nephrology, mashhad university of medical sciences, mashhad, iran. y ravanshad 4mashhad university of medical sciences, mashhad, iran.

congenital hepatic fibrosis (chf) is a rare disease that affects both the liver and kidneys.  congenital hepatic fibrosis (chf) is an autosomal recessive inherited malformation defined pathologically by a variable degree of periportal fibrosis and irregularly shaped proliferating bile ducts. affected individuals also have impaired renal function, usually caused, in children and teenagers, by an...

A. R. Movassaghi, M. Rezaee Oghazi Z. Naseri

An aborted female Holstein foetus with marked generalized anasarca was referred to the Excellence Centre for Ruminant Abortion and Neonatal Mortality, Ferdowsi University of Mashhad. On postmortem examination, red-tinged ascites, pale and firm liver with extreme irregularity and numerous round to oval slightly raised foci on the capsular surface were seen. Histological examination revealed wide...

Journal: :iranian journal of veterinary research 2011
a. r. movassaghi z. naseri m. rezaee oghazi

an aborted female holstein foetus with marked generalized anasarca was referred to the excellence centre for ruminant abortion and neonatal mortality, ferdowsi university of mashhad. on postmortem examination, red-tinged ascites, pale and firm liver with extreme irregularity and numerous round to oval slightly raised foci on the capsular surface were seen. histological examination revealed wide...

Journal: :Gastroenterology 1965

میری علی‌آباد , قاسم , نوری , نورمحمد,

  Caroli’s disease is a rare congenital disorder characterized by multiple segmental cystic dilatations of the intra-hepatic bile ducts that are related to each other. Caroli’s syndrome is more common and associated with hepatic fibrosis and renal cystic disease. This paper introduces a three year old boy with Caroli’s disease and medullary nephrocalcinosis presented with fever, abdominal pain,...

2010
B. Geramizadeh P. Keramati A. Bahador H. Salahi S. Nikeghbalian S. M. Dehghani S. A. Malek-Hosseini

Herein, we describe two patients who underwent liver transplantation with the clinical diagnosis of hepatic failure and cryptogenic cirrhosis; histopathology of the explanted hepatectomy specimen revealed congenital hepatic fibrosis. To the best of our knowledge, coexistence of hepatic failure and cirrhosis in congenital hepatic fibrosis, have not yet been reported in the English literature.

2011
Mohammad Reza Ghadir Mohammad Bagheri Amir Hossein Ghanooni

INTRODUCTION Congenital hepatic fibrosis is an uncommon cause of portal hypertension. Despite the presence of portal hypertension, hepatocellular and renal function are usually well preserved. Congenital hepatic fibrosis is included in the group of congenital diseases of fibropolycystic disorders. These include a broad spectrum of clinical diseases which are usually accompanied by hepatic invol...

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