Case Report: Intrahepatic Cholestasis of Pregnancy
نویسندگان
چکیده
منابع مشابه
Recurrent intrahepatic cholestasis of pregnancy. A case report.
Intrahepatic cholestasis of pregnancy (ICP) represents a rare but severe pathology with serious consequences on the outcome of pregnancy. We present the cases of two sisters that came to our clinic with ICP in successive pregnancies. The fetus from a pregnancy with cholestasis can be affected by preterm birth, respiratory distress syndrome, intrauterine death in the third trimester and a possib...
متن کاملSevere intrahepatic cholestasis in pregnancy – case report and literature review
Intrahepatic cholestasis of pregnancy (ICP), a common hepatic disease in pregnancy, sometimes can result in adverse fetal outcome. We present the case of 37-year old woman in 34 gestational week of her second pregnancy with ICP, schizophrenia and anaemia. The patient was admitted to hospital with the worsening pruritus of palm and feet since 3 weeks. Current pregnancy also was complicated with ...
متن کاملIntrahepatic cholestasis of pregnancy.
Intrahepatic cholestasis of pregnancy is the most common pregnancy-specific liver disease that typically presents in the third trimester. The clinical features are maternal pruritus in the absence of a rash and deranged liver function tests, including raised serum bile acids. Intrahepatic cholestasis of pregnancy is associated with an increased risk of adverse perinatal outcomes, including spon...
متن کاملProgressive intrahepatic cholestasis (Byler's disease): case report.
This paper reports the case of a child in which the clinical and laboratory data indicate a progressive intrahepatic cholestasis of the type described as Byler's disease. The histological and histochemical findings suggest an intrahepatic cholestasis. Electron microscopy reveals interruptions of the bile canalicular membrane, which have been described as characteristic of this disease. A stri...
متن کاملProgressive Familial Intrahepatic Cholestasis - A Case Report
Introduction Progressive familial intrahepatic cholestasis (PFIC) represents a group of disorders which usually begin in the first months of life and progress to cirrhosis before the end of second decade. The disease occurs due to a defect in bile acid transport leading to cholestasis and resultant hepatocelluler injury1-3. Recent molecular and genetic studies have identified genes responsible ...
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ژورنال
عنوان ژورنال: Journal of Health and Allied Sciences NU
سال: 2016
ISSN: 2582-4287,2582-4953
DOI: 10.1055/s-0040-1709898