Recurrent intrahepatic cholestasis of pregnancy: Case report

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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...

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Severe First Trimester Recurrent Intrahepatic Cholestasis of Pregnancy: A Case Report and Literature Review

Background Intrahepatic cholestasis of pregnancy (ICP) is a disorder of defective bile acid transport that results in systemic accumulation of bile acids and typically presents in the third trimester of pregnancy with intense pruritus. A positive linear correlation exists between total bile acid level and poor pregnancy outcome, and labor is typically induced at 37 weeks gestation to prevent in...

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Severe 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 ...

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Intrahepatic 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...

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Progressive 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...

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ژورنال

عنوان ژورنال: The Journal of Kartal Training and Research Hospital

سال: 2011

ISSN: 1302-485X

DOI: 10.5505/jkartaltr.2011.82621