Severe cholestatic jaundice associated with Graves’ disease

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A case of severe cholestatic jaundice associated with Graves' disease.

Physical examination revealed severe jaundice. There were no signs of chronic liver disease. He was afebrile with a regular pulse rate of 100 beats per minute and normal blood pressure. He had no signs of thyroid eye disease and no external goiter. Respiratory and cardiovascular examinations were normal. Chest radiography and echocardiography excluded any kinds of cardiac failure. There was no ...

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Primary amyloidosis and severe intrahepatic cholestatic jaundice.

Liver involvement in systemic amyloidosis is frequent but is rarely of clinical importance. Five patients with severe cholestatic jaundice are described and an additional 20 from published reports are reviewed. The most frequent presenting symptoms were lethargy and abdominal pain, which were present for a median of 11 months before the onset of jaundice. Hepatomegaly, usually marked, was prese...

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Severe cholestatic jaundice secondary to hyperthyroidism

Introduction: Hyperthyroidism is a known cause of nonspecific abnormalities in liver biochemitries; most commonly mild elevations in serum bilirubin and liver enzymes. Case Report: A case of severe cholestatic jaundice secondary to Grave’s disease. The patient is a 28­year­old African­American male who presented to the emergency room with chronic diarrhea, weight loss and jaundice. At presentat...

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Neonatal Graves’ Disease and Cholestatic Jaundice: Case Series and Review of the Literature

Cholestatic jaundice and elevated liver enzymes are uncommon, but recognized, manifestations of neonatal thyrotoxicosis. Current guidelines for evaluation of cholestatic jaundice and reviews in Neonatology literature do not discuss hyperthyroidism in the differential diagnosis of cholestatic jaundice. We report two cases of neonatal thyrotoxicosis secondary to neonatal Graves’ disease that pres...

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Familial Intrahepatic Cholestatic Jaundice

Recurrent jaundice due to intrahepatic cholestasis is reported most often in adults. Some varieties are familial and are associated with failure of excretion of conjugated bilirubin by the liver cell. The original descriptions of these types given by Rotor, Manahan, and Florentin (1948) and Dubin and Johnson (1954) concerned patients with a benign recurrent jaundice. The diseases described by t...

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ژورنال

عنوان ژورنال: Clinical Case Reports

سال: 2018

ISSN: 2050-0904

DOI: 10.1002/ccr3.1859