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Case Reports in Hepatology
ISSN 2090-6595 · Wiley · 69 artikel di indeks
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Artikel Jurnal
Prolonged Terlipressin Therapy as a Bridge to Curative TIPS for HRS–AKI in a Nontransplant Candidate
Hepatorenal syndrome–acute kidney injury (HRS–AKI) is a severe complication of advanced cirrhosis with high mortality and limited treatment options. Terlipressin is currently the only FDA-approved therapy for HRS, though recurrence is common upon discontinuation in patients without access to liver…
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Artikel Jurnal
Two Cases of Hepatic Epithelioid Hemangioendothelioma Misdiagnosed With Hepatic Veno-Occlusive Disease
Hepatic epithelioid hemangioendothelioma (HEHE) is a rare tumor of vascular origin with an incidence of
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Exceptionally Long Recurrence-Free Survival in a Male Patient With Fibrolamellar Hepatocellular Carcinoma
Fibrolamellar hepatocellular carcinoma (FLHCC) accounts for less than 1% of all primary liver cancers. Due to an absence of known risk factors, most individuals are diagnosed at advanced stages of disease. Subsequently, these tumors carry a 30%–50% mortality rate and a 33%–100% recurrence rate in…
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Artikel Jurnal
Vanishing Bile Duct Syndrome as an Uncommon Hepatic Paraneoplastic Syndrome in Hodgkin’s Lymphoma
Vanishing bile duct syndrome (VBDS) is a rare form of liver injury caused by ischemia, drug reactions, autoimmune diseases, infections, or malignancy. VBDS involves the progressive disappearance of intrahepatic bile ducts, causing cholestasis and biliary cirrhosis, with high mortality if untreated…
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Artikel Jurnal
Improvement in Irretractable Pruritus With Intrahepatic Portosystemic Shunt Embolization: From MAID to a New Lease on Life
Pruritus is a common, often debilitating symptom of liver disease. While most commonly seen in the setting of cholestasis and biliary obstruction, intrahepatic portosystemic shunts (PSSs) may also present with pruritus. The pathophysiology of intractable pruritus is not well understood and often…
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Transient Unexplained Severe Acute Hyperbilirubinaemia and Cholestasis in a Patient With Hereditary Spherocytosis
Hereditary spherocytosis is an inherited red cell membrane disorder resulting in haemolytic anaemia. Recognised clinical manifestations include anaemia, jaundice, splenomegaly and gallstones. Here we describe the case of a 40-year-old male with hereditary spherocytosis presenting with severe…
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Acute Liver Failure in an Adolescent Following Use of the Synthetic REV-ERB Agonist SR9009
Drug-induced liver injury (DILI) is a leading cause of acute liver failure (ALF) and an increasingly recognised consequence of unregulated performance-enhancing supplements. We report a 17-year-old male who presented with progressive jaundice and rapidly evolving ALF temporally associated with…
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Ashwagandha-Induced Herb-Induced Liver Injury Assessed With the Updated 2016 RUCAM
Ashwagandha-induced herb-induced liver injury (HILI) has increasingly been reported; however, many published cases show methodological variability in causality assessment and limited clinicopathological correlation. We present a case of ashwagandha-associated liver injury with systematic causality…
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Limitations of MELD in Isolated Polycystic Liver Disease: Fatal Traumatic Cyst Rupture Complicated by Abdominal Compartment Syndrome
Isolated polycystic liver disease (PLD) is rare and may cause debilitating mass-effect symptoms despite relatively preserved hepatic synthetic function. Because the Model for End-Stage Liver Disease (MELD) score does not capture nutritional, functional, and mechanical disease burden, affected…
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An Unforeseen Diagnosis After Liver Transplantation for Acute Liver Failure: Extranodal NK/T-Cell Lymphoma
Acute liver failure (ALF) is a medical emergency characterized by hepatic encephalopathy in patients with recent-onset jaundice and coagulopathy. We present a case of a patient who developed ALF secondary to NK/T-cell lymphoma, with the diagnosis confirmed via histopathological analysis of the…
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A Case Report of Vanishing Bile Duct Syndrome Resulting From Thyroid Storm–Related Liver Injury and Postsurgical Biliary Tree Injury Overlap
This case involves a 46-year-old obese, prediabetic female with a complex medical history. It illustrates several diagnostic challenges, including differentiating between thyroid storm–related liver injury and underlying chronic liver disease. The gradual progression to a definitive diagnosis of…
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A Rare, Atypical Presentation of Decompensated Cirrhosis: Isolated Transudative Hepatic Chylothorax Without Ascites
Hepatic hydrothorax is an uncommon presentation of decompensated liver cirrhosis and usually presents after other complications of portal hypertension such as ascites. We report the case of a 73-year-old female with autoimmune hepatitis (AIH) treated with budesonide, presenting with a right-sided…
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Artikel Jurnal
Hepatic Peliosis due to Azathioprine in a Pediatric Kidney Transplant Recipient
Azathioprine, an antimetabolite drug interfering with purines synthesis, is one of the immunosuppressive maintenance therapy used in solid organ transplant or dysimmune disease. We report the case of a 5-year-old-girl with Stage 5 chronic kidney disease, who developed hepatic peliosis due to…