1.Drug-induced bile duct injury: progress and challenges.
Chinese Journal of Hepatology 2023;31(4):339-344
Drug-induced bile duct injury is a specific kind of drug-induced liver injury that has two main pathological types, namely ductopenia, or vanishing bile duct syndrome, and secondary sclerosing cholangitis. However, in recent years, the reports of new drugs that cause bile duct injury have been constantly increasing, and these drugs have different clinicopathological features and a novel pathogenesis. Therefore, this paper summarizes and analyzes the progress and challenges in the etiology, pathogenesis, diagnosis and treatment, and other aspects of drug-induced bile duct injury.
Humans
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Cholestasis/chemically induced*
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Cholangitis, Sclerosing/diagnosis*
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Chemical and Drug Induced Liver Injury/pathology*
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Bile Ducts/pathology*
2.A case of ticlopidine induced acute cholestatic hepatitis and pure red cell aplasia.
Ji Yeon LEE ; Eun Bum PARK ; Jae Hong AHN ; Sang Jun SUH ; Young Kul JUNG ; Ji Hoon KIM ; Bong Kyung SHIN ; Jin Hyuk YANG ; Jong Eun YEON ; Kwan Soo BYUN
The Korean Journal of Hepatology 2008;14(1):102-107
Ticlopidine inhibits platelet aggregation and provides beneficial secondary prevention of cerebrovascular and coronary artery disease. Frequently reported adverse effects of ticlopidine include diarrhea, nausea, and rash. However, to our knowledge, there are only a few published reports of the simultaneous occurrence of cholestatic hepatitis and pure red cell aplasia. Here we report a patient with simultaneous severe cholestatic hepatitis and pure red cell aplasia associated with ticlopidine. Although these adverse effects are rare, periodic hematological and liver function tests are recommended after starting ticlopidine.
Acute Disease
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Cholestasis/*chemically induced/diagnosis/etiology
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Female
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Hepatitis, Toxic/*diagnosis/pathology
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Humans
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Liver Function Tests
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Middle Aged
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Platelet Aggregation Inhibitors/*adverse effects
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Red-Cell Aplasia, Pure/*chemically induced/diagnosis/pathology
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Ticlopidine/*adverse effects
3.A case of allopurinol-induced granulomatous hepatitis with ductopenia and cholestasis.
Jae Young YOON ; Sun Yang MIN ; Ju Yee PARK ; Seung Goun HONG ; Sang Jong PARK ; So Ya PAIK ; Young Min PARK
The Korean Journal of Hepatology 2008;14(1):97-101
Allopurinol-induced hypersensitivity syndrome is characterized by an idiosyncratic reaction involving multiple-organs, which usually begins 2 to 6 weeks after starting allopurinol. In rare cases, the adverse reactions to allopurinol are accompanied by a variety of liver injury, such as reactive hepatitis, granulomatous hepatitis, vanishing bile duct syndrome, or fulminant hepatic failure. Here we report a case with granulomatous hepatitis and ductopenia. A 69-year-old man with chronic renal failure, hyperuricemia, and previously normal liver function presented with jaundice, skin rash, and fever 2 weeks after taking allopurinol (200 mg/day). In histopathology, a liver biopsy specimen showed mild spotty necrosis of hepatocytes, marked cholestasis in parenchyma, and some granulomas in the portal area. There were vacuolar degeneration in the interlobular bile ducts and ductopenia in the portal tracts. Pathologic criteria strongly suggested the presence of allopurinol-induced granulomatous hepatitis with ductopenia and cholestasis. The patient fully recovered following the early administration of systemic corticosteroid therapy.
Aged
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Allopurinol/*adverse effects/therapeutic use
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Antimetabolites/*adverse effects/therapeutic use
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Bile Duct Diseases/*chemically induced/diagnosis/pathology
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Bile Ducts, Intrahepatic/*drug effects/pathology
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Cholestasis/*chemically induced/diagnosis/pathology
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Drug Eruptions/pathology
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Granuloma/*chemically induced/pathology
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Hepatitis, Toxic/*pathology
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Humans
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Kidney Failure, Chronic/complications/drug therapy
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Male
4.Drug rash with eosinophilia and systemic symptoms syndrome following cholestatic hepatitis A: a case report.
Jihyun AN ; Joo Ho LEE ; Hyojeong LEE ; Eunsil YU ; Dan Bi LEE ; Ju Hyun SHIM ; Sunyoung YOON ; Yumi LEE ; Soeun PARK ; Han Chu LEE
The Korean Journal of Hepatology 2012;18(1):84-88
Hepatitis A virus (HAV) infections occur predominantly in children, and are usually self-limiting. However, 75-95% of the infections in adults are symptomatic (mostly with jaundice), with the illness symptoms usually persisting for a few weeks. Atypical manifestations include relapsing hepatitis, prolonged cholestasis, and complications involving renal injury. Drug rash with eosinophilia and systemic symptoms (DRESS) syndrome is a severe, drug-induced hypersensitivity reaction characterized by skin rash, fever, lymph-node enlargement, and internal organ involvement. We describe a 22-year-old male who presented with acute kidney injury and was diagnosed with prolonged cholestatic hepatitis A. The patient also developed DRESS syndrome due to antibiotic and/or antiviral treatment. To our knowledge, this is the first report of histopathologically confirmed DRESS syndrome due to antibiotic and/or antiviral treatment following HAV infection with cholestatic features and renal injury.
Acute Kidney Injury/diagnosis
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Anti-Bacterial Agents/*adverse effects/therapeutic use
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Cefotaxime/adverse effects/therapeutic use
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Cholestasis/complications/*diagnosis
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Cytomegalovirus/genetics
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Cytomegalovirus Infections/drug therapy/virology
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DNA, Viral/analysis
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Eosinophilia/etiology
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Exanthema/*chemically induced/pathology
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Ganciclovir/therapeutic use
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Hepatitis A/complications/*diagnosis/drug therapy
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Humans
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Hydrocortisone/therapeutic use
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Immunoglobulins/therapeutic use
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Male
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Syndrome
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Young Adult