Results 141 to 150 of about 16,016 (250)
Sepsis-Associated Cholestasis: The Impact of Mitochondrial Dysfunction (A Case Report)
, 2021 Behzad Noroozi +7 more
openalex +1 more source
Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Immune‐mediated hepatitis caused by immune checkpoint inhibitors (ICIs) is typically suspected based on aminotransferase elevation; however, biochemical signals may be blunted in advanced cirrhosis, potentially delaying recognition. A 71‐year‐old woman with cirrhosis due to metabolic dysfunction–associated steatohepatitis and Barcelona Clinic ...
Hidenobu Hara +17 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Autoimmune hepatitis is a type of chronic hepatitis that is usually progressive, has unknown etiology, and can occur at any age. In the present case, drug‐associated autoimmune hepatitis (DIAIH) was discussed, and DIAIH secondary to isoniazid (INH) was found in two case reports in the literature.
Murat AY, Erhan Bozkurt
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Delayed diagnosis invariably worsens outcomes in occult paraquat poisoning regardless of exposure route. Implement early urinary screening for suspected cases. Tailor antioxidant and anti‐fibrotic timing to toxicokinetic patterns to mitigate irreversible pulmonary damage.
Minhong Zhao +5 more
wiley +1 more source
The Role of Membrane Transport in Drug-Induced Hepatotoxicity and Cholestasis
, 2002 Peter L. M. Jansen, Michael Müller
openalex +2 more sources
Hepatic Sarcoidosis Unmasked by Chronic Pruritus and Esophageal Varices: A Case Report
Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Sarcoidosis is a granulomatous disease that affects multiple organs, commonly the liver, with manifestations from asymptomatic disease to cirrhosis and liver failure. A 43‐year‐old male presented with generalized pruritus. Liver biopsy demonstrated findings consistent with sarcoidosis, and treatment was initiated. We emphasize timely follow‐up
Ming Zheng +2 more
wiley +1 more source
Novel Variant ATP8B1 mutation in a child with progressive familial intrahepatic cholestasis (type 1)
, 2020 Nida Mirza +3 more
openalex +1 more source
Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Cholestasis beyond infancy is uncommon and presents a diagnostic challenge. We report an 11‐year‐old girl presenting with severe pruritus followed by jaundice and a cholestatic biochemical profile with normal gamma‐glutamyl transferase levels. Extensive evaluation excluded infectious, autoimmune, metabolic, and obstructive causes. Liver biopsy
Ahmad Hosiian +6 more
wiley +1 more source