Severe Hepatocellular Injury With Transaminases > 20,000 IU/L in Suspected Repeated Drug Ingestion Despite Undetectable Serum Levels

Acetaminophen toxicity is a leading cause of acute liver injury and is typically evaluated using serum acetaminophen levels and the Rumack-Matthew nomogram. However, this approach does not apply to repeated supratherapeutic ingestion or delayed presentation, where levels may be low or undetectable despite severe liver injury. We report a 38-year-old woman with alcohol use disorder who presented with epigastric pain, nausea, and vomiting and was found to have acute-on-chronic pancreatitis and marked hepatocellular injury. Her liver enzymes rapidly worsened, peaking at aspartate transferase (AST) 22,966 IU/L and alanine aminotransferase (ALT) 1,498 IU/L, while the serum acetaminophen level remained <10 µg/mL. Further history revealed repeated ingestion of approximately 9 g of acetaminophen daily for four to five days prior to admission. Intravenous N-acetylcysteine was initiated despite the undetectable level. Liver enzymes subsequently improved, and the patient remained hemodynamically stable without encephalopathy. This case highlights that an undetectable acetaminophen level does not exclude severe toxicity and emphasizes the importance of early empiric treatment when clinical suspicion is high.

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Publication Details

Journal
Cureus
Published
2026-03-13
DOI
https://doi.org/10.7759/cureus.105189
Primary Topic
Drug-Induced Hepatotoxicity and Protection
Type
article
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article

Severe Hepatocellular Injury With Transaminases > 20,000 IU/L in Suspected Repeated Drug Ingestion Despite Undetectable Serum Levels

Ajantha Rangasamy, Rehan Shah, Rubba S Khan, Vismay Patel
Cureus
Drug-Induced Hepatotoxicity and Protection
article

Severe Hepatocellular Injury With Transaminases > 20,000 IU/L in Suspected Repeated Drug Ingestion Despite Undetectable Serum Levels

Ajantha Rangasamy, Rehan Shah, Rubba S Khan, Vismay Patel
article en

Abstract

Acetaminophen toxicity is a leading cause of acute liver injury and is typically evaluated using serum acetaminophen levels and the Rumack-Matthew nomogram. However, this approach does not apply to repeated supratherapeutic ingestion or delayed presentation, where levels may be low or undetectable despite severe liver injury. We report a 38-year-old woman with alcohol use disorder who presented with epigastric pain, nausea, and vomiting and was found to have acute-on-chronic pancreatitis and marked hepatocellular injury. Her liver enzymes rapidly worsened, peaking at aspartate transferase (AST) 22,966 IU/L and alanine aminotransferase (ALT) 1,498 IU/L, while the serum acetaminophen level remained <10 µg/mL. Further history revealed repeated ingestion of approximately 9 g of acetaminophen daily for four to five days prior to admission. Intravenous N-acetylcysteine was initiated despite the undetectable level. Liver enzymes subsequently improved, and the patient remained hemodynamically stable without encephalopathy. This case highlights that an undetectable acetaminophen level does not exclude severe toxicity and emphasizes the importance of early empiric treatment when clinical suspicion is high.

Cureus
Good health and well-being
Openalex Percentile: Top 20%
Drug-Induced Hepatotoxicity and Protection
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