S5461 A Fatal Synergy: Acute Liver Failure From COVID-19 and Herbal Supplement With Undeclared Ingredients

Introduction: Drug-induced liver injury (DILI) and viral infections are important considerations in the broad differential diagnosis of hepatobiliary injury, particularly after the exclusion of more common etiologies. We present a fatal case of biopsy-proven acute liver failure from concurrent Coronavirus 2019 (COVID-19) infection and DILI due to Artri King, an over-the-counter herbal supplement containing undisclosed hepatotoxic ingredients. Case Description/Methods: A 56-year-old man with systemic lupus erythematosus presented with abdominal distension and jaundice. The patient reported increased consumption of Artri King for joint pain and denied additional home medications. Labs demonstrated elevated total bilirubin (7.2 mg/dL), severe transaminitis (alanine aminotransferase 2,909 IU/L), low fibrinogen, low platelets, elevated international normalized ratio of 2, EBV reactivation, and positive SARS CoV-2 PCR. Negative workup included: computed tomography of the abdomen, urine and serum toxicology, viral and autoimmune serology, and hereditary causes. Within 24 hours of admission, the patient started an N-acetyl cystine protocol. Despite improvement in transaminases, total bilirubin continued to rise to 30.3 mg/dL prompting liver biopsy. Liver core biopsy showed lymphocytic and foamy histiocytic infiltrates throughout the lobules, portal tract damage and focal loss of ducts, hepatitis, and bile ductular proliferation. Shortly after, the patient experienced encephalopathy, hypovolemic shock, and expired. Discussion: In critically ill adults, severe hyperbilirubinemia above 30 mg/dL is associated with multi-organ failure and a markedly increased risk of mortality. This patient presented without risk factors for chronic liver disease but was found to have acute liver failure in the setting of a recent viral infection and increased use of a hepatotoxic agent. Biopsy revealed a combination of liver insults, with lymphocytic infiltration and bile duct loss consistent with COVID-19 infection, and portal tract damage with interface hepatitis indicative of DILI. According to Food and Drug Administration reports, Artri King contains undisclosed diclofenac, dexamethasone and phenolphthalein, and is under scrutiny for potential liver toxicity. We demonstrate a potential synergistic effect between COVID-19 and DILI from Artri King supplement, leading to more severe liver injury than would be expected from either insult alone. This highlights the importance of thoroughly reviewing supplement use and maintaining a broad differential in evaluating any pattern of liver injury.

Authors

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001149304.90488.d4
Primary Topic
Drug-Induced Hepatotoxicity and Protection
Type
article
Field-Weighted Citation Impact
0.00
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article

S5461 A Fatal Synergy: Acute Liver Failure From COVID-19 and Herbal Supplement With Undeclared Ingredients

Michael Clores, Alan Abboud, Rahul Tripathi, Jordan Barnett-Kradjian
The American Journal of Gastroenterology
Drug-Induced Hepatotoxicity and Protection
article

S5461 A Fatal Synergy: Acute Liver Failure From COVID-19 and Herbal Supplement With Undeclared Ingredients

Michael Clores, Alan Abboud, Rahul Tripathi, Jordan Barnett-Kradjian
article en

Abstract

Introduction: Drug-induced liver injury (DILI) and viral infections are important considerations in the broad differential diagnosis of hepatobiliary injury, particularly after the exclusion of more common etiologies. We present a fatal case of biopsy-proven acute liver failure from concurrent Coronavirus 2019 (COVID-19) infection and DILI due to Artri King, an over-the-counter herbal supplement containing undisclosed hepatotoxic ingredients. Case Description/Methods: A 56-year-old man with systemic lupus erythematosus presented with abdominal distension and jaundice. The patient reported increased consumption of Artri King for joint pain and denied additional home medications. Labs demonstrated elevated total bilirubin (7.2 mg/dL), severe transaminitis (alanine aminotransferase 2,909 IU/L), low fibrinogen, low platelets, elevated international normalized ratio of 2, EBV reactivation, and positive SARS CoV-2 PCR. Negative workup included: computed tomography of the abdomen, urine and serum toxicology, viral and autoimmune serology, and hereditary causes. Within 24 hours of admission, the patient started an N-acetyl cystine protocol. Despite improvement in transaminases, total bilirubin continued to rise to 30.3 mg/dL prompting liver biopsy. Liver core biopsy showed lymphocytic and foamy histiocytic infiltrates throughout the lobules, portal tract damage and focal loss of ducts, hepatitis, and bile ductular proliferation. Shortly after, the patient experienced encephalopathy, hypovolemic shock, and expired. Discussion: In critically ill adults, severe hyperbilirubinemia above 30 mg/dL is associated with multi-organ failure and a markedly increased risk of mortality. This patient presented without risk factors for chronic liver disease but was found to have acute liver failure in the setting of a recent viral infection and increased use of a hepatotoxic agent. Biopsy revealed a combination of liver insults, with lymphocytic infiltration and bile duct loss consistent with COVID-19 infection, and portal tract damage with interface hepatitis indicative of DILI. According to Food and Drug Administration reports, Artri King contains undisclosed diclofenac, dexamethasone and phenolphthalein, and is under scrutiny for potential liver toxicity. We demonstrate a potential synergistic effect between COVID-19 and DILI from Artri King supplement, leading to more severe liver injury than would be expected from either insult alone. This highlights the importance of thoroughly reviewing supplement use and maintaining a broad differential in evaluating any pattern of liver injury.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 52%
Drug-Induced Hepatotoxicity and Protection
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