ArticleCureus2025
Hydroxychloroquine-Induced Hepatotoxicity in Systemic Lupus Erythematous: A Case Report and Literature Review.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Mitigating Hydroxychloroquine-Induced Oxidative Liver Damage: The Roles of Adenosine Triphosphate, Liv-52, and Their Combination in Rats.International journal of molecular sciences · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Hydroxychloroquine (HCQ) is a medication that is commonly used as an antimalarial or disease-modifying anti-rheumatic drug (DMARD). Adverse side effects typically include retinal damage, cardiomyopathy, and neuromyopathy. However, there has been relatively little documentation on the effects of HCQ toxicity on the liver. We describe a case of HCQ-induced hepatic failure in a 31-year-old female patient on HCQ for systemic lupus erythematous who presented with three days of fever, diarrhea, and non-bilious, non-bloody vomiting. Labs showed massively elevated liver function tests (LFTs) and negative viral serology. The abdominal ultrasound and magnetic resonance cholangiopancreatography were unremarkable. A liver biopsy showed portal tracts with mild to moderate expansion by mixed inflammatory infiltrates, including scattered eosinophils and rare plasma cells with occasional mild interface activity focally close to bridging inflammation. These findings are consistent with drug-induced liver injury (DILI). HCQ was subsequently held, and the patient was admitted to the ICU for conservative management. Repeat LFTs showed down-trending over the course of the patient's four days of admission after discontinuation of HCQ and returned to baseline within a two-month timeframe.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.