# Rituximab-Associated Liver Toxicity Without Known Viral Reactivation

**Authors:** Taha Huda, Fawaz Hussain, Hariharasudan Mani, Shereen M Gheith, Savitri Skandan

PMC · DOI: 10.7759/cureus.64331 · 2024-07-11

## TL;DR

A patient developed severe liver injury after receiving rituximab, but no viral reactivation was found as a cause.

## Contribution

This case report highlights a rare instance of rituximab-induced liver toxicity without viral reactivation.

## Key findings

- A patient with marginal zone B-cell lymphoma experienced significant liver injury after rituximab treatment.
- No evidence of viral reactivation was found despite the liver injury.
- This case suggests rituximab can cause hepatotoxicity independent of viral reactivation.

## Abstract

Rituximab is a targeted immunotherapeutic agent that has demonstrated efficacy in treating CD20+ B-cell neoplasms as well as other lymphoproliferative and autoimmune disorders. A major adverse effect of rituximab is hepatocellular injury attributed to hepatitis B viral reactivation, necessitating viral titers before treatment. In this case report, we illustrate the rare presentation of a patient with marginal zone B-cell lymphoma who experienced symptomatic liver injury with a peak 15-fold aminotransferase elevation following his first dose of rituximab, without evidence of viral reactivation.

## Linked entities

- **Proteins:** MS4A1 (membrane spanning 4-domains A1)
- **Diseases:** marginal zone B-cell lymphoma (MONDO:0017604), hepatitis B (MONDO:0005344)

## Full-text entities

- **Genes:** KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}
- **Diseases:** Liver Toxicity (MESH:D056486), liver injury (MESH:D017093), lymphoproliferative and autoimmune disorders (MESH:D056735), marginal zone B-cell lymphoma (MESH:D018442), B-cell neoplasms (MESH:D016393)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11316497/full.md

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Source: https://tomesphere.com/paper/PMC11316497