Methotrexate Toxicity Masquerading Section as Systemic Lupus Erythematosus Flare: A Case Report

A 36-year-old woman with Rheumatoid Arthritis (RA) and class V lupus nephritis presented with fever, dysphagia and oral mucosal bleeding. She had been prescribed Methotrexate (MTX) 15 mg weekly but used it irregularly-almost daily-for four months. On examination, she had oral ulcers, reduced mouth opening, diffuse hair thinning, and erythematous papules. Laboratory findings revealed severe pancytopenia, elevated liver enzymes, and an increased MTX level. Complement levels were normal and antidsDNA negative, making a Systemic Lupus Erythematosus (SLE) flare unlikely. The diagnosis of MTX toxicity was confirmed. She was managed with immediate MTX withdrawal, folinic acid rescue (15 mg i.v. every six hours for three days), blood transfusions, and supportive care. Her counts normalised, and mucositis resolved within two weeks. This case emphasises the diagnostic challenge in differentiating drug toxicity from disease flare in autoimmune patients and underscores the need for strict adherence to MTX monitoring guidelines.

Authors

Publication Details

Journal
JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH
Published
2025-10-17
DOI
https://doi.org/10.7860/jcdr/2025/82340.22048
Primary Topic
Chronic Lymphocytic Leukemia Research
Type
article
Field-Weighted Citation Impact
0.00
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article

Methotrexate Toxicity Masquerading Section as Systemic Lupus Erythematosus Flare: A Case Report

Sunil Kumar, Siddharth Shah, Yash Anand Chordia, Hem Menpara
JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH
Chronic Lymphocytic Leukemia Research
article

Methotrexate Toxicity Masquerading Section as Systemic Lupus Erythematosus Flare: A Case Report

Sunil Kumar, Siddharth Shah, Yash Anand Chordia, Hem Menpara
article en

Abstract

A 36-year-old woman with Rheumatoid Arthritis (RA) and class V lupus nephritis presented with fever, dysphagia and oral mucosal bleeding. She had been prescribed Methotrexate (MTX) 15 mg weekly but used it irregularly-almost daily-for four months. On examination, she had oral ulcers, reduced mouth opening, diffuse hair thinning, and erythematous papules. Laboratory findings revealed severe pancytopenia, elevated liver enzymes, and an increased MTX level. Complement levels were normal and antidsDNA negative, making a Systemic Lupus Erythematosus (SLE) flare unlikely. The diagnosis of MTX toxicity was confirmed. She was managed with immediate MTX withdrawal, folinic acid rescue (15 mg i.v. every six hours for three days), blood transfusions, and supportive care. Her counts normalised, and mucositis resolved within two weeks. This case emphasises the diagnostic challenge in differentiating drug toxicity from disease flare in autoimmune patients and underscores the need for strict adherence to MTX monitoring guidelines.

JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH
Openalex Percentile: Top 59%
Chronic Lymphocytic Leukemia Research
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