Medicine
October 9, 2026 · via Europe PMC
Lamotrigine-associated SJS/TEN overlap during valproate co-therapy managed with rhTNFR-Fc and therapeutic plasma exchange: A case report.
Chen F, Li X
AI summary — for doctors, generated from the abstract only
A patient developed lamotrigine-associated SJS/TEN overlap when lamotrigine was started at a full initial dose alongside valproate, and recovered after escalated therapy.
What was studied
A case report of a 49-year-old man with a rash and fever after starting lamotrigine 50 mg daily during valproate co-therapy, who progressed to SJS/TEN overlap with about 17% skin detachment.
Key findings
- Drug causality for lamotrigine was scored as probable, and lamotrigine was continued for the first two days before being stopped.
- IVIG and methylprednisolone gave only transient improvement, and he relapsed during steroid taper.
- Recombinant TNF receptor-Fc and three plasma exchange sessions with steroids cleared the eruption, with no relapse at 3 months.
Clinical relevance
Reinforces the need for reduced lamotrigine starting doses and slow titration with valproate, and early recognition of severe drug reactions.
Who should care
Limitations
A single case where several treatments were given in sequence, so no conclusion can be drawn about which therapy worked, and skin biopsy was declined.
Follow dose-reduction and slow-titration guidance when combining lamotrigine with valproate and stop the drug promptly if a severe rash appears.
This is an AI-generated summary of the published abstract, not a clinical recommendation. It may not reflect the full text or subsequent updates — verify against the original source before acting on it.
Abstract
RATIONALE
Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) is a rare, life-threatening severe cutaneous adverse reaction. Evidence for escalation therapy in relapsing disease remains limited.
PATIENT CONCERNS
A 49-year-old man developed fever and a rapidly progressive generalized erythematous maculopapular eruption after lamotrigine was initiated directly at 50 mg once daily during concomitant valproate therapy.
DIAGNOSES
At admission on August 3, 2023, no epidermal detachment was observed and SJS/TEN was not clinically recognized. On August 9 (hospital day 7), epidermal fragility, small blisters, and a positive Nikolsky sign led to recognition of the SJS/TEN spectrum, with detachment below 10%. Severity-of-illness score for toxic epidermal necrolysis was 1 at that time; age > 40 years was the only positive criterion. By day 12, detachment reached approximately 17% of the body surface area, supporting SJS/TEN overlap. The algorithm of drug causality for epidermal necrolysis score for lamotrigine was 5 (probable). Skin biopsy was declined.
INTERVENTIONS
During the initial diagnostic uncertainty on hospital days 1 and 2, lamotrigine was continued; it was discontinued on day 3 when a severe drug eruption was suspected. Intravenous immunoglobulin and intravenous methylprednisolone produced transient improvement. New epidermal detachment prompted methylprednisolone escalation and recombinant human tumor necrosis factor receptor-Fc fusion protein treatment. Relapse during corticosteroid tapering prompted 3 therapeutic plasma exchange sessions while corticosteroid therapy continued.
OUTCOMES
Three therapeutic plasma exchange sessions were subsequently administered with continued corticosteroid therapy, after which the eruption cleared. The patient was discharged on hospital day 33 and had no relapse or reported sequelae at 3-month follow-up.
LESSONS
This case illustrates the evolution from a severe drug eruption to SJS/TEN overlap, reinforces the importance of reduced lamotrigine starting doses and slow titration during valproate co-therapy, and provides a clinical example of stepwise multidisciplinary rescue management in relapsing disease.
DOI
10.1097/MD.0000000000051050
PMID
42854056
Research metadata (titles, abstracts, authors, publication dates) is sourced from Europe PMC, which aggregates content from PubMed/MEDLINE, PubMed Central, and other providers under the U.S. National Library of Medicine (NLM/NCBI). NLM does not claim copyright on abstracts; the original journal publishers or authors may hold rights to the full articles. AI-generated summaries are derived only from the abstract, never the full text, and are always labeled as AI-generated.
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