Evidence map›Paper›PMID 42854056›Full record

ArticleMedicine2026

Lamotrigine-associated SJS/TEN overlap during valproate co-therapy managed with rhTNFR-Fc and therapeutic plasma exchange: A case report.

Fang Chen, Xiao Li

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In one paragraph

Article in Medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Fang ChenDepartment of Dermatovenereology, Leshan Hospital of Traditional Chinese Medicine, Affiliated to Chengdu University of Chinese Medicine, Leshan, Sichuan, People's Republic of China.ORCID 0009-0002-3264-8373
Xiao LiIntensive Care Unit, Leshan Hospital of Traditional Chinese Medicine, Affiliated to Chengdu University of Chinese Medicine, Leshan, Sichuan, People's Republic of China.ORCID 0009-0000-5578-9764

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleStevens-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.

interventionsDuring 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.

Indexed as

AnticonvulsantsEtanerceptLamotriginePlasma ExchangeStevens-Johnson SyndromeValproic AcidDrug Therapy, CombinationHumansMaleMiddle AgedAnticonvulsantsEtanerceptLamotrigineValproic Acidlamotriginesevere cutaneous adverse reactionSJS/TEN overlaptherapeutic plasma exchangeTNF-alpha inhibitor

Identifiers

PMID42854056
PMCPMC13657496

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