Evidence map›Paper›PMID 41291493›Full record

ArticleBMC neurology2025

Lambert-Eaton myasthenic syndrome presenting with occult mediastinal small cell carcinoma and positivity for anti-CV2/CRMP5 and anti-SOX1 antibodies: a case report.

Anna Wang, He Li, Dewen Li, Kangfeng Wang, Lijuan Zhang

Abstract readCase Reports
In one paragraph

Article in BMC neurology, 2025. 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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5 · Who and what money

Authors and funding

5 authors.

Anna Wang *First School of Clinical Medicine, Shandong University of Traditional Chinese Medicine, Jinan, 250014, China.
He Li *Neurology Department, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, 250014, China.
Dewen LiShandong Academy of Agricultural Sciences Health Service Center, Jinan, 250014, China.
Kangfeng WangNeurology Department, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, 250014, China. wkf6@163.com.
Lijuan ZhangPsychosomatic Medicine, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, 250014, China. zhlj-8103@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLambert-Eaton myasthenic syndrome (LEMS) is a rare autoimmune neuromuscular disorder characterized by proximal muscle weakness, autonomic dysfunction and hyporeflexia. Numerous studies have reported the association of LEMS with anti-SOX1 antibodies and small cell carcinoma, but LEMS with double antibody positivity and cerebellar ataxia accompanied by small cell carcinoma is relatively rare. CASE PRESENTATION: A 56-year-old female patient developed progressive limb weakness in November 2023, with symptoms gradually worsening over six months to include gait instability, impaired grip, chest tightness, dyspnea, dysphagia, and aspiration. Electrodiagnostic testing confirmed Lambert-Eaton myasthenic syndrome (LEMS) with positive VGCC antibodies. Paraneoplastic antibody testing showed positive anti-CV2/CRMP5 antibodies (24 AU) and borderline anti-SOX1 antibodies (9 AU), while other antibodies were negative. Initial imaging (contrast-enhanced chest CT and PET-CT) revealed no abnormalities, but follow-up one year later detected mediastinal small cell lung cancer. The patient underwent three plasma exchange sessions with corticosteroid therapy with limited response, then showed significant improvement after switching to subcutaneous Telitacicept (80 mg) combined with Fampyra Comprimidos and Mycophenolate Mofetil capsules, achieving independent ambulation and normal grip strength with only mild residual limb weakness. The patient has since been transferred to a local hospital for chemotherapy.

conclusionWe find that LEMS with concurrent anti-SOX1 and anti-CV2/CRMP5 positivity manifests as rapid progression, prominent proximal weakness, and potential cerebellar and autonomic involvement. Early and sustained oncological surveillance—particularly of mediastinal lymph nodes—and combined immunotherapeutic strategies can significantly improve neurological outcomes.

Indexed as

AutoantibodiesCarcinoma, Small CellHydrolasesLambert-Eaton Myasthenic SyndromeMediastinal NeoplasmsNerve Tissue ProteinsSOXB1 Transcription FactorsFemaleHumansMicrotubule-Associated ProteinsMiddle AgedAutoantibodiesDPYSL5 protein, humanHydrolasesMicrotubule-Associated ProteinsNerve Tissue ProteinsSOX1 protein, humanSOXB1 Transcription FactorsCase reportCerebellar ataxiaLambert–Eaton myasthenic syndromeOccult mediastinal small cell carcinoma

Identifiers

PMID41291493
PMCPMC12764000

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