Late onset cerebellar ataxia syndrome after non-paraneoplastic Lambert-Eaton myasthenic syndrome: a case study

Abstract This is an unusual case of voltage gated calcium channel (VGCC) antibodies leading to two distinct and chronologically separated neurologic syndromes without the presence of an underlying neoplasm. Lambert Eaton Myasthenic Syndrome (LEMS) presented five years prior to cerebellar ataxia. Bot...

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Main Authors: David P. Randall, Matthew C. Randall
Format: Article
Language:English
Published: BMC 2025-01-01
Series:BMC Neurology
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Online Access:https://doi.org/10.1186/s12883-024-03983-8
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author David P. Randall
Matthew C. Randall
author_facet David P. Randall
Matthew C. Randall
author_sort David P. Randall
collection DOAJ
description Abstract This is an unusual case of voltage gated calcium channel (VGCC) antibodies leading to two distinct and chronologically separated neurologic syndromes without the presence of an underlying neoplasm. Lambert Eaton Myasthenic Syndrome (LEMS) presented five years prior to cerebellar ataxia. Both LEMS and cerebellar ataxia were responsive to treatment, but not the same therapy. He was diagnosed with LEMS through history, exam, electromyography/nerve conduction studies (EMG/NCS) with repetitive nerve stimulation (RNS) and antibody testing. He was treated with 3,4 diaminopyridine (3,4 DAP) with an excellent response. Five years later, he developed acute ataxia. The patient required months of intensive and continued immunomodulating therapy.
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spelling doaj-art-f5f8a376c43b437bb9d8ac404c6969212025-01-05T12:34:06ZengBMCBMC Neurology1471-23772025-01-012511310.1186/s12883-024-03983-8Late onset cerebellar ataxia syndrome after non-paraneoplastic Lambert-Eaton myasthenic syndrome: a case studyDavid P. Randall0Matthew C. Randall1Neuromuscular Neurology, Advocate HealthNeuromuscular Neurology, Advocate HealthAbstract This is an unusual case of voltage gated calcium channel (VGCC) antibodies leading to two distinct and chronologically separated neurologic syndromes without the presence of an underlying neoplasm. Lambert Eaton Myasthenic Syndrome (LEMS) presented five years prior to cerebellar ataxia. Both LEMS and cerebellar ataxia were responsive to treatment, but not the same therapy. He was diagnosed with LEMS through history, exam, electromyography/nerve conduction studies (EMG/NCS) with repetitive nerve stimulation (RNS) and antibody testing. He was treated with 3,4 diaminopyridine (3,4 DAP) with an excellent response. Five years later, he developed acute ataxia. The patient required months of intensive and continued immunomodulating therapy.https://doi.org/10.1186/s12883-024-03983-8Lambert-Eaton myasthenic syndromeCerebellar ataxiaVoltage-gated calcium channel antibodiesParaneoplastic cerebellar syndrome
spellingShingle David P. Randall
Matthew C. Randall
Late onset cerebellar ataxia syndrome after non-paraneoplastic Lambert-Eaton myasthenic syndrome: a case study
BMC Neurology
Lambert-Eaton myasthenic syndrome
Cerebellar ataxia
Voltage-gated calcium channel antibodies
Paraneoplastic cerebellar syndrome
title Late onset cerebellar ataxia syndrome after non-paraneoplastic Lambert-Eaton myasthenic syndrome: a case study
title_full Late onset cerebellar ataxia syndrome after non-paraneoplastic Lambert-Eaton myasthenic syndrome: a case study
title_fullStr Late onset cerebellar ataxia syndrome after non-paraneoplastic Lambert-Eaton myasthenic syndrome: a case study
title_full_unstemmed Late onset cerebellar ataxia syndrome after non-paraneoplastic Lambert-Eaton myasthenic syndrome: a case study
title_short Late onset cerebellar ataxia syndrome after non-paraneoplastic Lambert-Eaton myasthenic syndrome: a case study
title_sort late onset cerebellar ataxia syndrome after non paraneoplastic lambert eaton myasthenic syndrome a case study
topic Lambert-Eaton myasthenic syndrome
Cerebellar ataxia
Voltage-gated calcium channel antibodies
Paraneoplastic cerebellar syndrome
url https://doi.org/10.1186/s12883-024-03983-8
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