| Literature DB >> 11054759 |
K A Kleopa1, J W Teener, S S Scherer, S L Galetta, S J Bird.
Abstract
A patient presented with symptoms of limbic and brainstem encephalitis, motor and sensory neuronopathy, cerebellar dysfunction, and highly positive anti-Hu antibodies. He also harbored P/Q-type calcium channel antibodies and manifested the Lambert-Eaton myasthenic syndrome (LEMS). Small-cell lung cancer was found, and he received both antineoplastic therapy and intravenous immunoglobulin (IVIg). Remission of the malignancy was achieved. Although the anti-Hu-related manifestations improved after therapy, LEMS has persisted, leading to IVIg dependency. Copyright 2000 John Wiley & Sons, Inc.Entities:
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Year: 2000 PMID: 11054759 DOI: 10.1002/1097-4598(200011)23:11<1767::aid-mus16>3.0.co;2-a
Source DB: PubMed Journal: Muscle Nerve ISSN: 0148-639X Impact factor: 3.217