Journals / Journal of Neurological Sciences (Turkish) / 2009 / Cilt: 26 - Sayı: 3

Lambert-eaton myastenik sendromunun eşlik ettiği subakut serebellar dejenerasyon vakası

A case of subacute cerebellar degeneration coexisting with lambert-eaton myastenic syndrome

Pages
371–375
Publication Date
2022-10-19
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

We present here a case with symptoms of subacute cerebellar degeneration coexisting with LEMS.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Paraneoplastic cerebellar degeneration (PCD) is a neurological disorder characterized by the subacute onset of cerebellar dysfunction, sometimes with dysarthria, dysphagia, nystagmus, mental changes, muscular and sensory deficits.
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Key Findings & Data:Cancers of the lung, ovary, breast and lymphoma are the most frequent causal neoplasms.
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Conclusion & Impact:We present here a case with symptoms of subacute cerebellar degeneration coexisting with LEMS.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Paraneoplastic cerebellar degeneration (PCD) is a neurological disorder characterized by the subacute onset of cerebellar dysfunction, sometimes with dysarthria, dysphagia, nystagmus, mental changes, muscular and sensory deficits. Cancers of the lung, ovary, breast and lymphoma are the most frequent causal neoplasms. Furthermore, PCD may occur in association with the Lambert- Eaton myasthenic syndrome (LEMS). LEMS is a rare syndrome with fluctuating muscle weakness, hyporeflexia and autonomic dysfunction, predominantly effecting men. We present here a case with symptoms of subacute cerebellar degeneration coexisting with LEMS.

Özet

Paraneoplastik serebellar dejenerasyon (PSD), subakut serebellar bozukluğa eşlik eden dizartri, disfaji, nistagmus, mental değişiklikler, parezi ve duysal defisitlerle karakterize bir nörolojik bozukluktur. En sık akciğer, over, meme kanserleri ve lenfomalarla birliktelik gösterir. Ayrıca Lambert-Eaton myastenik sendromu (LEMS) ile de birlikteliği bilinmektedir. LEMS dalgalanan kas güçsüzlüğü, hiporefleksi ve otonomik bozukluklarla giden ve en fazla erkekleri etkileyen nadir görülen bir sendromdur. Bu makalede, subakut serebellar dejenerasyon bulguları ile birliktelik gösteren bir LEMS vakası sunulmuştur.

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Cite This Article

CELİK, M., ORKEN, D. N., ACAR, S., KENANGİL, G. (2022). Lambert-eaton myastenik sendromunun eşlik ettiği subakut serebellar dejenerasyon vakası. Journal of Neurological Sciences (Turkish), Cilt: 26 - Sayı: 3, 371–375. https://ajindex.com/articles/565489

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References (15)

  1. Anderson HJ, Churchill-Davidson HC, Richardson AT. Bronchial neoplasm with myasthenia: prolonged apnea after administration of succinylcholine. Lancet 1953;19:1291-93
  2. Bain PG, Motomura M, Newsom-Davis J, Misbah SA, Chapel HM, Lee ML, Vincent A, Lang B. Effects of intravenous immunglobulin on muscle weakness and calcium-channel autoantibodies in the Lambert-Eaton myasthenic syndrome. Neurology 1996; 47: 678-83
  3. Bird SJ. Clinical and electrophysiological improvement in Lambert-Eaton syndrome with intravenous immunglobulin therapy. Neurology 1992; 42: 1422-23
  4. Brain WR, Wilkinson M. Subacute cerebellar degeneration associated with neoplasms. Brain 1965; 88: 465-78
  5. Burns TM, Juel VC, Sanders DB, Phillips LH II. Neuroendocrine lung tumors and disorders of neuromuscular junction. Neurology 1999; 52: 1490- 91
  6. Clouston PD, Saper CB, Arbizu T, Johnston I, Lang B, Newsom-Davis J, Posner JB. Paraneoplastic cerebellar degeneration. III. Cerebellar degeneration, cancer and the Lambert-Eaton myasthenic syndrome. Neurology 1992; 42: 1944-50
  7. Henson RA. Discussion of unusual manifestations of bronchial carcinoma. Proceedings of the Royal Society of medicine 1953; 46: 859-61
  8. Hawley RJ, Cohen MH, Saini N, Armbrustmacher VW. The carcinomatous neuromyopathy of oat cell lung cancer. Ann Neurol 1980; 7: 65-72
  9. Illa I. IVIg in myasthenia gravis, Lambert Eaton myasthenic syndrome and inflammatory myopathies: current status. J Neurol 2005; 252: 14-18
  10. Lambert EH, Eaton LM, Rooke ED. Defect of neuromuscular conduction associated with malignant neoplasms. Am J Physiology 1956; 187: 612-13
  11. Lambert EH, Rooke ED. Myasthenic state and lung cancer. In: The remote effects of Cancer on the nervous system. Ed’s, Brain WR, Norris FH, Grune and Stratton, 1965, pp: 67-80
  12. Lee J-H, Shin J-H, Kim D-S, Jung DS, Park K-H, Lee M-K, Kim J-Y. A case of Lambert-Eaton Myasthenic Syndrome associated with atypical bronchopulmonary carcinoid tumor. J Korean Med Sci 2004; 19: 753-55
  13. Maddison P, Lang B, Mills K, Newsom-Davis J. Long term outcome in Lambert-Eaton myasthenic syndrome without lung cancer. J Neurol Neurosurg Psychiatry 2001; 70: 212-17
  14. Mason WP, Graus F, Lang B, Honnorat J, Delattre J-Y, Valldeoriola F, Antoine JC, Rosenblum MK, Rosenfeld MR, Newsom-Davis J, Posner JB, Dalmau J. Small-cell lung cancer, pareneoplastic cerebellar degeneration and Lambert-Eaton myasthenic syndrome. Brain 1997; 120: 1279-300
  15. Motamura M, Lang B, Johnson I, P