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도약잘린끝(Jumping Stump)증후군을 모방한 항-LGI1항체뇌염

Anti-LGI1 Antibody Encephalitis Mimicking Jumping Stump Syndrome

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초록

Jumping stump syndrome is considered to be a peripherally induced movement disorder due to damage to peripheral nerves leading to dystonia or myoclonus. Anti-leucine-rich glioma-inactivated 1 antibody (anti-LGI 1 Ab) encephalitis is clinically characterized with progressive cognitive dysfunction and seizure including facial brachial dystonic seizure. We report a case of a woman with a history of intractable involuntary movement on amputated forearm diagnosed as anti-LGI 1 Ab encephalitis, mimicking symptoms of jumping stump syndrome.

Abstract

Jumping stump syndrome is considered to be a peripherally induced movement disorder due to damage to peripheral nerves leading to dystonia or myoclonus. Anti-leucine-rich glioma-inactivated 1 antibody (anti-LGI 1 Ab) encephalitis is clinically characterized with progressive cognitive dysfunction and seizure including facial brachial dystonic seizure. We report a case of a woman with a history of intractable involuntary movement on amputated forearm diagnosed as anti-LGI 1 Ab encephalitis, mimicking symptoms of jumping stump syndrome.

참고문헌 (9)

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  8. Thompson J, "The importance of early immunotherapy in patients with faciobrachial dystonic seizures", Brain, 141, pp.348~356 (2017)
  9. Szots M, "Natural course of LGI1 encephalitis : 3–5 years of follow-up without immunotherapy", J Neurol Sci, 343, pp.198~202 (2014)

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