Kleine–Levin syndrome elicited by encephalopathy with reversible splenial lesion

Kleine–Levin syndrome is a rare sleep disorder of unknown etiology characterized by repetitive episodes of hypersomnia between asymptomatic periods. We report the case of a 13‐year‐old girl who presented with drowsiness triggered by influenza A as the first episode. Magnetic resonance imaging (MRI)...

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Veröffentlicht in:Pediatrics international 2017-08, Vol.59 (8), p.929-931
Hauptverfasser: Takayanagi, Masaru, Okabe, Shinichi, Yamamoto, Katsuya, Komatsu, Juri, Suzuki, Rikio, Kitamura, Taro, Ohura, Toshihiro
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container_end_page 931
container_issue 8
container_start_page 929
container_title Pediatrics international
container_volume 59
creator Takayanagi, Masaru
Okabe, Shinichi
Yamamoto, Katsuya
Komatsu, Juri
Suzuki, Rikio
Kitamura, Taro
Ohura, Toshihiro
description Kleine–Levin syndrome is a rare sleep disorder of unknown etiology characterized by repetitive episodes of hypersomnia between asymptomatic periods. We report the case of a 13‐year‐old girl who presented with drowsiness triggered by influenza A as the first episode. Magnetic resonance imaging (MRI) on day 6 showed transient reduction of diffusion in the corpus callosum splenium. The patient was diagnosed with encephalopathy with a reversible splenial lesion. The symptoms resolved after 10 days, but additional episodes of hypersomnia lasting 5–10 days occurred 1, 5, 6, 11, 13, and 25 months after the first episode. MRI during hypersomnia indicated no lesions, and sleep duration and cognition were normal between episodes. The patient was diagnosed with Kleine–Levin syndrome. Electroencephalographic and clinical findings during the first episode were similar to those during the other episodes. Encephalopathy with a splenial lesion and Kleine–Levin syndrome may have similar pathological mechanisms causing a disturbance in consciousness.
doi_str_mv 10.1111/ped.13326
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We report the case of a 13‐year‐old girl who presented with drowsiness triggered by influenza A as the first episode. Magnetic resonance imaging (MRI) on day 6 showed transient reduction of diffusion in the corpus callosum splenium. The patient was diagnosed with encephalopathy with a reversible splenial lesion. The symptoms resolved after 10 days, but additional episodes of hypersomnia lasting 5–10 days occurred 1, 5, 6, 11, 13, and 25 months after the first episode. MRI during hypersomnia indicated no lesions, and sleep duration and cognition were normal between episodes. The patient was diagnosed with Kleine–Levin syndrome. Electroencephalographic and clinical findings during the first episode were similar to those during the other episodes. 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Medical Complete (Alumni)</collection><jtitle>Pediatrics international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takayanagi, Masaru</au><au>Okabe, Shinichi</au><au>Yamamoto, Katsuya</au><au>Komatsu, Juri</au><au>Suzuki, Rikio</au><au>Kitamura, Taro</au><au>Ohura, Toshihiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Kleine–Levin syndrome elicited by encephalopathy with reversible splenial lesion</atitle><jtitle>Pediatrics international</jtitle><addtitle>Pediatr Int</addtitle><date>2017-08</date><risdate>2017</risdate><volume>59</volume><issue>8</issue><spage>929</spage><epage>931</epage><pages>929-931</pages><issn>1328-8067</issn><eissn>1442-200X</eissn><abstract>Kleine–Levin syndrome is a rare sleep disorder of unknown etiology characterized by repetitive episodes of hypersomnia between asymptomatic periods. We report the case of a 13‐year‐old girl who presented with drowsiness triggered by influenza A as the first episode. Magnetic resonance imaging (MRI) on day 6 showed transient reduction of diffusion in the corpus callosum splenium. The patient was diagnosed with encephalopathy with a reversible splenial lesion. The symptoms resolved after 10 days, but additional episodes of hypersomnia lasting 5–10 days occurred 1, 5, 6, 11, 13, and 25 months after the first episode. MRI during hypersomnia indicated no lesions, and sleep duration and cognition were normal between episodes. The patient was diagnosed with Kleine–Levin syndrome. Electroencephalographic and clinical findings during the first episode were similar to those during the other episodes. Encephalopathy with a splenial lesion and Kleine–Levin syndrome may have similar pathological mechanisms causing a disturbance in consciousness.</abstract><cop>Australia</cop><pub>Blackwell Publishing Ltd</pub><pmid>28804979</pmid><doi>10.1111/ped.13326</doi><tpages>3</tpages></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Adolescent
Brain Diseases
clinically mild encephalitis/encephalopathy with a reversible splenial lesion
Cognition
Consciousness
Corpus callosum
Corpus Callosum - diagnostic imaging
Drowsiness
EEG
Encephalitis, Viral - complications
Encephalitis, Viral - diagnostic imaging
Encephalopathy
Etiology
Fatigue
Female
Humans
Hypersomnia
Influenza A
Influenza A virus
influenza encephalopathy
Influenza, Human - complications
Influenza, Human - diagnosis
Kleine-Levin Syndrome - diagnostic imaging
Kleine-Levin Syndrome - etiology
Lesions
Magnetic Resonance Imaging
Neuroimaging
NMR
Nuclear magnetic resonance
Pediatrics
periodic hypersomnolence
recurrent hypersomnia
Sleep
Sleep disorders
title Kleine–Levin syndrome elicited by encephalopathy with reversible splenial lesion
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