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Kleine–Levin syndrome elicited by encephalopathy with reversible splenial lesion
Author(s) -
Takayanagi Masaru,
Okabe Shinichi,
Yamamoto Katsuya,
Komatsu Juri,
Suzuki Rikio,
Kitamura Taro,
Ohura Toshihiro
Publication year - 2017
Publication title -
pediatrics international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.49
H-Index - 63
eISSN - 1442-200X
pISSN - 1328-8067
DOI - 10.1111/ped.13326
Subject(s) - medicine , splenium , corpus callosum , encephalopathy , lesion , etiology , asymptomatic , pathological , pediatrics , magnetic resonance imaging , pathology , radiology , white matter
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.