| Literature DB >> 25680985 |
Kodai Kume1, Kazushi Deguchi2, Kazuyo Ikeda3, Tadayuki Takata1, Yohei Kokudo1, Masaki Kamada3, Tetsuo Touge4, Toshiyuki Takahashi5, Takashi Kanbayashi6, Tsutomu Masaki1.
Abstract
We report the case of a 46-year-old Japanese woman with neuromyelitis optica spectrum disorder presenting with repeated hypersomnia accompanied by decreased CSF orexin level. First episode associated with hypothalamic-pituitary dysfunction showed bilateral hypothalamic lesions that can cause secondary damage to the orexin neurons. The second episode associated with impaired memory showed a left temporal lesion involving the amygdala. The mechanism remains unknown, but the reduced blood flow in the hypothalamus ipsilateral to the amygdala lesion suggested trans-synaptic hypothalamic dysfunction secondary to the impaired amygdala. A temporal lesion involving the amygdala and hypothalamus could be responsible for hypersomnia due to neuromyelitis optica spectrum disorder.Entities:
Keywords: Neuromyelitis optica spectrum disorder; amygdala; aquaporin 4; hypersomnia; hypothalamus; orexin
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Year: 2015 PMID: 25680985 DOI: 10.1177/1352458515569100
Source DB: PubMed Journal: Mult Scler ISSN: 1352-4585 Impact factor: 6.312