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Japanese

Polyneuropathy with skin pigmentation, hypertrichosis, lymphadenectasis, hepatomegaly, papilledema and monoclonal gammopathy: Report of an autopsy case Tadao TSUBAKI 1 , Yasuo TSUKADA 1 , Yo HORIKAWA 1 , Fusahiro IKUTA 2 1Department of Neurology, Brain Research Institute, Niigata University 2Department of Neuropathology, Brain Research Institute, Niigata University pp.747-749
Published Date 1976/8/10
DOI https://doi.org/10.11477/mf.1431903875
  • Abstract
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 A 35 year-old female patient first noted gait disturbance and swelling of subaxillar lymphnodules in the summer of 1965. The gait disturbance gradually progressed and in two years she noted hypertrichosis, dysmenorrhea, calves muscle pain and skin pigmentation.

 In August, 1967, she visited the outpatient clinic of the Department of Neurology, Niigata University Hospital. Neurological examination revealed muscle weakness and hypesthesia of the extremities and diminished or absent deep reflexes.


Copyright © 1976, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1243 印刷版ISSN 0001-8724 医学書院

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