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Japanese

A Case of Syringomyelobulbia pp.267-272
Published Date 1957/4/1
DOI https://doi.org/10.11477/mf.1406200567
  • Abstract
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The authers reported the case of a 28 years old female who developed the syndrome of Syringomyelia accompanied with nystagmus and other bulbary symptoms.

From the onset of the disease the patient suffered from photophobia, dizziness, diplopia and weakness of the left upper extremity. There was a relatively slow progression of symptoms during the subsequent 13 years, until she started to complain of difficulty of the gait, tremor of the left hand, headache, bussing in the ears, nausea, vomiting, pers-piration and dyspnea.

The examination revealed the following positive findings:

bilateral Horner's syndrome, pendular nys-tagmus upon forward gaze and rotator Nys-tagmus upon lateral gaze, slow and nasal speach, atrophy and fascicular twitches of the tongue and the left thenar eminence, involuntary movements of the fingers of the left hand, dorsal Scoliosis, several scars due to burnings on the left forearm and the fin-gers of the left hand, hyperactive biceps and trices reflexes of the right but the negative reflexes of the left, hyperactive Knee and ankle reflexes, slightly positive Babinskis reflex and spastic-atactic gait.


Copyright © 1957, Igaku-Shoin Ltd. All rights reserved.

基本情報

電子版ISSN 2185-405X 印刷版ISSN 0006-8969 医学書院

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