Literature DB >> 18468847

A case of Creutzfeldt-Jacob disease with bilateral vocal fold abductor paralysis.

Lishu Li1, Hideto Saigusa, Hiroshi Nagayama, Tsuyoshi Nakamura, Iichirou Aino, Taro Komachi, Satoshi Yamaguchi.   

Abstract

Bilateral vocal fold abductor paralysis was seen in a patient with Creutzfeldt-Jacob disease. After tracheotomy, the patient showed disappearance of reduced oxygen saturation with high-pitched inspiratory stridor and pulling phenomenon of the supraclavicular region and larynx. Electromyographic examinations of the intrinsic laryngeal muscles, including the thyroarytenoid and posterior cricoarytenoid muscles, demonstrated that there was no apparent action potential in those muscles during spontaneous respiratory movements, and there was no abnormal potential for those muscles at rest. By pushing the infrasternal region of the patient on the expiration, normal motor unit action potential could be seen in the posterior cricoarytenoid muscle on the next inspiration. Based on those findings, we concluded that bilateral vocal fold abductor paralysis in this case of Creutzfeldt-Jacob disease was not induced by disorders of the degeneration of motor nucleus in the ambiguus as in multiple system atrophy, but by a disorder of the upper motor neuron.

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Year:  2008        PMID: 18468847     DOI: 10.1016/j.jvoice.2008.02.002

Source DB:  PubMed          Journal:  J Voice        ISSN: 0892-1997            Impact factor:   2.009


  1 in total

1.  Multifocal hits for propagation of prion protein in sporadic Creutzfeldt-Jakob disease.

Authors:  Kensaku Kasuga; Ryoko Takeuchi; Toshiaki Takahashi; Nae Matsubara; Ryoko Koike; Akio Yokoseki; Masatoyo Nishizawa
Journal:  Neurol Neuroimmunol Neuroinflamm       Date:  2014-12-23
  1 in total

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