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Neuroleptic malignant syndrome after penetrating keratoplasty in a case of Parkinson disease Mika Shinoda 1 , Masahiko Kozawa 1 , Jun Kajiwara 1 , Shigeki Nabeshima 2 , Eiichi Uchio 1 1Dept of Ophthalmol, Fukuoka Univ Sch of Med 2Dept of Gen Med, Fukuoka Univ Sch of Med pp.1733-1736
Published Date 2013/10/15
DOI https://doi.org/10.11477/mf.1410104948
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Abstract. Purpose:To report a case of Parkinson disease who developed neuroleptic malignant syndrome after penetrating keratoplasty. Case:A 69-year-old male was referred to us for corneal edema in both eyes. Corneal edema seemed to be due to amantadin that he was receiving for Parkinson disease. Findings:Corrected visual acuity was 0.05 right and 0.03 left. Both eyes showed corneal edema. He underwent penetrating keratoplasty, lens extraction and intraocular lens insertion in the left eye under general anesthesia. He developed severe sweating, tremor, myotonia and unconsciousness the same evening of surgery. Postoperative delirium was initially suspected. He showed elevated serum level of creatine kinase 12 days after surgery and was diagnosed with neuroleptic malignant syndrome. He started receiving dantrolen 3 days later but the general status worsened. He passed away 28 days after surgery. Conclusion:The present case illustrates that neuroleptic malignant syndrome may develop while under treatment for Parkinson disease.


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電子版ISSN 1882-1308 印刷版ISSN 0370-5579 医学書院

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