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A Case of a Patient with Heterozygous Familial Hypercholesterolemia Whose Treatment was Gradually Reduced in Degree from LDL-apheresis Therapy to Mere Lipid-lowering Drug Therapy Seiichiro Yamasaki 1 , Shizuma Egashira 1 1Itoshima Medical Association Hospital, Atherosclerosis & Metabolic Research Keyword: LDLアフェレーシス , 家族性高コレステロール血症 , アキレス腱黄色腫退縮 , regression of achilles xanthoma , LDL-apheresis , familial hypercholesteloremia pp.599-602
Published Date 1994/6/15
DOI https://doi.org/10.11477/mf.1404900884
  • Abstract
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We present the case of a 56 year-old male with heterozygous familial hypercholesteloremia (type Ⅱa) weaned from LDL-apheresis treatment with the Liposorber system (Kaneka Corporation) combined with lipid-lowering drugs, untile he was able to manage with drug therapy only. The patient had an attack of angina pectoris at 48 years of age (November 1985) and was given lipid-lowering drug therapy consisting of probucol (750 mg/day) for two years. However, the therapy did not sufficiently reduce his serum cholesterol level below 395 mg/dl.


Copyright © 1994, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1200 印刷版ISSN 0452-3458 医学書院

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