左室機能低下を来した遺伝性ヘモクロマトーシスの1例

29歳,男性.歩行中の意識消失発作にて救急搬送.来院時神経学的所見正常.心房細動,心機能低下に加え,血清フェリチン異常高値,肝酵素上昇を認めた.本例は13歳時にhereditary hemochromatosis(HH)と診断,加療されるも19歳時より自己中断.HHによる心機能障害と考え,心不全の薬物治療に加え除鉄を施行.遺伝子検査にてHemojuvelin(HJV)遺伝子異常によるHHと診断.加療により血清フェリチン,肝機能,心不全症状は改善し外来通院中である....

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Published in日本内科学会雑誌 Vol. 101; no. 4; pp. 1069 - 1071
Main Authors 友安, 茂, 杉田, 純一, 鈴木, 憲史, 岩山, 香坂, 前田, 崇, 福島, 和之, 池ノ内, 浩
Format Journal Article
LanguageJapanese
Published 一般社団法人 日本内科学会 2012
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Online AccessGet full text
ISSN0021-5384
1883-2083
DOI10.2169/naika.101.1069

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Abstract 29歳,男性.歩行中の意識消失発作にて救急搬送.来院時神経学的所見正常.心房細動,心機能低下に加え,血清フェリチン異常高値,肝酵素上昇を認めた.本例は13歳時にhereditary hemochromatosis(HH)と診断,加療されるも19歳時より自己中断.HHによる心機能障害と考え,心不全の薬物治療に加え除鉄を施行.遺伝子検査にてHemojuvelin(HJV)遺伝子異常によるHHと診断.加療により血清フェリチン,肝機能,心不全症状は改善し外来通院中である.
AbstractList 29歳,男性.歩行中の意識消失発作にて救急搬送.来院時神経学的所見正常.心房細動,心機能低下に加え,血清フェリチン異常高値,肝酵素上昇を認めた.本例は13歳時にhereditary hemochromatosis(HH)と診断,加療されるも19歳時より自己中断.HHによる心機能障害と考え,心不全の薬物治療に加え除鉄を施行.遺伝子検査にてHemojuvelin(HJV)遺伝子異常によるHHと診断.加療により血清フェリチン,肝機能,心不全症状は改善し外来通院中である.
Author 杉田, 純一
鈴木, 憲史
友安, 茂
前田, 崇
岩山, 香坂
池ノ内, 浩
福島, 和之
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  fullname: 友安, 茂
  organization: 昭和大学病院血液内科
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  fullname: 杉田, 純一
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  fullname: 鈴木, 憲史
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  fullname: 岩山, 香坂
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  fullname: 前田, 崇
  organization: 昭和大学病院血液内科
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  fullname: 福島, 和之
  organization: 日本赤十字社医療センター循環器内科
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  fullname: 池ノ内, 浩
  organization: 日本赤十字社医療センター循環器内科
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References 6) Hayashi H, et al: Genetic Background of Primary Iron Overload Syndromes in Japan. Internal Medicine 45 (20): 1107-1111, 2006.
1) Hachiya M, et al: Hereditary Hemochromatosis Not Associated with Common HFE Gene Mutation in Japanese Siblings. Journal of Pediatric Gastroenterology and Nutrition 32: 501-503, 2001.
5) Hayashi H, et al: Genetic background of Japanese patients with adult-onset storage diseases in the liver. Hepatology Research 37: 777-783, 2007.
2) Koyama C, et al: Three patients with middle-age-onset hemochromatosis caused by novel mutations in the hemojuvelin gene. Journal of Hepatology 43: 740-742, 2005.
3) Nagayoshi Y, et al: A Q312X mutation in the hemojuvelin gene is associated withcardiomyopathy due to juvenile haemochromatosis. European Journal of Heart Failure 10: 1001-1006, 2008.
4) Kaneko Y, et al: Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders. J Gastroenterol 45: 1163-1171, 2010.
References_xml – reference: 1) Hachiya M, et al: Hereditary Hemochromatosis Not Associated with Common HFE Gene Mutation in Japanese Siblings. Journal of Pediatric Gastroenterology and Nutrition 32: 501-503, 2001.
– reference: 2) Koyama C, et al: Three patients with middle-age-onset hemochromatosis caused by novel mutations in the hemojuvelin gene. Journal of Hepatology 43: 740-742, 2005.
– reference: 4) Kaneko Y, et al: Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders. J Gastroenterol 45: 1163-1171, 2010.
– reference: 5) Hayashi H, et al: Genetic background of Japanese patients with adult-onset storage diseases in the liver. Hepatology Research 37: 777-783, 2007.
– reference: 3) Nagayoshi Y, et al: A Q312X mutation in the hemojuvelin gene is associated withcardiomyopathy due to juvenile haemochromatosis. European Journal of Heart Failure 10: 1001-1006, 2008.
– reference: 6) Hayashi H, et al: Genetic Background of Primary Iron Overload Syndromes in Japan. Internal Medicine 45 (20): 1107-1111, 2006.
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Snippet 29歳,男性.歩行中の意識消失発作にて救急搬送.来院時神経学的所見正常.心房細動,心機能低下に加え,血清フェリチン異常高値,肝酵素上昇を認めた.本例は13歳...
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StartPage 1069
SubjectTerms HJV遺伝子
デフェラシロクス
遺伝性ヘモクロマトーシス
Title 左室機能低下を来した遺伝性ヘモクロマトーシスの1例
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