Portopulmonary Hypertension Associated with Congenital Absence of the Portal Vein Treated with Bosentan
スポンサーリンク
概要
- 論文の詳細を見る
Portopulmonary hypertension (PPHTN) is pulmonary arterial hypertension (PAH) associated with portal hypertension. It is a common condition among liver transplantation candidates; however, its association with congenital absence of the portal vein (CAPV) has not yet been established. CAPV is a very rare developmental anomaly, which is usually accompanied by abnormal mesenteric drainage that bypasses the liver. Here, we report a rare case of severe PPHTN secondary to CAPV.
- 社団法人 日本内科学会の論文
著者
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Yoshida Kiyoshi
Department Of Internal Medicine Osaka City General Hospital
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Okura Hiroyuki
Department Of Cardiology Kawasaki Medical School
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Kawamoto Takahiro
Department of Cardiology, Kawasaki Medical School Hospital
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Neishi Yoji
Department of Cardiology, Kawasaki Medical School Hospital
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WATANABE Nozomi
Department of Cardiology, Kawasaki Medical School
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OBASE Kikuko
Department of Cardiology, Kawasaki Medical School
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HAYASHIDA Akihiro
Department of Cardiology, Kawasaki Medical School
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Obase Kikuko
Department Of Cardiology Kawasaki Medical School
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Watanabe Nozomi
Department Of Cardiology Kawasaki Medical School
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Watanabe Nozomi
川崎医科大学 循環器内科学
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OKAHASHI Noriko
Department of Cardiology Kawasaki Medical School
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Hino Tomoko
Postgraduate Clinical Training Center, Kawasaki Medical School Hospital
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Wada Nozomi
Department of Cardiology, Kawasaki Medical School Hospital
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Yoshida Kiyoshi
Department Of Applied Chemistry And Biotechnology Faculty Of Engineering Fukui University
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Hayashida Akihiro
Department Of Cardiology Kawasaki Medical School
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Kawamoto Takahiro
Department Of Cardiology Kawasaki Medical School
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Neishi Yoji
Department Of Cardiology Kawasaki Medical School
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Watanabe Nozomi
Department of Cardiology, Kawasaki Medical School Hospital
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Hayashida Akihiro
Department of Cardiology, Kawasaki Medical School Hospital
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Obase Kikuko
Department of Cardiology, Kawasaki Medical School Hospital
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