Mesenteric Venous Thrombosis in Hereditary Protein C Deficiency with the Mutation at Arg169(CGG→TGG)

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概要

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• A 39-year-old man with no significant medical history was admitted to our hospital with severe abdominal pain and melena. Computed tomographic (CT) scans demonstrated superior mesenteric venous thrombosis. Although thrombolysis and anticoagulant therapy was started immediately, symptoms of strangulation ileus developed. Laparotomy was therefore performed and revealed necrotic stenosis of the ileum. The patient, his father and sisters showed low protein C levels. Direct sequencing analysis of their protein C gene revealed a heterozygous mutation at codon 169 corresponding to the cleavage site of the activation peptide, which was referred to as protein C Tochigi.(Internal Medicine 42: 110-116, 2003)

• 社団法人 日本内科学会の論文
• 2003-01-01

著者

• Komura Yasuo

  The Department Of Internal Medicine Minami Matsuyama Hospital

• Yamanouchi Jun

  The First Department Of Internal Medicine Ehime University School Of Medicine

• Tamai Masatake

  The Department Of Internal Medicine Minami Matsuyama Hospital

• Kumon Izumi

  The Department Of Internal Medicine Minami Matsuyama Hospital

• Hato Takaaki

  The First Department Of Internal Medicine Ehime University School Of Medicine

• Momoi Atsuko

  The Department Of Internal Medicine Minami Matsuyama Hospital

• Matsubara Jun

  The Department Of Surgery Minami Matsuyama Hospital

• Miyauchi Kagen

  The Department Of Radiology Minami Matsuyama Hospital

• Tarumi Yoshinao

  The Department Of Internal Medicine Minami Matsuyama Hospital

関連論文

• Mesenteric Venous Thrombosis in Hereditary Protein C Deficiency with the Mutation at Arg169(CGG→TGG)
• Mesenteric Venous Thrombosis in Hereditary Protein C Deficiency with the Mutation at Arg169(CGG→TGG)

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