Idiopathic adulthood ductopenia

I. Nakano, Y. Fukuda, Y. Koyama, F. Urano, M. Yamada, Y. Katano, A. Marui, K. Imada, T. Hayakawa, M. Ito, Y. Yamashita, M. Imoto, Y. Nakanuma

研究成果: ジャーナルへの寄稿学術論文査読

5 被引用数 (Scopus)

抄録

In 1981, a 26 year old man occasionally demonstrated elevated serum transaminase concentrations. He had no history of medication, or a personal or family history of jaundice, except for prolonged physiological jaundice as a neonate. Serum hepatitis B surface antigen, hepatitis C virus antibody and anti-mitochondrial antibody were absent. A wedge biopsy specimen revealed ductular proliferation, mild inflammation of the portal area and disappearance of bile ducts from 80% of the portal tracts. Serial sections demonstrated a vanishing bile duct. Endoscopic retrograde choledochopancreatography, portography and arteriography demonstrated no abnormalities. In 1994, the patient died of hepatic failure following a 12 year observation period. He was subsequently diagnosed with idiopathic adulthood ductopenia on the basis of the criteria proposed by Ludwig.

本文言語英語
ページ(範囲)411-415
ページ数5
ジャーナルJournal of Gastroenterology and Hepatology (Australia)
11
4
DOI
出版ステータス出版済み - 1996
外部発表はい

All Science Journal Classification (ASJC) codes

  • 肝臓学
  • 消化器病学

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