Renal Cell Carcinoma and Hepatocellular Carcinoma in a Patient with Wilson's Disease

  • Kitahata Shogo
    Gastroenterology Center, Ehime Prefectural Central Hospital, Japan
  • Michitaka Kojiro
    Department of Internal Medicine, Saiseikai Imabari Dai2 Hospital, Japan
  • Kinebuchi Miyuki
    First Department of Pathology, Sapporo Medical University, Japan
  • Matsuura Akihiro
    Research Integrity Office, Fujita Health University, Japan
  • Hiraoka Atsushi
    Gastroenterology Center, Ehime Prefectural Central Hospital, Japan
  • Ohama Hideko
    Gastroenterology Center, Ehime Prefectural Central Hospital, Japan
  • Yanagihara Emi
    Gastroenterology Center, Ehime Prefectural Central Hospital, Japan
  • Saneto Hironobu
    Gastroenterology Center, Ehime Prefectural Central Hospital, Japan
  • Izumoto Hirofumi
    Gastroenterology Center, Ehime Prefectural Central Hospital, Japan
  • Kawamura Tomoe
    Gastroenterology Center, Ehime Prefectural Central Hospital, Japan
  • Kuroda Taira
    Gastroenterology Center, Ehime Prefectural Central Hospital, Japan
  • Tada Fujimasa
    Gastroenterology Center, Ehime Prefectural Central Hospital, Japan
  • Miyata Hideki
    Gastroenterology Center, Ehime Prefectural Central Hospital, Japan
  • Ninomiya Tomoyuki
    Gastroenterology Center, Ehime Prefectural Central Hospital, Japan
  • Hiasa Yoichi
    Department of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Japan

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説明

<p>No reports of renal cancer in patients with Wilson's disease (WD) exist. We herein report a 37-year-old Japanese man diagnosed with WD who had been treated with d-penicillamine 9 years prior. Hepatocellular carcinoma had been diagnosed at 36 years old and treated with radiofrequency ablation therapy. One year later, renal cancer and recurrent hepatocellular carcinoma had developed. The hepatocellular carcinoma was treated after renal cancer surgical resection of a clear-cell-type renal cell carcinoma, with iron, rather than copper, deposited on the renal cancer cells. This patient harbored a novel mutation, p. Leu1395Terfs in ATP7B. </p>

収録刊行物

  • Internal Medicine

    Internal Medicine 63 (7), 963-968, 2024-04-01

    一般社団法人 日本内科学会

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