Yamamoto T, Maeda N, Kawasaki H
Second Department of Internal Medicine, Tottori University Faculty of Medicine, Yonago, Japan.
J Gastroenterol. 1995 Jun;30(3):393-7. doi: 10.1007/BF02347517.
We report a case of kappa-AL amyloidosis which rapidly developed hepatic failure in a 79-year-old Japanese female who was admitted to our hospital because of abdominal distension and loss of appetite. Laboratory examination revealed a marked deterioration of liver function with cholestasis and monoclonal gammapathy. At the time that the diagnosis of IgG-kappa type multiple myeloma was made, jaundice was advanced, with continuous gastrointestinal bleeding. The patient died of hepatic failure 2 weeks after admission. Needle biopsy of the liver revealed a diffuse, massive deposition of amyloid protein.
我们报告一例κ型淀粉样变性病例,该病例发生在一名79岁的日本女性身上,她因腹胀和食欲不振入住我院,迅速发展为肝功能衰竭。实验室检查显示肝功能显著恶化,伴有胆汁淤积和单克隆丙种球蛋白病。在诊断为IgG-κ型多发性骨髓瘤时,黄疸已进展,伴有持续的胃肠道出血。患者入院2周后死于肝功能衰竭。肝脏穿刺活检显示淀粉样蛋白弥漫性大量沉积。