| Literature DB >> 7647907 |
T Yamamoto1, N Maeda, H Kawasaki.
Abstract
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.Entities:
Mesh:
Year: 1995 PMID: 7647907 DOI: 10.1007/bf02347517
Source DB: PubMed Journal: J Gastroenterol ISSN: 0944-1174 Impact factor: 7.527