Familial amyloid polyneuropathy is an autosomal dominant disorder in w
hich the liver produces a variant prealbumin that is deposited along n
erves, leading to a progressive and fatal polyneuropathy that begins i
n the third decade of life. Liver transplantation has been the only su
ccessful treatment to date. Apart from the production of the variant p
rotein, there are no other abnormalities in these amyloid livers. We d
escribe two cases in which, at the time of transplantation, the amyloi
d livers were subsequently used for transplantation in another patient
, and we discuss the implications. Copyright (C) 1998 by the American
Association for the Study of Liver Diseases.