No evidence of de novo amyloidosis in recipients of domino liver transplantation:: 12 to 40 (mean 24) month follow-up

被引:19
作者
Bittencourt, PL
Couto, CA
Leitao, RMC
Siqueira, SA
Farias, AQ
Massarollo, PCB
Mies, S
机构
[1] Univ Sao Paulo, Sch Med, Liver Unit, Sao Paulo, Brazil
[2] Univ Sao Paulo, Dept Pathol, Sch Med, BR-01426000 Sao Paulo, SP, Brazil
来源
AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS | 2002年 / 9卷 / 03期
关键词
domino liver transplantation; amyloidosis; familial amyloid polyneuropathy;
D O I
10.3109/13506120209114822
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Domino liver transplantation (DLT) has been performed for selected recipients at several centers, but de novo amyloidosis in recipients of livers from patients with familial amyloid polyneuropathy (FAP) remains a serious concern. Aim: To evaluate the occurrence of de novo amyloidosis in recipients of DLT. Patients and Methods: Seven recipients of FAP livers were followed for clinical and electroneuromyographic signs of FAP and also for de novo amyloid deposition in the gut. Results: No signs and symptoms of de novo FAP nor any evidence of amyloid deposits in the gut were observed in recipients of DLT after a mean follow-up of 24 [12-40] months. Conclusions: Signs and symptoms of FAP do not occur early in recipients of DLT. These livers could therefore be offered to patients suitable for conventional LT, particularly older subjects in whom the event of de novo amyloidosis would seem improbable.
引用
收藏
页码:194 / 196
页数:3
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