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Liver transplantation for familial amyloidotic polyneuropathy in Australia
Authors:Nishino M  Tagaya N  Lynch S V  Steadman C  Balderson G A  Strong R W
Affiliation:(1) Queensland Liver Transplant Service, Princess Alexandra Hospital, Brisbane, Australia, AU;(2) Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Brisbane, Australia, AU;(3) Second Department of Surgery, Dokkyo Medical University, Tochigi, Japan, JP;(4) Department of Surgery, Kurume University School of Medicine, 67 Asahi-Machi, Kurume-City, Fukuoka 830-0011, Japan, JP
Abstract:Familial amyloidotic polyneuropathy type 1 (FAP-1) is a type of systemic amyloidosis caused by mutant transthyretin (mTTR) that is mainly produced in the liver. Most patients have progressive peripheral and autonomic neuropathy. Ten patients with FAP underwent orthotopic liver transplantation (OLT) at the Queensland Liver Transplant Service (Princess Alexandra Hospital, Brisbane, Australia). Nine patients are still alive, and one patient died of cardiac failure 10 days after OLT. Some symptoms of FAP were alleviated in some of the patients. OLT seems to be a worthwhile treatment for FAP, because it halts the progression of symptoms and achieves improvement in some patients. Received for publication on July 15, 1999; accepted on April 14, 2000
Keywords:: familial amyloidotic polyneuropathy  orthotopic liver transplantation  neuropathy
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