Partial liver transplantation from living donors in familial amyloid polyneuropathy

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Abstract
Partial liver transplantation using a graft from a living donor (PLT) has been carried out for children with incurable hepatic disorders. We have extended this technique to 5 adult patients (4 female and 1 male) with familial amyloid polyneuropathy (FAP). All were proven to have a TTR Met30 mutation. Four of these 5 patients are alive 5 to 28 months after operation, and 3 patients with a shorter duration of illness (less than jive years) showed remarkable clinical improvement. Periodic nausea and vomiting ceased and other autonomic symptoms including orthostatic hypotension, abnormal bowel movements and dysuria were also improving soon after PLT. Somatic motor and sensory neuropathic symptoms tended to improve very gradually. on the other hand. further progression of FAP symptoms was observed in one severely disabled patient with a 7 year-history of this disease. One other patient with a similar condition died 3 months after PLT. The donors who consisted of 2 sisters and 3 husbands recovered without complications mid returned to their previous social lives 2 months after operation. Recently, it has been shown that liver transplantation corrects the metabolic abnormality in FAP and therefore liver transplantation has been widely accepted as a treatment for FAR Since cadaveric donors are seldom available in Japan, we started to perform PLT for FAP patients and have demonstrated good results. PLT can safely be done on adult patients and this treatment seems to be more effective for FAP patients at an early stage.