TY - JOUR
T1 - Liver transplantation for neurologic Wilson's Disease
T2 - Reflections on two cases within a Mexican cohort
AU - Duarte-Rojo, A.
AU - Zepeda-Gómez, S.
AU - García-Leiva, J.
AU - Remes-Troche, J. M.
AU - Ángeles-Ángeles, A.
AU - Torre-Delgadillo, A.
AU - Olivera-Martínez, M. A.
PY - 2009/7
Y1 - 2009/7
N2 - Background: Liver transplantation (LT) in Wilson's disease (WD) is mostly indicated when progressing liver disease or acute liver failure occurs. In patients with neurological manifestations, this procedure has not gained wide acceptance based on previous reports of dismal prognosis. Objective: To describe a Mexican cohort of patients with WD with special focus on LT in patients with deteriorating neurological manifestations. Material and Methods: Patients with confirmed WD and their first-degree relatives were evaluated at the hepatology clinic of a tertiary referral hospital. Attention was placed on therapy and outcome. Results: Eleven patients were followed for a period of up to 80 months (7 probands and 4 affected family members), 10 patients having hepatic manifestations and 4 having neuro psychiatric phenomena. Pharmacologic treatment was uniform in most patients, and LT was indicated in 2 cases because of deteriorating neurological status. These patients had total remission of their neurological manifestations with marked improvement on imaging studies. Conclusions: Follow-up and pharmacologic treatment was flawed by several adverse conditions present in our population. Patients with progressing neurological disease had a favorable outcome after LT, a similar response to the one reported by several authors. In conclusion, LT should be strongly considered for the treatment of these patients.
AB - Background: Liver transplantation (LT) in Wilson's disease (WD) is mostly indicated when progressing liver disease or acute liver failure occurs. In patients with neurological manifestations, this procedure has not gained wide acceptance based on previous reports of dismal prognosis. Objective: To describe a Mexican cohort of patients with WD with special focus on LT in patients with deteriorating neurological manifestations. Material and Methods: Patients with confirmed WD and their first-degree relatives were evaluated at the hepatology clinic of a tertiary referral hospital. Attention was placed on therapy and outcome. Results: Eleven patients were followed for a period of up to 80 months (7 probands and 4 affected family members), 10 patients having hepatic manifestations and 4 having neuro psychiatric phenomena. Pharmacologic treatment was uniform in most patients, and LT was indicated in 2 cases because of deteriorating neurological status. These patients had total remission of their neurological manifestations with marked improvement on imaging studies. Conclusions: Follow-up and pharmacologic treatment was flawed by several adverse conditions present in our population. Patients with progressing neurological disease had a favorable outcome after LT, a similar response to the one reported by several authors. In conclusion, LT should be strongly considered for the treatment of these patients.
KW - ATP7B gene
KW - Decoppering treatment
KW - Hepatolenticular degeneration
KW - Kayser-Fleischer ring
KW - México
KW - Orthotopic liver transplantation
UR - http://www.scopus.com/inward/record.url?scp=77953237937&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=77953237937&partnerID=8YFLogxK
M3 - Review article
C2 - 19858010
AN - SCOPUS:77953237937
SN - 0375-0906
VL - 74
SP - 218
EP - 223
JO - Revista de Gastroenterologia de Mexico
JF - Revista de Gastroenterologia de Mexico
IS - 3
ER -