The aim of our study was to compare the outcome of medical treatment vs.
liver transplantation in infants with
neonatal hemochromatosis (NH) referred to King's College Hospital from 1990-2002. We conducted a retrospective review of 19 children from 14 families. Fifteen children presented at birth and 4 during the first week of life. One child was diagnosed by cordocentesis at 30 weeks of gestation. NH recurred in 7 of 9 families with further children. In one family, 2 children from different fathers were affected. All patients had elevated
ferritin levels,
hypoalbuminemia, and coagulopathy. Liver histology showed parenchymal collapse, diffuse
fibrosis, and moderate to severe hepatocyte
hemosiderin deposition. Extrahepatic
siderosis was demonstrated by magnetic resonance in 2 patients, lip biopsy in 3, and autopsy in 10. Ten patients received a chelation-
antioxidant cocktail: 1 survived, 4 died, and 5 required
liver transplantation, of whom 2 died. One of the 9 infants who did not receive the cocktail survived with medical support, 3 died, and 5 required
transplantation, of whom 3 died. Seven children are alive, 5 after
transplantation, at a median follow-up of 5.6 years, with excellent quality of life and no recurrence of the disease. In conclusion, chelation-
antioxidant treatment does not appear to modify the prognosis of NH, at least in severe cases.
Liver transplantation, with 50% long-term survival, remains the treatment of choice and should be promptly offered to those infants who do not improve with supportive medical treatment.