Estimates of the incidence and outcome of tumours in neonates are unce
rtain and most reports relate to selected experience in single centres
. The definition of neonatal tumour is also unclear and histology is n
ot always an accurate predictor of outcome. This report documents the
incidence, clinical features, and outcome of neonatal tumours (birth-3
months) in a population-based paediatric register over a 30-year peri
od from 1960-89. Case note and pathology review identified 170 cases f
or analysis, of which 21 were leukaemias, 14 CNS tumours, and 135 soli
d tumours of differing types. Fifty-eight percent were diagnosed in th
e first month and mature teratoma was the most common diagnosis (29%).
Overall incidence increased over the period of the study. Important f
amily medical history was identified in 16% of cases and 15% of patien
ts had associated congenital abnormalities. Overall survival at 1 year
was 55%, with leukaemia having the poorest prognosis. Treatment strat
egies must be individualised but many patients may have a better progn
osis than expected and would benefit from assessment at a designated p
aediatric oncology centre. (C) 1994 Wiley-Liss, Inc.