Neuroblastoma (NB) is the most frequent solid tumour in early childhoo
d. NBs are extremely heterogeneous in terms of their biological charac
teristics and the clinical behaviour which ranges from lethal disease
to spontaneous regression and/or differentiation. Genetically, the het
erogeneity of these rumours is reflected mainly by differences in the
DNA content, presence of chromosome Ip deletions and amplification of
the proto-oncogene N-myc. Up to now, only the prognostic impact of N-m
yc amplification, based on a large series of analysed tumour samples,
was established and is now used as the discriminating factor for treat
ment stratification in a newly developed European protocol. The influe
nce of other genetic aberrations, i.e. dellp36, t(1;17), ploidy and ex
pression of certain proteins, such as nerve growth factor (NGF) recept
or proteins and CD44, on the biological behaviour were studied only in
a limited number of cases. We will review the literature and outline
our own observations dealing with the peculiar phenomena observed in s
ome NBs, i.e. spontaneous regression and/or maturation.