Ganglioneuroblastomas are tumors of sympathetic cell origin that conta
in both primitive neuroblastomalous and mature ganglioneuromatous elem
ents. It is thought that these tumors arise from a single cellular clo
ne and that the morphologically distinct components of ganglioneurobla
stomas represent cells in different stages of differentiation. Two pat
hologic variants of this tumor, composite and diffuse, have been descr
ibed; metastasis is more commonly seen with composite ganglioneuroblas
tomas. We analyzed a composite ganglioneuroblastoma for N-myc copy num
ber at initial resection and 2 years later after progressive disease.
In the second sample the more differentiated portion of the tumor was
analyzed separately from the neuroblastic foci for N-myc copy number a
nd DNA ploidy. The DNA content and N-myc copy number differed in the t
wo morphologically discrete areas of the tumor, suggesting that at lea
st two clones were present. More composite ganglioneuroblastomas need
to examined to determine whether these tumors are largely composed of
tumor cell populations with molecular heterogeneity.