A previously well 16-month-old boy presented to Sydney Children's Hospital
with generalised seizures. There was no history of neurofibromatosis and no
family history. Imaging revealed a well-demarcated, frontal intracranial m
ass at the grey-white matter junction with surrounding oedema. At operation
, the tumour was adherent to the underlying brain on its deep aspect but su
perficially connected to the dura. There was an associated peritumoural cys
t. The tumour was biopsied for intra-operative frozen section opinion and e
xcised in its entirety. The specimen consisted of a 25 x 25 x 17 mm nodule
of firm cream tissue and separate fragments. Histologically, the tumour was
a meningioma with frequent mitoses, necrosis and brain invasion. Optimal t
reatment, in view of the recurrence risk, includes complete excision and po
stoperative irradiation. The latter was deferred because of the young age.
At follow-up at 26 months, the child was well and free of disease on MRI sc
an. Paediatric meningiomas are rare, with very few brain-invasive examples
in reported series. In infants and young children, few meningiomas have bee
n reported. There are several notable differences between meningiomas in ch
ildren and adults. This report illustrates these differences.