Despite the rarity of desmoplastic cerebral astrocytoma of infancy (DCAI),
it has distinct clinical and pathological features. The present case is a t
ypical DCAI except for its detection and operational age and intermingling
with pleomorphic glial cells. In this case, although a cystic lesion of the
right temporal lobe was noticed when the patient was 6 months old, it was
not regarded as a tumor and wasn't removed until he was 9 years old. It is
quite unusual that a DCAI was able to exist in the cerebrum for 9 years. Ho
wever, no metastasis occurred and distinct macroscopic and microscopic feat
ures of the tumor were not different from typical DCAI except for an interm
ingling with pleomorphic glial cells. Furthermore, even in the pleomorphic
areas, the absence of necrosis and an MIB-1 index of 2.9% indicated non-agg
ressive growth. These features of the present case may provide additional i
nformation as to the character of DCAI, which generally has a favorable pro
gnosis.