Pleomorphic xanthoastrocytoma (PXA) is a well-described astrocytic neoplasm
with distinctive clinical and pathological features. Although most patient
s with PXAs are cured by surgical excision, other patients experience malig
nant progression and tumor recurrence. We describe a 47-year-old woman with
a left temporal lobe PXA that had classic histopathological characteristic
s as well as extensive clear cell and focal papillary changes, and some ana
plastic findings. The patient has now suffered two recurrences after comple
te resection. The case illustrates a rare, previously undescribed histologi
cal variant of PXA, with a prominent clear cell and focal papillary morphol
ogy. The study of histologically similar cases is needed to determine wheth
er this variant is always associated with a greater likelihood of recurrenc
e.