CAVERNOUS ANCIOMAS OF the dura mater are clinically and radiographical
ly distinct from parenchymal cavernous angiomas. In this report, we pr
esent two cases of dural cavernous angiomas located outside the middle
cranial fossa. The first patient is a 36-year-old woman with two dura
l cavernous angiomas, including one that enlarged during a 2-year peri
od of observation. The second patient is a 33-year-old man with medica
lly intractable seizures from a dural cavernous angioma of the convexi
ty, which was discovered at autopsy. From our experience and a review
of the literature, we have identified two groups of dural cavernous an
giomas that differ in incidence, natural history, and surgical managem
ent. Most dural cavernous angiomas arise from the middle fossa; in con
trast, only 15 cases of dural cavernous angiomas outside the middle fo
ssa have been reported. Those in the middle fossa are more clinically
aggressive and more difficult to resect surgically, because they grow
toward the cavernous sinus and the parasellar region. Most patients wi
th dural cavernous angiomas outside the middle fossa present with head
aches, whereas those patients with dural cavernous angiomas in the mid
dle fossa present with ocular signs, visual field defects, endocrinopa
thy, and trigeminal symptoms. Radiographically, both of the angiomas r
esemble meningiomas. Because of their intimate association with the ca
vernous sinus, surgical resection of middle fossa cavernous angiomas o
ften is incomplete and may require postoperative radiosurgery to contr
ol growth. In contrast, angiomas in other locations are easily and suc
cessfully resected with little blood loss, The location of dural caver
nous angiomas is an important factor in making the surgical decision a
nd in predicting the outcome.