The cavernous angioma, also known as the cavernous malformation or cavernoma, is one of the vascular malformations characterized by the presence of sinusoid-like capillary vessels containing blood in very sluggish circulation (1). Intracranial cavernous angiomas are mostly parenchymal lesions and extra-axial cavernous angiomas are relatively rare, accounting for only 0.4 to 2% of all intracranial vascular malformations (2). Extra-axial cavernous angiomas usually arise in relation to the dura mater intracranially or at the spinal level and often mimick meningiomas. Most of these lesions have been found in the middle fossa at the level of cavernous sinus and they are rarely found in other dural locations outside the middle fossa. Other dural locations include the tentorium, the convexity, the anterior cranial fossa, Meckel's cave, the cerebellopontine angle, the sellar turcica, internal auditory canal, and cranial nerves (2-4). Only 3 cases of cavernous angiomas originated from the falx cerebri have been reported in the literature (3, 5, 6). We report a case of cavernous angioma occured in the falx cerebri with the neuroradiologic features, which is the fourth case to our knowledge.

A 22-yr-old female patient presented with an episode of generalized tonic-clonic type seizure. She had no focal neurologic deficit.

Histopathologically, intracerebral and extra-axial cavernous angiomas seem to be identical lesions. Cavernous angiomas consist of abnormally dilated, thin-walled vascular channels with walls composed of collagen lined by a layer of endothelium. Surrounding brain parenchyma is often gliotic and hemosiderin-stained and the lesions may contain feeding arteries and draining veins of slow flow. It can vary from a small petechial lesion of a few millimeters to a larger, wellcircumscribed, "mulberry-like" hemorrhagic mass of many centimeters in size (1, 2, 7, 8).

Intracranial cavernous angiomas are generally found in middle- aged women (3), though its cause is uncertain. Previously reported 3 cases of cavernous angiomas of falx cerebri were found in 47, 62, and 63-yr old women (3, 5, 6), respectively.

Though there is no specific neuroradiologic finding for extra-axial cavernous angiomas, the MRI pattern was known to reflect the histological appearance (7). The most common form of MRI findings such as speckled mixed intensity may reflect vascular lumens, their thromboses, and calcifications in the lesion. Intra-axial cavernous angiomas usually have a multifocal hyperintense center surrounded by a hypointense rim which results from the blood products in different stages of evolution (1, 9-11). However, the characteristic peripheral low-signal rim is usually absent in extra-axial cavernous angiomas, and this was true in our case. Extra-axial cavernous angiomas also have been reported as a soft mass often with a pseudocapsule that is formed by the dura mater, mimicking meningiomas.

Guermazi et al. (12) demonstrated that dural tail sign could be rarely seen in cavernous angioma from the dura in the cerebral convexity, and differential diagnosis from meningioma is even more difficult to eliminate when the dural cavernous angioma shows a dural tail. In our case, dural tail sign and calcifications were very prominent (3, 13).

In intracranial cavernous angioma, angiography usually reveals the flecked lesion stain at middle arterial to late venous phases due to slow blood flow, delayed stain, or an avascular mass. The sunburst of vessels radiating outwards from the central vascular pedicle, a typical finding of meningiomas, was reported that it was not found in cavernous angioma (3, 6, 8). Only an avascular mass effect was present in our case.

Little is known about the role of Thallium²⁰¹ SPECT in the diagnosis of cavernous angioma. Seo et al. (14) reported that Thallium²⁰¹ SPECT is useful in diagnosis of cavernous sinus hemangioma, presenting low uptake within the tumor in contrast to meningioma or malignant tumors which present high uptake due to increased tumor viability or tumor blood flow. The uptake of Thallium²⁰¹ within the brain is associated with tumor viability and tumor blood flow, and is much higher within meningiomas than malignant tumors. In this case, no definite abnormal Thallium²⁰¹ accumulation was observed, as same as the result of Seo's study.

In relation to the surgery of cavernous angioma at the cavernous sinus, bleeding was reported to be a major problem and preoperative differential diagnosis of extra-axial cavernous angioma from meningioma may be most important. However, little blood loss was reported in the surgery of cavernous angiomas of the falx cerebri (6). In our case, blood loss was only a little, and total removal was achieved without difficulty. No adjuvant therapy was required during the followup period.

We reported a very rare case of cavernous angioma that occured in the falx cerebri which was successfully removed, with special interest on its neuroradiologic features.