Meningioma Associated with Aneurysm and Subarachnoid Hemorrhage: Case Report and Review of the Literature

Neurosurgery ◽  
1987 ◽  
Vol 20 (1) ◽  
pp. 24-26 ◽  
Author(s):  
Gary M. Bloomgarden ◽  
Thomas N. Byrne ◽  
Dennis D. Spencer ◽  
Michael D. Heafner

Abstract A patient presented with spontaneous subarachnoid hemorrhage after a prolonged episode of coughing. A preoperative computed tomographic (CT) scan confirmed subarachnoid hemorrhage, but demonstrated no other lesion. Arteriography revealed an ophthalmic artery aneurysm. Operation revealed the aneurysm to be intracavernous without sign of prior rupture; however, a small hemorrhagic meningioma was removed from the ipsilateral anterior clinoid process. In this case, coincidental meningioma and aneurysm presented as a subarachnoid hemorrhage secondary to tumor hemorrhage. The follow-up of cases of subarachnoid hemorrhage with negative arteriography with sequential CT scans is discussed.

Neurosurgery ◽  
1986 ◽  
Vol 19 (6) ◽  
pp. 1016-1020 ◽  
Author(s):  
Walter A. Hall ◽  
Eduardo J. Yunis ◽  
Leland A. Albright

Abstract A 6-month-old girl had a gradually increasing head circumference. A preoperative computed tomographic (CT) scan of the head revealed an enhancing calcified partially cystic right frontal mass that was removed through a right frontotemporal craniotomy. On microscopic examination, the tumor was composed of sheets of neurons in a glial background alternating with highly cellular anaplastic areas. The diagnosis of anaplastic ganglioglioma was made. The child has done well for the 20 months since the operation without any evidence of tumor recurrence on subsequent CT scans. Because of the immaturity of the child's developing central nervous system, we have elected not to initiate radiotherapy at this time. The pertinent literature regarding gangliogliomas is reviewed.


2018 ◽  
Vol 24 (4) ◽  
pp. 383-386
Author(s):  
Nimer Adeeb ◽  
Justin Moore ◽  
Christoph J Griessenauer ◽  
Raghav Gupta ◽  
Ahad A Fazelat ◽  
...  

Introduction Ophthalmic segment aneurysms may present with visual symptoms due to direct compression of the optic nerve. Treatment of these aneurysms with the Pipeline embolization device (PED) often results in visual improvement. Flow diversion, however, has also been associated with occlusion of the ophthalmic artery and visual deficits in a small subset of cases. Case report A 49-year-old Caucasian female presented with subarachnoid hemorrhage due to a ruptured anterior communicating artery aneurysm. On follow-up imaging, the patient was found to have a right asymptomatic ophthalmic segment aneurysm. Due to the irregular shape of the aneurysm and history of aneurysmal subarachnoid hemorrhage, the decision was made to treat the aneurysm with a PED. Postoperatively, the patient complained of floaters in the right eye. Detailed ophthalmologic examination showed retinal hemorrhage and cotton-wool spots on the macula. Such complication after PED placement has never been reported in the literature. Conclusion Visual complications after PED placement for treatment of ophthalmic segment aneurysms are rare. It is thought that even in cases where the ophthalmic artery occludes, patients remain asymptomatic due to the rich collateral supply from the external carotid artery branches. Here we report a patient who developed an acute retinal hemorrhage after PED placement.


Neurosurgery ◽  
2003 ◽  
Vol 53 (3) ◽  
pp. 754-761 ◽  
Author(s):  
Christopher I. MacKay ◽  
Patrick P. Han ◽  
Felipe C. Albuquerque ◽  
Cameron G. McDougall

Abstract OBJECTIVE AND IMPORTANCE Dissecting aneurysms of the intracranial vertebral artery are increasingly recognized as a cause of subarachnoid hemorrhage. We present a case involving technical success of the stent-supported coil embolization but with recurrence of the dissecting pseudoaneurysm of the intracranial vertebral artery. The implications for the endovascular management of ruptured dissecting pseudoaneurysms of the intracranial vertebral artery are discussed. CLINICAL PRESENTATION A 36-year-old man with a remote history of head injury had recovered functionally to the point of independent living. He experienced the spontaneous onset of severe head and neck pain, which progressed rapidly to obtundation. A computed tomographic scan of the head revealed subarachnoid hemorrhage centered in the posterior fossa. The patient underwent cerebral angiography, which revealed dilation of the distal left vertebral artery consistent with a dissecting pseudoaneurysm. INTERVENTION Transfemoral access was achieved under general anesthesia, and two overlapping stents (3 mm in diameter and 14 mm long) were placed to cover the entire dissected segment. Follow-up angiography of the left vertebral artery showed the placement of the stents across the neck of the aneurysm; coil placement was satisfactory, with no residual aneurysm filling. Approximately 6 weeks after the patient's initial presentation, he developed the sudden onset of severe neck pain. A computed tomographic scan showed no subarachnoid hemorrhage, but computed tomographic angiography revealed that the previously treated left vertebral artery aneurysm had recurred. Angiography confirmed a recurrent pseudoaneurysm around the previously placed Guglielmi detachable coils. A test balloon occlusion was performed for 30 minutes. The patient's neurological examination was stable throughout the test occlusion period. Guglielmi detachable coil embolization of the left vertebral artery was then performed, sacrificing the artery at the level of the dissection. After the procedure was completed, no new neurological deficits occurred. On the second day after the procedure, the patient was discharged from the hospital. He was alert, oriented, and able to walk. CONCLUSION We appreciate the value of preserving a parent vessel when a dissecting pseudoaneurysm of the intracranial vertebral artery ruptures in patients with inadequate collateral blood flow, in patients with disease involving the contralateral vertebral artery, or in patients with both. However, our case represents a cautionary note that patients treated in this fashion require close clinical follow-up. We suggest that parent vessel occlusion be considered the first option for treatment in patients who will tolerate sacrifice of the parent vessel along its diseased segment. In the future, covered stent technology may resolve this dilemma for many of these patients.


2006 ◽  
Vol 58 (suppl_4) ◽  
pp. ONS-E379-ONS-E379 ◽  
Author(s):  
Vivek R. Deshmukh ◽  
Jeffrey Klopfenstein ◽  
Felipe C. Albuquerque ◽  
Louis J. Kim ◽  
Robert F. Spetzler

Abstract Objective and Importance: Distal coil migration is a rare but hazardous complication of aneurysm coil embolization. Various microsnare devices have been developed to address this problem. We describe the surgical management of a case in which microsnare retrieval failed. Clinical Presentation: A 34-year-old woman presented with subarachnoid hemorrhage. Magnetic resonance imaging, computed tomography angiography, and conventional angiography showed an approximately 2.5-mm ophthalmic artery aneurysm. Using balloon remodeling, a 2 × 4-cm coil was deployed into the aneurysm fundus. While the coil pusher was being removed after deployment, the microcatheter advanced abruptly into the aneurysm. The coil mass was dislodged and migrated into the angular branch of the middle cerebral artery. Contrast extravasation was noted during attempted retrieval with a microsnare device. Technique: Computed tomographic scans showed a subarachnoid hemorrhage in the territory of the left frontotemporal operculum. A left modified orbitozygomatic approach was performed. The coil mass was removed from the angular artery and a thromboembolectomy was performed. The artery was repaired and the pseudoaneurysm was clip ligated. The ophthalmic artery aneurysm was clip ligated. The patient recovered without deficits. Conclusion: Distal coil migration and arterial perforation can be treated surgically with a good clinical outcome.


Neurosurgery ◽  
1987 ◽  
Vol 21 (1) ◽  
pp. 86-89 ◽  
Author(s):  
Yoon S. Hahn ◽  
David G. McLone

Abstract A case of bilateral ophthalmic artery aneurysm of traumatic origin is discussed. The patient presented with progressive loss of vision, memory deficit, and expressive aphasia. A computed tomographic scan revealed enhancing lesions near the region of the optic chiasm. The diagnosis of cerebral aneurysm was confirmed by cerebral angiography. At operation, bilateral ophthalmic artery aneurysms were successfully clipped. (Neurosurgery 21: 86-89, 1987)


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