scholarly journals Spontaneous subarachnoid hemorrhage due to arteriovenous malformation mimicking migraine: A case report

2022 ◽  
Vol 17 (3) ◽  
pp. 790-793
Author(s):  
Al Rasyid ◽  
Taufik Mesiano ◽  
Mohammad Kurniawan ◽  
Rakhmad Hidayat ◽  
Rahmad Mulyadi ◽  
...  
Neurosurgery ◽  
1987 ◽  
Vol 21 (3) ◽  
pp. 387-391 ◽  
Author(s):  
J. Noterman ◽  
P. Georges ◽  
J. Brotchi

Abstract The association of two aneurysms on the distal posteroinferior cerebellar artery with an arteriovenous malformation fed by the same artery is reported. A one-stage operation was performed. The other cases in the literature are analyzed with particular regard to the origin of the subarachnoid hemorrhage and the location of the aneurysms.


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 (1) ◽  
pp. 125-128 ◽  
Author(s):  
Juan F. Martinez-Lage ◽  
Máximo Poza ◽  
Juan A. Esteban ◽  
Joaquin Sola

Abstract The authors report a case of a ventricular oligodendroglioma associated with a cortical arteriovenous malformation. The patient presented with subarachnoid hemorrhage. Computed tomographic scan showed an intraventricular hyperdense lesion, mimicking a hematoma. Angiography revealed a superficial arteriovenous malformation in the right parietal lobe, unrelated to ventricular cavities. Both lesions were treated during the same operation. The diagnostic difficulties and the significance of this uncommon association are discussed.


Neurosurgery ◽  
2005 ◽  
Vol 56 (6) ◽  
pp. E1382-E1382 ◽  
Author(s):  
Soichi Oya ◽  
Toru Matsui ◽  
Akio Asai

Abstract OBJECTIVE AND IMPORTANCE: Arteriovenous malformations in the cranial nerves are very rare, and only one case has been reported in the literature. To our knowledge, this is the first case report of an arteriovenous malformation in the auditory nerve. CLINICAL PRESENTATION: A 30-year-old woman presented with a subarachnoid hemorrhage resulting from rupture of an arteriovenous malformation in the auditory nerve. INTERVENTION: During the operation, the auditory nerve bundle was found to be severely damaged and a nidus was identified inside the bundle. CONCLUSION: Although arteriovenous malformations are thought to arise in the 4th to 8th weeks of gestation, this case might indicate a more specific time of emergence based on embryogenesis of the cranial nerves.


Neurosurgery ◽  
1988 ◽  
Vol 22 (3) ◽  
pp. 558-560 ◽  
Author(s):  
Yasunobu Goto ◽  
Yoshinari Kamijyo ◽  
Yasuhiro Yonekawa ◽  
Haruhiko Kikuchi

Abstract A case of aneurysm of the posterior spinal artery of the upper cervical spinal cord is presented. The patient had severe intracranial subarachnoid hemorrhage with disturbance of consciousness. Four-vessel angiograms showed neither anomalous arrangement of the arteries nor arteriovenous malformation intracranially or in the spinal subarachnoid space. Operation disclosed a thrombosed aneurysm of the posterior spinal artery, which was radically excised and histologically examined. (Neurosurgery 22:558-560, 1988)


Neurosurgery ◽  
1986 ◽  
Vol 19 (4) ◽  
pp. 637-640 ◽  
Author(s):  
Michael K. Morgan ◽  
Raymond Chaseling ◽  
Ian Johnston ◽  
M. de Silva

Abstract A newborn with paraplegia and evidence of a subarachnoid hemorrhage was found to have a spinal arteriovenous malformation. The arteriovenous malformation was managed by direct surgical obliteration. This patient is the youngest ever reported to have this disorder and the youngest so treated.


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