scholarly journals Intracerebellar hematoma caused by posterior fossa dural arteriovenous malformation - A case report.

Nosotchu ◽  
1989 ◽  
Vol 11 (1) ◽  
pp. 26-31
Author(s):  
Toshiro Uno ◽  
Shuhji Niikawa ◽  
Hiroaki Nokura ◽  
Akio Ohkuma ◽  
Hiromu Yamada
Keyword(s):  
Case Report ◽  
Arteriovenous Malformation ◽  
Posterior Fossa ◽  
Dural Arteriovenous Malformation

scholarly journals Dural arteriovenous malformation in the posterior fossa - Case report.

1981 ◽  
Vol 28 (2) ◽  
pp. 147-151 ◽  
Author(s):  
MINORU SHIGEMORI ◽  
MORIHISA SHIRAHAMA ◽  
KUNITADA HARA ◽  
TAKASHI TOKUTOMI ◽  
TOMOYUKI KAWABA
Keyword(s):  
Case Report ◽  
Arteriovenous Malformation ◽  
Posterior Fossa ◽  
Dural Arteriovenous Malformation

Unusual Posterior Fossa Dural Arteriovenous Malformation in a Neonate: Case Report

Neurosurgery ◽  
1986 ◽  
Vol 19 (6) ◽  
pp. 1021-1024 ◽  
Author(s):  
Donald A. Ross ◽  
Joseph Walker ◽  
Michael S. B. Edwards
Keyword(s):  
Heart Failure ◽  
Congestive Heart Failure ◽  
Case Report ◽  
Arteriovenous Malformation ◽  
Posterior Fossa ◽  
Dural Arteriovenous Malformation ◽  
Intracranial Circulation

Abstract We report the case of an infant born with an unusual posterior fossa dural arteriovenous malformation that was supplied by the entire intracranial circulation. The lesion caused hydrocephalus and congestive heart failure that led to the infant's death.

Spontaneous regression of posterior fossa dural arteriovenous malformation

1979 ◽  
Vol 51 (5) ◽  
pp. 715-717 ◽  
Author(s):  
Shunro Endo ◽  
Keiji Koshu ◽  
Jiro Suzuki
Keyword(s):  
Arteriovenous Malformation ◽  
Posterior Fossa ◽  
Spontaneous Regression ◽  
Surgical Intervention ◽  
Clinical Symptoms ◽  
Dural Arteriovenous Malformation ◽  
Content Type ◽  
Homonymous Hemianopsia ◽  
Bleeding Episodes ◽  
Fine Print

✓ The authors report a case of infratentorial arteriovenous malformation that regressed spontaneously within 25 months without bleeding episodes or surgical intervention. The patient's clinical symptoms, left-sided tinnitus, cranial bruit, and right homonymous hemianopsia, disappeared completely over the same period.

scholarly journals Dural Arteriovenous Malformation in the Anterior Fossa. Case Report

1981 ◽  
Vol 21 (1) ◽  
pp. 131-134 ◽  
Author(s):  
Shoji BITOH ◽  
Hidemitsu NAKAGAWA ◽  
Norio ARITA ◽  
Masaaki FUJIWARA
Keyword(s):  
Case Report ◽  
Arteriovenous Malformation ◽  
Dural Arteriovenous Malformation ◽  
Anterior Fossa

Arteriovenous Malformation Associated with Multiple Aneurysms in the Posterior Fossa: A Case Report with a Review of the Literature

Neurosurgery ◽  
1987 ◽  
Vol 21 (3) ◽  
pp. 387-391 ◽  
Author(s):  
J. Noterman ◽  
P. Georges ◽  
J. Brotchi
Keyword(s):  
Case Report ◽  
Subarachnoid Hemorrhage ◽  
Arteriovenous Malformation ◽  
Posterior Fossa ◽  
The Other ◽  
Review Of The Literature ◽  
Multiple Aneurysms ◽  
One Stage ◽  
Cerebellar Artery

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.

Arteriovenous fistula around the ventriculoperitoneal shunt system in a patient with a dural arteriovenous malformation of the posterior fossa

1995 ◽  
Vol 82 (2) ◽  
pp. 288-290 ◽  
Author(s):  
Shin-ichi Yoshimura ◽  
Nobuo Hashimoto ◽  
Kiyoshi Kazekawa ◽  
Atsushi Obata ◽  
Chikao Yutani ◽  
...  
Keyword(s):  
Arteriovenous Malformation ◽  
Posterior Fossa ◽  
Ventriculoperitoneal Shunt ◽  
Rare Complication ◽  
Therapeutic Embolization ◽  
Dural Arteriovenous Malformation ◽  
Shunt System ◽  
Content Type ◽  
Underlying Mechanisms ◽  
Dural Avm

✓ A dural arteriovenous malformation (AVM) of the posterior fossa can produce persistent tinnitus, convulsions, and dementia. Successful therapeutic embolization may result in a complete cure, but in some cases, patients do not respond to the treatment. The authors report a patient with a dural AVM of the posterior fossa that did not respond to repeated intravascular treatments, but resulted in an arteriovenous shunt in the scalp around the ventriculoperitoneal shunt system. Although several hypotheses have been proposed on the pathogenesis of dural AVMs, the underlying mechanisms remain unknown. The rare complication we encountered may shed some light on the pathogenesis of dural AVMs.

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