Results 101 to 110 of about 613,500 (197)

Cavernous malformation of the trigeminal nerve [PDF]

, 2006
A cavernous malformation involving the Gasserian ganglion, 2nd and 3rd divisions of the trigeminal nerve on the left side was resected via an extradural route in a 54 year old male. Cavernous malformations of the cranial nerves are rare.
Romão,H., Magalhães,Z., Resende,M., Magalhães,F., Rocha Vaz,A., Honavar,M., Resende-Pereira,J., Mascarenhas,L.   +7 more
core   +1 more source

[Cerebral cavernous malformations].

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 2005
Cerebral cavernous malformations exist in sporadic and familial forms. They have considerable genetic and clinical heterogeneity. Better understanding of these disorders may improve management.This review is based on personal experience and recent literature.Cerebral cavernous malformations are venous malformations that can be detected with gradient ...
Jeanette, Koht, Geir J, Braathen, Dirk, Neubert, Michael Bjørn, Russell   +3 more
openaire   +1 more source

Chiasmal cavernous malformation. A rare cause of acute visual loss

, 2000
A rare cause of acute visual loss due to a chiasmal cavernous malformation is presented. Acute visual loss was due to local hemorrhage and volume expansion of the cavernous malformation inside and outside of the optic chiasma.

core  

Surgical Treatment of Cavernous Malformation of Pineal Region [PDF]

, 2017
The main causes of pineal apoplexy are hemorrhage associated with pineal region tumors, vascular malformations, and pineal cysts. Cavernous malformations rarely occur in the pineal region, with only fifteen cases reported previously.
김동석, 박용구, 최중언
core  

Unusual co-occurrence of hypertrophic inferior olivary degeneration with infratentorial cavernomatosis and orbital cavernous hemangioma

Radiology Case Reports
Hypertrophic olivary degeneration (HOD) is a rare condition resulting from a lesion in the Guillain-Mollaret triangle (GMT), causing transsynaptic degeneration and hypertrophy of the inferior olivary nucleus (ION).
Jihane EL Houssni, Salma Malak Ridah, Sanae Jellal, Meryem Edderai, Hassan EN Nouali, Jamal EL Fenni, Tarik Salaheddine   +6 more
doaj   +1 more source

Developing a Randomised Efficacy PREcision medicine Platform trial design for Cavernomas: the CARE PREP study

Efficacy and Mechanism Evaluation
Background Symptomatic cerebral cavernous malformations are a rare sporadic or familial disease, which may cause haemorrhagic strokes or epileptic seizures.
Rustam Al-Shahi Salman, Kasia Adamczuk, Richard A Parker, Christopher J Weir, Roberto Latini, Helen Kim, David White, Helen Evans, Jana Bergholtz, Cornelia Lee, Carlos Casaus   +10 more
doaj   +1 more source

Stereotactic radiosurgery for cerebral cavernous malformation: comparison of hemorrhage rates before and after stereotactic radiosurgery

Brain and Spine, 2021
B. Karaaslan, B. Gulsuna, G. Erol, Ö. Dağlı, Ö.H. Emmez, G. Kurt, E. Çeltikçi, A.Ö. Börcek   +7 more
doaj   +1 more source

Epidemiology and Aetiology of Cerebral Cavernous Malformations

Abstract Cerebral cavernous malformations (CCMs) are vascular anomalies affecting the central nervous system in up to 0.5% of the population. These lesions are characterised by thin-walled, dilated blood vessels that are susceptible to haemorrhage.
Hiroki, Hongo, Satoru, Miyawaki, Nobuhito, Saito   +2 more
openaire   +2 more sources

Editorial: Cerebral cavernous malformations

Frontiers in Neurology
Zuurbier, Susanna M., Santos, Alejandro N., Flemming, Kelly D., Lanzino, Giuseppe, Dammann, Philipp, Heldner, Mirjam R.   +5 more
openaire   +3 more sources

Spontaneous resolution of a Chiari malformation Type I and syrinx after supratentorial craniotomy for excision of a cavernous malformation

, 2012
The pathogenesis of Chiari malformation Type I (CM-I) and associated syringomyelia is incompletely understood. Patients often present in middle age with incidental or minimally symptomatic CM-I, whose management is controversial.
Schirmer, Clemens, MD
core   +1 more source