Results 11 to 20 of about 8,369 (198)

Dural based cavernoma of cerebral convexity – A rare case report

open access: yesInterdisciplinary Neurosurgery, 2023
Cerebral cavernous malformations occur in about 0.4–0.5 % of the population. They account for about 5–13 % of all vascular malformations of the central nervous system, commonly occurring in the cerebral parenchyma.
H. Mohamed Naleer   +6 more
doaj   +1 more source

A Chinese Family With Cerebral Cavernous Malformation Caused by a Frameshift Mutation of the CCM1 Gene: A Case Report and Review of the Literature

open access: yesFrontiers in Neurology, 2022
BackgroundFamilial cerebral cavernous malformation (FCCM) is a vascular malformation disease closely linked to three identified genes: KRIT1/CCM1, MGC4607/CCM2 and PDCD10/CCM3.
Wenyu Liu   +17 more
doaj   +1 more source

Diagnosis and treatment status of suprasellar optic pathway cavernous malformations

open access: yesJournal of International Medical Research, 2023
Cerebral cavernous malformations constitute a subtype of cerebral vascular malformation typically located in the cerebral cortex. However, their occurrence in the suprasellar optic pathway is relatively rare.
Songbai Xu, Liu Yang
doaj   +1 more source

Vertigo due to cerebellar cavernous malformation: A case report

open access: yesRadiology Case Reports, 2022
Central vertigo is a result of vestibular structure dysfunction in the central nervous system. Currently, misdiagnoses between peripheral and central lesions are frequent, and diagnostic testing costs are high.
Putri Maharani, MD   +2 more
doaj   +1 more source

Medical monitoring of patient with cavernous hemangioma of the retina and intracranial involvement

open access: yesAmerican Journal of Ophthalmology Case Reports, 2020
Purpose: To describe a case report of Cavernous Hemangioma of the Retina (CHR) and highlight the importance of investigating intracranial system when retinal vascular alterations are present.
Laís Yumi Sakano   +2 more
doaj   +1 more source

Genetically diagnosed Birt-Hogg-Dubé syndrome and familial cerebral cavernous malformations in the same individual: a case report. [PDF]

open access: yes, 2016
When faced with an unusual clinical feature in a patient with a Mendelian disorder, the clinician may entertain the possibilities of either the feature representing a novel manifestation of that disorder or the co-existence of a different inherited ...
Skytte, Anne-Bine   +2 more
core   +6 more sources

Signalling through cerebral cavernous malformation protein networks [PDF]

open access: yesOpen Biology, 2020
Cerebral cavernous malformations (CCMs) are neurovascular abnormalities characterized by thin, leaky blood vessels resulting in lesions that predispose to haemorrhages, stroke, epilepsy and focal neurological deficits.
Valerie L. Su, David A. Calderwood
doaj   +1 more source

Exceptional aggressiveness of cerebral cavernous malformation disease associated with PDCD10 mutations. [PDF]

open access: yes, 2015
PurposeThe phenotypic manifestations of cerebral cavernous malformation disease caused by rare PDCD10 mutations have not been systematically examined, and a mechanistic link to Rho kinase-mediated hyperpermeability, a potential therapeutic target, has ...
Akers, Amy L   +16 more
core   +2 more sources

A Case Report and Overview of Familial Cerebral Cavernous Malformation Pathogenesis in an Adult Patient [PDF]

open access: yes, 2018
OBJECTIVE We present a case of a 39 year-old woman who presented with a solitary cavernous malformation hemorrhage without any other lesions, and subsequently presented several months later with a new hemorrhage from a de novo lesion.
Arul, BS, Manu K.   +2 more
core   +2 more sources

Venous Malformations in Childhood: Clinical, Histopathological and Genetics Update

open access: yesDermatopathology, 2021
Our knowledge in vascular anomalies has grown tremendously in the past decade with the identification of key molecular pathways and genetic mutations that drive the development of vascular tumors and vascular malformations.
Isabel Colmenero, Nicole Knöpfel
doaj   +1 more source

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