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Cerebral cavernous malformations and epilepsy [PDF]
Neurosurgical Focus, 2006 âś“Seizures and epilepsy are frequent clinical manifestations of cerebral cavernous malformations (CCMs) and represent the most common symptomatic presentation of supratentorial lesions. Clinicians often diagnose CCMs in patients after a first seizure, or in some cases after obtaining neuroimaging studies in patients suffering from chronic epilepsy ...
Issam, Awad, Pascal, Jabbour
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High Prevalence of Spinal Cord Cavernous Malformations in the Familial Cerebral Cavernous Malformations Type 1 Cohort [PDF]
, 2020 Background and purposeCavernous malformations occur most often in the brain but can occur in the spinal cord. Small studies of patients with familial cerebral cavernous malformations suggested a prevalence of spinal cord cavernous malformations of 20%-42%
Kim, H +9 more
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Cerebral cavernomatosis and epilepsy: treatment and serial imaging follow-up [PDF]
Romanian Journal of Neurology, 2023 Cerebral malformations, known as cavernomas, are low flow vascular malformations that have a multilobulated appearance. A large percent of cavernous malformations have seizures as initial symptoms.
Catalina Elena Bistriceanu +1 more
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Mitral valve plasty in a patient with multiple cerebral cavernous malformations: A case report
Clinical Case Reports, 2022 Cerebral cavernous malformations (CCMs) are blood vessel malformations, often untreated if asymptomatic. However, upon cardiac surgery with cardiopulmonary bypass, cerebral edema/hemorrhage may occur.
Shigeyuki Yamashita +6 more
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Rigid endoscopic surgery of brainstem cavernous malformation on the cerebral aqueduct. Case report
Ukrainian Neurosurgical Journal, 2021 Cavernous angiomas (malformations) of the brain occur in 0.5% of the population. Most of them are asymptomatic, but due to their anatomical features, namely escape of blood into surrounding tissues, significant neurological symptoms can occur.
Orest I. Palamar +4 more
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Asymptomatic Familial Multiple Cerebral Cavernous Malformation in a 73-Year-Old Woman
Case Reports in Radiology, 2021 Cerebral cavernous malformations (CCMs) are dilated blood vessels which can develop sporadically or in familial form and are the commonest malformations of blood vessels in the spinal cord and brain.
Klenam Dzefi-Tettey +4 more
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, 2019 Supplementary data in support of manuscript: "Stereotactic radiosurgery for cerebral cavernous malformations: a systematic review"
Poorthuis, Michiel, Rinkel, Leon
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Molecular genetic analysis of cerebral cavernous malformations: An update [PDF]
, 2021 Cerebral cavernous malformations (CCM) can occur either as sporadic or familial form with autosomal dominant inheritance. Three CCM genes have been identified: CCM1 (KRIT1), CCM2 (MGC4607), and CCM3 (PDCD10).
Riolo G., Battistini S., Ricci C.
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Journal of the Belgian Society of Radiology, 2014 Cerebral cavernous malformations, also known as cavernous angioma or cavernoma, are a type of vascular disorder. They consist of abnormally large vascular cavities or sinusoid channels of varying size. The majority of cavernous malformations in the brain
Dr M.R. Parizel +4 more
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The cerebral cavernous malformations proteins
Oncotarget, 2015 Inherited mutations in three genes lead to the familial form of Cerebral Cavernous Malformations (CCM). These vascular dysplasias most commonly occur in the brain, and manifest as dilated, mulberry-shaped lesions with a single endothelial layer. The consequences of these lesions can be leakage and sequelae such as focal neurological deficits, epilepsy,
Xiaofeng, Li +2 more
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