Aiba T, Tanaka R, Koike T et al (1995) Natural history of intracranial cavernous malformations. J Neurosurg. https://doi.org/10.3171/jns.1995.83.1.0056
Moriarity J, Clatterbuck R, Rigamonti D (1999) The natural history of cavernous malformations. Neurosurg Clin N Am 10(3):411–417
Article CAS PubMed Google Scholar
Gross BA, Du R (2015) Cerebral cavernous malformations: natural history and clinical management. Expert Rev Neurother. https://doi.org/10.1586/14737175.2015.1055323
Flemming KD, Graff-Radford J, Aakre J et al (2017) Population-based prevalence of cerebral cavernous malformations in older adults: Mayo clinic study of aging. JAMA Neurol. https://doi.org/10.1001/jamaneurol.2017.0439
Article PubMed PubMed Central Google Scholar
Flemming KD, Smith E, Marchuk D, Derry WB (2003) Familial Cerebral Cavernous Malformations. In: GeneReviews® [Internet]. https://www.ncbi.nlm.nih.gov/books/NBK1293/. Accessed 6 Oct 2024
Zabramski JM, Wascher TM, Spetzler RF et al (1994) The natural history of Familial cavernous malformations: results of an ongoing study. J Neurosurg 80:422–432. https://doi.org/10.3171/jns.1994.80.3.0422
Article CAS PubMed Google Scholar
Idiculla PS, Gurala D, Philipose J et al (2020) Cerebral cavernous malformations, developmental venous anomaly, and its coexistence: a review. Eur Neurol 83:360–368
Dammann P, Jabbarli R, Wittek P et al (2016) Solitary sporadic cerebral cavernous malformations: risk factors of first or recurrent symptomatic hemorrhage and associated functional impairment. World Neurosurg 91:73–80. https://doi.org/10.1016/j.wneu.2016.03.080
Dammann P, Wrede K, Zhu Y et al (2017) Correlation of the venous angioarchitecture of multiple cerebral cavernous malformations with familial or sporadic disease: a susceptibility-weighted imaging study with 7-Tesla MRI. J Neurosurg. https://doi.org/10.3171/2016.2.JNS152322
Yu T, Liu X, Lin X et al (2016) The relation between angioarchitectural factors of developmental venous anomaly and concomitant sporadic cavernous malformation. BMC Neurol. https://doi.org/10.1186/s12883-016-0691-3
Article PubMed PubMed Central Google Scholar
Kalani MYS, Zabramski JM, Martirosyan NL, Spetzler RF (2016) Developmental venous anomaly, capillary telangiectasia, cavernous malformation, and arteriovenous malformation: spectrum of a common pathological entity? Acta Neurochir (Wien). https://doi.org/10.1007/s00701-015-2675-2
Peyre M, Miyagishima D, Bielle F et al (2021) Somatic PIK3CA mutations in sporadic cerebral cavernous malformations. N Engl J Med 385:996–1004. https://doi.org/10.1056/NEJMoa2100440
Article CAS PubMed PubMed Central Google Scholar
Snellings DA, Girard R, Lightle R et al (2022) Developmental venous anomalies are a genetic primer for cerebral cavernous malformations. Nat Cardiovasc Res 1. https://doi.org/10.1038/s44161-022-00035-7
Ren J, Huang Y, Ren Y et al (2023) Somatic variants of MAP3K3 are sufficient to cause cerebral and spinal cord cavernous malformations. Brain. https://doi.org/10.1093/brain/awad104
Akers A, Al-Shahi Salman R, Awad IA et al (2017) Synopsis of guidelines for the clinical management of cerebral cavernous malformations: consensus recommendations based on systematic literature review by the Angioma Alliance scientific advisory board clinical experts panel. Clin Neurosurg 80:665–680. https://doi.org/10.1093/neuros/nyx091
Zhang S, Ma L, Wu C et al (2020) A rupture risk analysis of cerebral cavernous malformation associated with developmental venous anomaly using susceptibility-weighted imaging. Neuroradiology. https://doi.org/10.1007/s00234-019-02274-1
Meng G, Bai C, Yu T et al (2014) The association between cerebral developmental venous anomaly and concomitant cavernous malformation: an observational study using magnetic resonance imaging. BMC Neurol. https://doi.org/10.1186/1471-2377-14-50
Article PubMed PubMed Central Google Scholar
Cogswell PM, Pillai JJ, Lanzino G, Flemming KD (2023) Prevalence of developmental venous anomalies in association with sporadic cavernous malformations on 7T MRI. Am J Neuroradiol 44. https://doi.org/10.3174/ajnr.A8072
Brinjikji W, El-Masri AER, Wald JT et al (2017) Prevalence of cerebral cavernous malformations associated with developmental venous anomalies increases with age. Childs Nerv Syst. https://doi.org/10.1007/s00381-017-3484-0
Hong YJ, Chung TS, Suh SH et al (2010) The angioarchitectural factors of the cerebral developmental venous anomaly; can they be the causes of concurrent sporadic cavernous malformation? Neuroradiology. https://doi.org/10.1007/s00234-009-0640-6
García-Pérez D, Panero I, Lagares A, González P (2020) De Novo cavernous malformation associated with a Pre-existing developmental venous anomaly. Could Magnetic Resonance Findings Predict Evolution? Clin Neuroradiol 30
Kumar S, Lanzino G, Brinjikji W et al (2019) Infratentorial developmental venous abnormalities and inflammation increase odds of sporadic cavernous malformation. J Stroke Cerebrovasc Dis. https://doi.org/10.1016/j.jstrokecerebrovasdis.2019.02.025
Ren AA, Snellings DA, Su YS et al (2021) PIK3CA and CCM mutations fuel cavernomas through a cancer-like mechanism. Nature. https://doi.org/10.1038/s41586-021-03562-8
Article PubMed PubMed Central Google Scholar
Scerrati A, Mantovani G, Travaglini F et al (2023) Bleeding risk evaluation in cerebral cavernous malformation, the role of medications, and hemorrhagic factors: a case-control study. Neurosurg Focus. https://doi.org/10.3171/2023.7.FOCUS23355
Dammann P, Saban DV, Herten A et al (2021) Cerebral cavernous malformations: prevalence of cardiovascular comorbidities and allergic diseases compared to the normal population. Eur J Neurol. https://doi.org/10.1111/ene.14833
Girard R, Khanna O, Shenkar R et al (2016) Peripheral plasma vitamin D and non-HDL cholesterol reflect the severity of cerebral cavernous malformation disease. Biomark Med. https://doi.org/10.2217/bmm.15.118
Article PubMed PubMed Central Google Scholar
Flemming KD, Kumar S, Brown RD et al (2020) Cavernous malformation hemorrhagic presentation at diagnosis associated with low 25-hydroxy-vitamin D level. Cerebrovasc Dis 49. https://doi.org/10.1159/000507789
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