Results 111 to 120 of about 5,748 (167)
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Neurosurgical Review, 2010
Cystic cavernous angiomas are rarely found in patients. We have reviewed 25 cases of cystic cavernous angiomas, including our case. The patients were predominantly women (15 women and 10 men). The patients' ages ranged from 4 months to 75 years (mean age, 44.0 years).
Shigeo, Ohba +4 more
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Cystic cavernous angiomas are rarely found in patients. We have reviewed 25 cases of cystic cavernous angiomas, including our case. The patients were predominantly women (15 women and 10 men). The patients' ages ranged from 4 months to 75 years (mean age, 44.0 years).
Shigeo, Ohba +4 more
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Intramedullary cavernous angiomas
Surgical Neurology, 1989Two cases of histologically verified intramedullary cavernous angiomas at C3 and D5-6 are presented. Both patients suffered progressive myelopathy with intermittent improvement. In both cases preoperative diagnosis was possible by means of magnetic resonance imaging using spin echo techniques, fast imaging, and phase display, while spinal angiography ...
J, Zentner +3 more
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Intracranial cavernous angioma
Neurosurgical Review, 1992We report 14 cases of intracranial cavernous angioma, analyzing the clinical features, with special reference to the risk of bleeding, radiological images and treatment in these and in 153 published cases, 167 in all. Cerebral hemorrhage occurred in 44%: typical (intraparenchymal or subarachnoid) in 24.6%, and masked by epilepsy, headache or ...
L, Ferrante +5 more
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Intracerebral cavernous angiomas
Neurology, 1988We studied 31 patients with histologically verified intracerebral cavernous angiomas. Twenty-two patients were symptomatic; nine were asymptomatic. All 22 symptomatic patients had seizures, three had intracranial hemorrhage, and one had signs of a space-occupying lesion.
J P, Farmer +5 more
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Genetics of cavernous angiomas
The Lancet Neurology, 2007Cerebral cavernous malformations (CCM) are vascular malformations that can occur as a sporadic or a familial autosomal dominant disorder. Clinical and cerebral MRI data on large series of patients with a genetic form of the disease are now available. In addition, three CCM genes have been identified: CCM1/KRIT1, CCM2/MGC4607, and CCM3/PDCD10.
Pierre, Labauge +3 more
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Archives of Neurology, 1978
Cavernous angiomas are rare, surgically remediable vascular malformations of the CNS that may be characterized by hemorrhage, seizures, or focal neurologic deficits. Three families with cavernous angiomas have been described, and we report two more. In the first, the mother died suddenly with headache.
J M, Bicknell +4 more
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Cavernous angiomas are rare, surgically remediable vascular malformations of the CNS that may be characterized by hemorrhage, seizures, or focal neurologic deficits. Three families with cavernous angiomas have been described, and we report two more. In the first, the mother died suddenly with headache.
J M, Bicknell +4 more
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Intracranial cavernous angioma
American Journal of Roentgenology, 1977Cavernous angiomas are a rare but important clinical entity because of their potential curability. Three patients who had intracranial cavernous angiomas confirmed at surgery are presented. Preoperative recognition is greatly aided by a tendency to calcify, as identified both by skull films and more sensitively by computed tomography. A well demarcated
J E, Bartlett, P R, Kishore
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Cavernous Angiomas of the Skull
min - Minimally Invasive Neurosurgery, 1978The authors present a series of 25 cases of haemangioma of the skull and review the literature. Frontal localization was the most frequent, contrary to the data in the literature which suggest predominance in the parietal region. The reported predominance of females has not been confirmed. In the present series the relation of males to females was 17:8.
D, Kirchhoff, H R, Eggert, A L, Agnoli
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Cavernous Angioma of the Cavernous Sinus: Case Report
Neurosurgery, 1990Abstract An unusual case of cavernous angioma in the cavernous sinus (“cavernous cavernoma”) is presented. The acute onset of symptoms simulated Tolosa-Hunt syndrome, and after neuroradiological investigations, the suspected diagnosis was an intracavernous meningioma.
A, Sepehrnia +4 more
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The growth of cerebral cavernous angiomas
Neurosurgery, 1989Abstract The natural history of cavernous angiomas is poorly understood, and their growth has rarely been documented. We report three cases of cavernous angiomas that grew to large size in 6 years, 2 years, and 2 months, respectively.
E, Pozzati +3 more
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