Results 151 to 160 of about 21,647 (203)
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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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Putaminal cavernous angioma presenting with hemichorea
Movement Disorders, 2004 We report on a 63-year-old man presenting with hemichorea on his right side. Magnetic resonance imaging revealed a left putaminal cavernoma. To our knowledge this is the first report of such a case caused by contralateral putaminal cavernous angioma. (C)
Berril Donmez +7 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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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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Cavernous Angioma of the Cerebral Aqueduct
World Neurosurgery, 2017Among the rare intraventricular cavernomas, purely intra-aqueductal cavernomas are exceptionally rare.A 62-year-old patient presented with progressive headache, memory loss, gait instability, and urinary incontinence. Magnetic resonance imaging showed the presence of a mass lesion located in the lumen of the cerebral aqueduct, associated with ...
Feletti A, Dimitriadis S, Pavesi G
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Intracranial cavernous angioma in the dura
Neurosurgery, 1989Abstract Cavernous malformations located in the dura are rare. We present a case of a large cavernous malformation located in the anterior fossa and implanted in the dura of a pregnant woman. It showed great vascularization on an angiogram, and resembled a meningioma on computed tomographic scan.
A, Isla +5 more
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Intrasellar cavernous angioma in neurofibromatosis
Human Pathology, 1991A case of neurofibromatosis complicated by a large intrasellar (pituitary) cavernous angioma is reported. Vascular abnormalities, consisting of smooth muscle cell proliferation in the intima of the intermediate and small arteries, were also observed in branches of the renal and pulmonary arteries.
Yasunori Nagata, Takehiro Mitsuhashi
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