Cavernous Angioma with Olivary Hypertrophy and Contralateral Cerebellar Diaschisis.
نویسندگان
چکیده
منابع مشابه
Venous Angioma, Cavernous Angioma, and Hemorrhage
In this issue of AJNR, Wilms et al ( 1) add to the ongoing debate whether the venous angioma, more recently called developmental venous anomaly (2), can be symptomatic, whether it alone can bleed, or whether such hemorrhage occurs because of the concomitant occurrence of a cavernous angioma . This debate is not just semantic. It is essential to pathophysiologic understanding of a given lesion s...
متن کاملCavernous angioma associated with venous angioma--two case reports.
A 17-year-old male and a 28-year-old female presented with cavernous angioma and venous angioma colocated in the same region, and manifesting as convulsions. The cavernous angiomas were extirpated without damage to the venous angioma. No postoperative neurological deficits were observed. The patients have been free of convulsions without anticonvulsant medication for 2 years. Early extirpation ...
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Third ventricular cavernous angiomas are rare vascular malformations of the brain. We report an eight-year old boy with a rare third ventricular cavernous angioma that hemorrhaged presenting with symptoms of acute hydrocephalus. Computed Tomography (CT) and Magnetic Resonance Imaging (MRI) showed a heterogenous ill-defined, solid and cystic intraventricular mass in the third ventricle which was...
متن کاملFetal cavernous angioma--case report.
A neonate male who developed cavernous angioma was born with a severe intraventricular hemorrhage and intraparenchymal hemorrhage in the basal ganglia. magnetic resonance imaging revealed a large, non-enhanced hematoma that packed the lateral ventricle. Surgery on the 2nd day of life verified a cavernous angioma associated with minimal hemosiderin and gliosis. Fetal cavernous angiomas, unlike s...
متن کاملAcquired cerebellar cavernous angioma following childhood radiotherapy in a patient with neurofibromatosis type 1.
We report the unusual case of a patient with neurofibromatosis type I, who was irradiated 16 years previously for a mesencephalic glioma causing hydrocephalus, and who developed a cerebellar haemorrhage caused by a histologically confirmed cavernous angioma, that was invisible on several earlier MRI scans. The different hypotheses concerning the de novo formation of cavernous angiomas (venous o...
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ژورنال
عنوان ژورنال: Internal Medicine
سال: 1997
ISSN: 0918-2918,1349-7235
DOI: 10.2169/internalmedicine.36.504