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  • 11
    Electronic Resource
    Electronic Resource
    Springer
    Neuroradiology 29 (1987), S. 437-443 
    ISSN: 1432-1920
    Keywords: Tuberous sclerosis ; Brain, MRI studies ; Brain, CT studies ; Giant aneurysm
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The authors present four cases of tuberous sclerosis examined with MRI. The patho-anatomic aspects are reviewed and analysed with respect to MRI data. MRI appears superior to the CT particularly for imaging of cortical tubers, cystic lesions, and heterotopic clusters; these last two features were never described with MRI before. Here is also presented the second progressive case of giant intracranial aneurysm associated with tuberous sclerosis.
    Type of Medium: Electronic Resource
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  • 12
    ISSN: 1432-1920
    Keywords: Key words Temporal lobe epilepsy ; Hippocampal sclerosis ; Magnetic resonance imaging
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract MRI was performed in 222 consecutive adult patients with temporal lobe epilepsy of varying severity from January 1991 to May 1993. The diagnosis of hippocampal sclerosis was established visually by three independent observers. The accuracy of visual assessment of hippocampal asymmetry was compared with volumetric measurements. Neuropathological correlations were obtained in 63 patients with refractory seizures. Temporal lobe abnormalities were observed in 180 patients (81 %) as follows: hippocampal sclerosis in 122 (55 %); developmental abnormalities in 16 (7.2 %); tumours in 15 (6.8 %); scars in 11 (5 %); cavernous angiomas in 10 (4.5 %); miscellaneous lesions in 6. MRI was normal or showed unrelated changes in 42 patients (19 %). Visual assessment correctly lateralised hippocampal sclerosis in 79 of the 84 patients measured (94 %). Temporal lobectomy confirmed the MRI data (side and aetiology) in all 63 operated patients. Patients with normal MRI had an older age of seizure onset and were more often drug-responsive than patients with hippocampal sclerosis. MRI showed temporal lobe abnormalities in 81 % of epileptic patients with varying severity with good neuropathological correlation. Patients with normal MRI had a less severe form of the disease.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    Springer
    Neuroradiology 39 (1997), S. 394-399 
    ISSN: 1432-1920
    Keywords: Key words Pituitary adenoma ; Acromegaly ; Magnetic resonance imaging
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Adenomas causing acromegaly represent at least a quarter of pituitary adenomas. We studied 12 patients presenting with active acromegaly due to a pituitary adenoma with a 1.5 T superconductive MRI unit. All had T1-weighted sagittal and coronal sections before and after Gd-DTPA; six had coronal T2-weighted images. Surgical correlation was obtained in seven patients. Histologically, there were eight growth hormone (GH)-secreting and three mixed [GH and prolactin (PRL) secreting] adenomas, and one secreting GH, PRL and follicle-stimulating hormone. Macroadenomas (10) were more frequent than microadenomas (2). No correlation was found between serum GH and tumour size. There were nine adenomas in the lateral part of the pituitary gland; seven showed lateral or infrasellar invasion. Homogeneous, isointense signal on T1- and T2-weighted images was observed in six cases. Heterogeneous adenomas had cystic or necrotic components.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    Springer
    Neuroradiology 38 (1996), S. 761-768 
    ISSN: 1432-1920
    Keywords: Key words Brain ; magnetic resonance imaging ; Behçet's disease ; Brain ; vasculitis ; Brain ; white matter
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract To study the long-term evolution of cerebral lesions in neuro-Behçet's disease, MRI was carried out on 12 patients, with follow-up from 1.5 to 6 years (mean 3.5 years). On the first MRI, 66 lesions in all were found; each patient had 1–10 lesions (mean 5.5). There were 30 (46 %) lesions in the brain stem, 18 (27 %) in the basal ganglia region and 18 (27 %) in the periventricular white matter. Of these 22 (33 %) were small, 31 (47 %) medium-size and 13 (20 %) large lesions. On the last MRI, 60 lesions were found; each patient had 1–10 lesions (mean 5). At this time 31 lesions (52 %) were in the brain stem, 13 (22 %) in the basal ganglia region and 16 (26 %) in the periventricular white matter. There were 41 (68 %) small, 13 (22 %) medium-size and 6 (10 %) large lesions. About 40 % of the lesions disappeared, 35 % reduced in size and 25 % remained unchanged. No lesion had enlarged. Of the 60 final lesions 20 (34 %) were not observed on the first study. Small new lesions were found in 5 of 12 patients (42 %), and were asymptomatic. Medium-size or large new lesions were found in 2 patients (17 %) who had stopped steroid treatment and had a neurological relapse. Enlargement of the ventricular system or worsening of initial cerebral atrophy was observed in 9 of 12 patients. Appearance of small lesions and worsening of cerebral atrophy on long-term follow-up suggest the possibility of subclinical progression of cerebral vasculitis and should be considered in the prognosis of neuro-Behçet's disease.
    Type of Medium: Electronic Resource
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