18 research outputs found

    [Anatomoclinical study of a case with metamorphopsia restricted to faces and familiar objects]

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    The case of a 19-year old patient suffering of transient metamorphopsia restricted to familiar faces and familiar objects is reported. This clinical sign resulted from a small right occipitotemporal haemorrhage due to a sub-cortical metastasis. The patient claimed that faces are distorded and look more pleasant. There were neither visual field defects nor visual agnosia. MRI revealed a small high signal area in the right fusiform gyrus. The structural and functional aspects of the metamorphopsia are documented and discussed in relation to aperceptive prosopagnosia. More specifically, it is suggested that facial metamorphopsia and aperceptive prosopagnosia express the same underlying disorder differing only in terms of severity

    Etude d'un cas de métamorphopsie limitée aux visages et à certains objets familiers.

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    The case of a 19-year old patient suffering of transient metamorphopsia restricted to familiar faces and familiar objects is reported. This clinical sign resulted from a small right occipitotemporal haemorrhage due to a sub-cortical metastasis. The patient claimed that faces are distorted and look more pleasant. There were neither visual field defects nor visual agnosia. MRI revealed a small high signal area in the right fusiform gyrus. The structural and functional aspects of the metamorphopsia are documented and discussed in relation to aperceptive prosopagnosia. More specifically, it is suggested that facial metamorphopsia and aperceptive prosopagnosia express the same underlying disorder differing only in terms of severity

    Nature of the inhibition layer in GA baths

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    International audienceThe nature of the intermetallic layer which forms on the steel surface during immersion in typical galvanizing baths for galvannealed (GA) sheets production has been investigated on two commercial Titanium-stabilized Interstitial-Free (Ti-IF) steel substrates galvanized in baths with different Al contents. Results from this study show that in both cases the inhibition layer is biphasic and composed of a very thin Al-rich phase layer, identified as Fe2Al5Znx, and a thicker Zn-rich phase layer on top of it, identified as Ύ. Experimental results also show that the Fe2Al5Znx phase layer becomes discontinuous when decreasing the bath Al content. Discussions about the mechanisms of formation and the final microstructure of this inhibiting layer are also tackled in this paper by means of the Al-Fe-Zn ternary phase diagram at 460 °C and assumptions to justify any deviation from thermodynamic equilibrium are as well proposed

    Whole brain quantitative CBF and CBV measurements using MRI bolus tracking: comparison of methodologies.

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    Three different deconvolution techniques for quantifying cerebral blood flow (CBF) from whole brain T*(2)-weighted bolus tracking images were implemented (parametric Fourier transform P-FT, parametric single value decomposition P-SVD and nonparametric single value decomposition NP-SVD). The techniques were tested on 206 regions from 38 hyperacute stroke patients. In the P-FT and P-SVD techniques, the tissue and arterial concentration time curves were fit to a gamma variate function and the resulting CBF values correlated very well (CBF(P-FT) = 1.02 x CBF(P-SVD), r(2) = 0.96). The NP-SVD CBF values (i.e., original unfitted curves were used) correlated well with the P-FT CBF values only when a sufficient number of time series volumes were acquired to minimize tracer time curve truncation (CBF(P-FT) x 0.92 x CBF(NP-SVD), r(2) = 0.88). The correlation between the fitted CBV and the unfitted CBV values was also maximized in regions with minimal tracer time curve truncation (CBV(fit) = 1.00 x CBV(unfit), r(2) = 0.89). When a sufficient number of time series volumes could not be acquired (due to scanner limitations) to avoid tracer time curve truncation, the P-FT and P-SVD techniques gave more reliable estimates of CBF than the NP-SVD technique

    [Diffusion- and perfusion-weighted MR imaging during the hyperacute phase of stroke.]

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    The sensitivity of diffusion-weighted MR imaging to detect a lesion within 6 hours of stroke onset was approximately 90%. The false negative results were usually small lesions (less than or equal to 1 ml), were seen early, and were usually located in the brain stem. The specificity of this technique was nearly 100% when it was used correctly. The volume and the value of the apparent diffusion coefficient of the detected lesions provided prognostic information. After injection of a contrast agent (perfusion imaging), a time series of volumes were obtained using a T2* sensitive gradient echo EPI sequence. Hemodynamic perturbations of the cerebral parenchyma could be detected as well as the type of perturbation in the lesion. A map representing the mean transit time for each voxel was used to define the maximum volume of the perturbation. A hemodynamic penumbra was defined to be when this volume was larger than the volume detected on the diffusion images. The quantitative measure of cerebral blood flow could predict the irreversibility of the lesions when the value was below 18ml/min/100g, and the extension of the ischemia in the penumbra zone when the value was below a threshold of 30ml/min/100g

    Whole brain quantitative CBF, CBV, and MTT measurements using MRI bolus tracking: implementation and application to data acquired from hyperacute stroke patients.

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    A robust whole brain magnetic resonance (MR) bolus tracking technique based on indicator dilution theory, which could quantitatively calculate cerebral blood flow (CBF), cerebral blood volume (CBV), and mean transit time (MTT) on a regional basis, was developed and tested. T2*-weighted gradient-echo echoplanar imaging (EPI) volumes were acquired on 40 hyperacute stroke patients after gadolinium diethylene triamine pentaacetic acid (Gd-DTPA) bolus injection. The thalamus, white matter (WM), infarcted area, penumbra, and mirror infarcted and penumbra regions were analyzed. The calculation of the arterial input function (AIF) needed for absolute quantification of CBF, CBV, and MTT was shown to be user independent. The CBF values (ml/min/100 g units) and CBV values (% units, in parentheses) for the thalamus, WM, infarct, mirror infarct, penumbra, and mirror penumbra (averaged over all patients) were 69.8 +/- 22.2 (9.0 +/- 3.0 SD); 28.1 +/- 6.9 (3.9 +/- 1.2); 34.4 +/- 22.4 (7.1 +/- 2.7); 60.3 +/- 20.7 (8.2 +/- 2.3); 50.2 +/- 17.5 (10.4 +/- 2.4); and 64.2 +/- 17.0 (9.5 +/- 2.3), respectively, and the corresponding MTT values (in seconds) were 8.0 +/- 2.1; 8.6 +/- 3.0; 16.1 +/- 8.9; 8.6 +/- 2.9; 13.3 +/- 3.5; and 9.4 +/- 3.2. The infarct and penumbra CBV values were not significantly different from their corresponding mirror values, whereas the CBF and MTT values were (P < 0.01). Quantitative measurements of CBF, CBV, and MTT were calculated on a regional basis on data acquired from hyperacute stroke patients, and the CBF and MTT values showed greater sensitivity to areas with perfusion defects than the CBV values. J. Magn. Reson. Imaging 2000;12:400-410

    Imageries de diffusion et de perfusion en IRM à la phase hyperaiguë d'un accident vasculaire cérébral ischémique.

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    The sensitivity of diffusion-weighted MR imaging to detect a lesion within 6 hours of stroke onset was approximately 90%. The false negative results were usually small lesions (1 ml), were seen early, and were usually located in the brain stem. The specificity of this technique was nearly 100% when it was used correctly. The volume and the value of the apparent diffusion coefficient of the detected lesions provided prognostic information. After injection of a contrast agent (perfusion imaging), a time series of volumes were obtained using a T2* sensitive gradient echo EPI sequence. Hemodynamic perturbations of the cerebral parenchyma could be detected as well as the type of perturbation in the lesion. A map representing the mean transit time for each voxel was used to define the maximum volume of the perturbation. A hemodynamic penumbra was defined to be when this volume was larger than the volume detected on the diffusion images. The quantitative measure of cerebral blood flow could predict the irreversibility of the lesions when the value was below 18 ml/min/100g, and the extension of the ischemia in the penumbra zone when the value was below a threshold of 30 ml/min/100g

    Usefulness of magnetic resonance-derived quantitative measurements of cerebral blood flow and volume in prediction of infarct growth in hyperacute stroke.

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    BACKGROUND AND PURPOSE: The identification of the tissue at risk for infarction remains challenging in stroke patients. In this study, we evaluated the value of quantitative cerebral blood flow (CBF) and cerebral blood volume (CBV) measurements in the prediction of infarct growth in hyperacute stroke. METHODS: Fluid-attenuated inversion recovery (FLAIR), diffusion-weighted (DW), and gradient-echo echo-planar perfusion-weighted (PW) sequences were obtained in 66 patients within 6 hours of stroke onset; ischemia was confirmed on follow-up FLAIR images. We delineated the following: (1) the initial infarct on DW images, (2) the area of hemodynamic disturbance on mean transit time (MTT) maps, and (3) the final infarct on follow-up FLAIR images. MTT, CBF, and CBV were calculated in the following areas: area of initial infarct (INF), area of infarct growth (IGR, final minus initial infarct), the hemodynamically disturbed area that remained viable (OLI, hemodynamic disturbance minus final infarct), and all contralateral mirror regions. RESULTS: Compared with mirror regions, the MTT in abnormal areas was always prolonged. The respective mean+/-SD CBF and CBV values were as follows: for INF, 28+/-16 mL/min per 100 g and 6.9+/-2.7%; for IGR, 36+/-20 mL/min per 100 g and 8.9+/-3.1%; for OLI, 50+/-17 mL/min per 100 g and 11.2+/-3%; and for mirror regions, 64+/-23 mL/min per 100 g and 8.7+/-2.5%. The CBV and CBF values were significantly different between all abnormal areas (except for the CBF between INF and IGR). In the area of DW/PW mismatch, a combined CBF or CBV threshold of 35 or 8.2, respectively, predicted evolution to infarction with a sensitivity of 81% and a specificity of 76%. CONCLUSIONS: Quantitative measurements of CBF and CBV in hyperacute stroke may help to predict infarct growth and to select the subjects who will benefit from thrombolysis
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