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1.
J Endocrinol Invest ; 45(10): 1935-1944, 2022 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-35680695

RESUMEN

OBJECTIVES: Pheochromocytomas are rare tumors which can present with heterogeneous secretion profiles, clinical manifestations, and radiologic appearance. Under a histopathological point of view, they can be characterized as more or less aggressive with the Pheochromocytoma of the Adrenal gland Scaled Score (PASS) and the Grading system for Adrenal Pheochromocytoma and Paraganglioma (GAPP) score. The aim of this study is to analyze the texture analysis characteristics of pheochromocytoma and identify whether the texture analysis can yield information aiding in the diagnosis and the characterization of those tumors. METHODS: Radiological, biochemical, and histopathological data regarding 30 consecutive patients with histologically confirmed pheochromocytoma were analyzed. Images obtained in the unenhanced, late arterial, venous, and delayed phases were used for the texture analysis. RESULTS: Urinary epinephrine and metanephrine levels showed a significant correlation (R2 = 0.946; R2 = 699) in the multivariate linear model with texture features, as well as Ki-67 (R2 = 0.397), PASS score (R2 = 0.182), GAPP score (R2 = 0.705), and cellularity showed a significant correlation (R2 = 0.389). The cluster analysis based on radiomic features resulted in 2 clusters, with significative differences in terms of systolic and diastolic blood pressure values at the time of diagnosis (p = 0.025), GAPP score (4 vs 6, p = 0.05), histological pattern (1-2, p = 0.039), and comedonecrosis (0% vs 50%, p = 0.013). CONCLUSION: In conclusion, our study provides the proof of concept for the use of texture analysis on contrast-enhanced CT images as a noninvasive, quantitative tool for helping in the characterization of the clinical, biochemical, and histopathological features of pheochromocytoma.


Asunto(s)
Neoplasias de las Glándulas Suprarrenales , Paraganglioma , Feocromocitoma , Neoplasias de las Glándulas Suprarrenales/patología , Humanos , Metanefrina , Paraganglioma/patología , Feocromocitoma/diagnóstico por imagen , Feocromocitoma/patología , Estudios Retrospectivos , Tomografía Computarizada por Rayos X/métodos
3.
J Nanosci Nanotechnol ; 8(6): 2912-22, 2008 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-18681027

RESUMEN

Different kinds of magnetic anisotropies have been induced during the nanocrystallization process of Co- and Ni-rich amorphous ferromagnetic (Finemet) ribbons by the application of a constant stress or an axial magnetic field during the annealing process. Magnetization measurements have evidenced the presence od macroscopic anisotropy in the treated samples. The main goal of this work has been, after a careful DSC study, the structural analysis of the treated ribbons using X-ray Diffraction and Atomic Force Microscopy (AFM), detecting substantial differences in the crystallization state and grain size of the samples depending on the thermal treatment that was carried out. Moreover, AFM measurements revealed in all the treated samples a strong nanocrystallisation of the surface without evidences of amorphous matrix, which contrast with XRD measurements that have shown a high content of amorphous phase in the bulk of the ribbons. Magneto-optical Kerr effect measurements have been performed with the aim to elucidate the complex magnetic behaviour that is expected for the surface of the ribbons, measuring surface hysteresis loops that showed much higher coercive field values than that obtained in the bulk material.

4.
Eur J Paediatr Neurol ; 22(5): 822-830, 2018 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-29802023

RESUMEN

BACKGROUND: Neurofibromatosis type 1 is a genetic disorder associated with cognitive deficits, learning disabilities and behavioral problems. These domains appear to have a still controversial debated association with local areas of T2-hyperintensities on MRI images, called unidentified bright objects (UBOs). METHODS: A cohort of 36 children (aged 7-11 years) included consecutively, underwent neuropsychological and behavioral assessment to determine their cognitive and neuropsychological profile, and the frequency of specific learning disabilities. MRI examination was used to determine the impact of UBOs' presence, number, and location on the cognitive, neuropsychological and behavioral profile, and also the presence of optic glioma. RESULTS: The mean full intelligence quotient was 104.6; only one child had mild intellectual disability. Forty one percent of children had a diagnosis of specific learning disabilities and reading was mainly involved. Twenty per cent had attention problems. All children had normal scores in visuo-motor and visuo-perceptual tests. UBOs were present in 94.0% of the MRI examinations. Two children had optic glioma. Children with UBOs in a specific location and children with UBOs elsewhere were statistically compared, no one of the location seemed to have an impact on general cognition measured with full intelligence quotient. The thalamus was associated with problems in calculation and striatum with behavioral problems. An inverse relationship between the number of UBOs and the full intelligence quotient was present, but without a statistical significance. CONCLUSIONS: In this study, the specific location of UBOs did not seem to influence the general cognitive profile and also the relationship between their number and the full intelligence quotient was not significant; these results are still controversial in literature. Finally, the presence of UBOs in the thalamus and striatum may represent a neuroradiological pattern that influences performances in calculation and behavior respectively in children with Neurofibromatosis type 1.


Asunto(s)
Trastornos del Conocimiento/etiología , Trastornos del Conocimiento/patología , Neurofibromatosis 1/patología , Neurofibromatosis 1/psicología , Adolescente , Niño , Trastornos del Conocimiento/epidemiología , Estudios de Cohortes , Femenino , Humanos , Imagen por Resonancia Magnética , Masculino
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