28 resultados para nuclear resonance, medical diagnostic, lung
Resumo:
Polychlorinated trityl radicals bearing carboxylate substituents are water soluble persistent radicals that can be used for dynamic nuclear polarization. In contrast to other trityl radicals, the polarization mechanism differs from the classical solid effect. DFT calculations performed to rationalize this behaviour support the hypothesis that polarization is transferred from the unpaired electron to chlorine nuclei and from these to carbon by spin diffusion. The marked differences observed between neutral and anionic forms of the radical will be discussed.
Resumo:
We present a 53-year-old man with a vocal cord paralysis observed as a primary manifestation of lung carcinoma. Tc-99m MDP whole body bone scan were performed and resulted a normal scintiscan. The bone scan does not revealed suspicious foci of uptake. The possibility of bone metastasis was taken into consideration. A whole body F18-FDG-PET scan showed intense uptake in the left upper lung corresponding to the primary tumor. A bronchial biopsy confirmed infiltration by small cell lung carcinoma (SCLC). SCLC is composed of poorly differentiated, rapidly growing cells with disease usually occurring centrally rather than peripherally. It metastasizes early. The whole-body F18-FDG-PET scan clearly demonstrated a focus of increased uptake in the second lumbar vertebral body suspicious for osteolytic metastasis. A lytic bone metastasis was confirmed by MRI. The patient then received therapy and underwent follow up abdominal CT. The scan showed blastic changes in the L2 vertebra suggesting response to treatment.
Resumo:
Members of the histone-like nucleoid structuring protein (H-NS) family play roles both as architectural proteins and as modulators of gene expression in Gram-negative bacteria. The H-NS protein participates in modulatory processes that respond to environmental changes in osmolarity, pH, or temperature. H-NS oligomerization is essential for its activity. Structural models of different truncated forms are available. However, high-resolution structural details of full-length H-NS and its DNA-bound state have largely remained elusive. We report on progress in characterizing the biologically active H-NS oligomers with solid-state NMR. We compared uniformly ((13)C,(15)N)-labeled ssNMR preparations of the isolated N-terminal region (H-NS 1-47) and full-length H-NS (H-NS 1-137). In both cases, we obtained ssNMR spectra of good quality and characteristic of well-folded proteins. Analysis of the results of 2D and 3D (13)C-(13)C and (15)N-(13)C correlation experiments conducted at high magnetic field led to assignments of residues located in different topological regions of the free full-length H-NS. These findings confirm that the structure of the N-terminal dimerization domain is conserved in the oligomeric full-length protein. Small changes in the dimerization interface suggested by localized chemical shift variations between solution and solid-state spectra may be relevant for DNA recoginition.
Resumo:
We compute the shift in the frequency of the spin resonance in a solid that rotates in the field of a circularly polarized electromagnetic wave. Electron-spin resonance, nuclear magnetic resonance, and ferromagnetic resonance are considered. We show that contrary to the case of the rotating LC circuit, the shift in the frequency of the spin resonance has strong dependence on the symmetry of the receiver. The shift due to rotation occurs only when rotational symmetry is broken by the anisotropy of the gyromagnetic tensor, by the shape of the body or by magnetocrystalline anisotropy. General expressions for the resonance frequency and power absorption are derived and implications for experiment are discussed.
Resumo:
La presente entrega de la serie de Nursing sobre pruebas complementarias está dedicada a la gammagrafía. La gammagrafía es una técnica de diagnóstico por la imagen de medicina nuclear. Las exploraciones de medicina nuclear se pueden clasificar en medicina nuclear convencional (gammagrafía) y medicina nuclear por tomografía por emisión de positrones (PET), que se estudiará en la siguiente entrega de Nursing sobre pruebas complementarias. La gammagrafía es una técnica diagnóstica que utiliza sustancias radiactivas (isótopos) para estudiar la anatomía y el funcionalismo de diferentes órganos y tejidos del cuerpo. La gran ventaja de esta modalidad diagnóstica es su carácter funcional y su capacidad para evidenciar procesos pre-anatómicos de desarrollo patológico o anómalo que, junto con su elevada sensibilidad, permite diagnosticar alteraciones en fases muy precoces para poder ser tratadas. En el presente artículo se exponen las pruebas diagnósticas de gammagrafía más habituales, teniendo en cuenta que también existe la posibilidad de tratamientos terapéuticos que no son objeto de este trabajo. La enfermera, además del cuidado del paciente durante la preparación y después de la técnica, puede resolver las inquietudes relacionadas con las exploraciones gammagráficas, que normalmente tienen que ver con las características de cada prueba, la duración y el grado de molestia.
Resumo:
La presente entrega de la serie de Nursing sobre las pruebas complementarias está dedicada a la tomografía por emisión de positrones o PET, acrónimo de positron emission tomography. La PET es una técnica de diagnóstico por la imagen de medicina nuclear en la cual se administra al paciente un radiofármaco emisor de positrones. Este radiofármaco se incorpora a los tejidos adecuados siguiendo una vía metabólica determinada. La radiactividad emitida por esos tejidos del paciente es detectable por los equipos PET y se obtienen imágenes que proporcionan una información funcional in vivo. El radiofármaco PET más habitual es un análogo de la glucosa que se llama F-18-fluordesoxiglucosa, conocido como FDG, el cual permite estudiar la actividad metabólica. La incorporación de la tomografía computarizada (TC) en el mismo equipo híbrido PET-TC permite obtener además la información anatómica del paciente. En el presente artículo se describen los fundamentos físicos y fisiológicos básicos de las exploraciones PET-TC con FDG en oncología, así como los procedimientos de enfermería necesarios para el cuidado del paciente y la correcta obtención de las imágenes.
Resumo:
La presente entrega de la serie de Nursing sobre pruebas complementarias está dedicada a la gammagrafía. La gammagrafía es una técnica de diagnóstico por la imagen de medicina nuclear. Las exploraciones de medicina nuclear se pueden clasificar en medicina nuclear convencional (gammagrafía) y medicina nuclear por tomografía por emisión de positrones (PET), que se estudiará en la siguiente entrega de Nursing sobre pruebas complementarias. La gammagrafía es una técnica diagnóstica que utiliza sustancias radiactivas (isótopos) para estudiar la anatomía y el funcionalismo de diferentes órganos y tejidos del cuerpo. La gran ventaja de esta modalidad diagnóstica es su carácter funcional y su capacidad para evidenciar procesos pre-anatómicos de desarrollo patológico o anómalo que, junto con su elevada sensibilidad, permite diagnosticar alteraciones en fases muy precoces para poder ser tratadas. En el presente artículo se exponen las pruebas diagnósticas de gammagrafía más habituales, teniendo en cuenta que también existe la posibilidad de tratamientos terapéuticos que no son objeto de este trabajo. La enfermera, además del cuidado del paciente durante la preparación y después de la técnica, puede resolver las inquietudes relacionadas con las exploraciones gammagráficas, que normalmente tienen que ver con las características de cada prueba, la duración y el grado de molestia.
Resumo:
La presente entrega de la serie de Nursing sobre las pruebas complementarias está dedicada a la tomografía por emisión de positrones o PET, acrónimo de positron emission tomography. La PET es una técnica de diagnóstico por la imagen de medicina nuclear en la cual se administra al paciente un radiofármaco emisor de positrones. Este radiofármaco se incorpora a los tejidos adecuados siguiendo una vía metabólica determinada. La radiactividad emitida por esos tejidos del paciente es detectable por los equipos PET y se obtienen imágenes que proporcionan una información funcional in vivo. El radiofármaco PET más habitual es un análogo de la glucosa que se llama F-18-fluordesoxiglucosa, conocido como FDG, el cual permite estudiar la actividad metabólica. La incorporación de la tomografía computarizada (TC) en el mismo equipo híbrido PET-TC permite obtener además la información anatómica del paciente. En el presente artículo se describen los fundamentos físicos y fisiológicos básicos de las exploraciones PET-TC con FDG en oncología, así como los procedimientos de enfermería necesarios para el cuidado del paciente y la correcta obtención de las imágenes.
Resumo:
Peer-reviewed
Resumo:
The design and synthesis of Lamellarin D conjugates with a nuclear localization signal peptide and a poly(ethylene glycol)-based dendrimer are described. Conjugates 1-4 were obtained in 8-84% overall yields from the corresponding protected Lamellarin D. Conjugates 1 and 4 are 1.4 to 3.3-fold more cytotoxic than the parent compound against three human tumor cell lines(MDA-MB-231 breast, A-549 lung, and HT-29 colon). Besides, conjugates 3, 4 showed a decrease in activity potency in BJ skin fibroblasts, a normal cell culture. Cellular internalization was analyzed and nuclear distribution pattern was observed for 4, which contains a nuclear localization signalling sequence.
Resumo:
Ewing sarcoma or primitive neuroectodermal tumor (PNET) of bone is the second most common pediatric malignant bone tumor. The median age at diagnosis is 15 years and there is a male predilection of 1.5/1. The authors present the case of a 14-year-old boy with Ewing sarcoma situated on the left ninth rib which was being investigated for respiratory tract infection. Pleurisy is the most common misdiagnosis. Our case illustrates the importance of recognizing exceptional features when interpreting FDG PET or scintigraphy to prevent the misinterpretation of metastases as other etiologies, such as infection.
Resumo:
We present a 53-year-old man with a vocal cord paralysis observed as a primary manifestation of lung carcinoma. Tc-99m MDP whole body bone scan was performed and resulted in a normal scintiscan. The bone scan did not reveal any suspicious foci of uptake. The possibility of bone metastasis was taken into consideration. A whole body F18-FDG-PET scan showed intense uptake in the left upper lung corresponding to the primary tumor. A bronchial biopsy confirmed infiltration by small cell lung carcinoma (SCLC). SCLC is composed of poorly differentiated, rapidly growing cells with diseases usually occurring centrally rather than peripherally. It metastasizes early. The whole-body F18-FDG-PET scan clearly demonstrated a focus of increased uptake in the second lumbar vertebral body suspicious for osteolytic metastasis. A lytic bone metastasis was confirmed by MRI. The patient then received therapy and underwent follow up abdominal CT. The scan showed blastic changes in the L2 vertebra suggesting response to treatment.
Resumo:
Background: Assessing of the costs of treating disease is necessary to demonstrate cost-effectiveness and to estimate the budget impact of new interventions and therapeutic innovations. However, there are few comprehensive studies on resource use and costs associated with lung cancer patients in clinical practice in Spain or internationally. The aim of this paper was to assess the hospital cost associated with lung cancer diagnosis and treatment by histology, type of cost and stage at diagnosis in the Spanish National Health Service. Methods: A retrospective, descriptive analysis on resource use and a direct medical cost analysis were performed. Resource utilisation data were collected by means of patient files from nine teaching hospitals. From a hospital budget impact perspective, the aggregate and mean costs per patient were calculated over the first three years following diagnosis or up to death. Both aggregate and mean costs per patient were analysed by histology, stage at diagnosis and cost type. Results: A total of 232 cases of lung cancer were analysed, of which 74.1% corresponded to non-small cell lung cancer (NSCLC) and 11.2% to small cell lung cancer (SCLC); 14.7% had no cytohistologic confirmation. The mean cost per patient in NSCLC ranged from 13,218 Euros in Stage III to 16,120 Euros in Stage II. The main cost components were chemotherapy (29.5%) and surgery (22.8%). Advanced disease stages were associated with a decrease in the relative weight of surgical and inpatient care costs but an increase in chemotherapy costs. In SCLC patients, the mean cost per patient was 15,418 Euros for limited disease and 12,482 Euros for extensive disease. The main cost components were chemotherapy (36.1%) and other inpatient costs (28.7%). In both groups, the Kruskall-Wallis test did not show statistically significant differences in mean cost per patient between stages. Conclusions: This study provides the costs of lung cancer treatment based on patient file reviews, with chemotherapy and surgery accounting for the major components of costs. This cost analysis is a baseline study that will provide a useful source of information for future studies on cost-effectiveness and on the budget impact of different therapeutic innovations in Spain.