Asunto(s)
Infecciones por Virus de Epstein-Barr/complicaciones , Herpesvirus Humano 4/aislamiento & purificación , Trastornos Linfoproliferativos/virología , Tumor de Wilms/complicaciones , Antineoplásicos/uso terapéutico , Preescolar , Dactinomicina/uso terapéutico , Infecciones por Virus de Epstein-Barr/patología , Femenino , Humanos , Trastornos Linfoproliferativos/complicaciones , Trastornos Linfoproliferativos/patología , Rituximab/uso terapéutico , Vincristina/uso terapéutico , Tumor de Wilms/tratamiento farmacológico , Tumor de Wilms/patologíaRESUMEN
Saksenaea species are a rare cause of mucormycosis, the majority associated with cutaneous and subcutaneous infections resulting from trauma in both immunocompromised and immunocompetent individuals. Unlike other causative agents of mucormycosis, cerebral infections are exceptionally rare. We describe the first case of isolated cerebral infection by Saksenaea in a 4-year-old previously healthy male child who presented with headaches. He had no past medical history other than an episode of febrile seizures. In addition to raising the awareness of an unusual presentation of infection by Saksenaea, this case highlights the importance of pathologic examination for the prompt diagnosis of mucormycosis as well as the specific fungal identification for treatment as Saksenaea spp. may be more susceptible to posaconazole and less susceptible to amphotericin B compared to more common causes of mucormycosis.
Asunto(s)
Encefalopatías/patología , Infecciones Protozoarias del Sistema Nervioso Central/patología , Mucormicosis/patología , Encefalopatías/diagnóstico , Neoplasias Encefálicas/diagnóstico , Infecciones Protozoarias del Sistema Nervioso Central/diagnóstico , Preescolar , Diagnóstico Diferencial , Humanos , Masculino , Mucormicosis/diagnósticoRESUMEN
Background and Purpose. To determine whether the pattern of iron deposition in the fascicula nigrale in patients with Parkinson's disease would be different from age-matched controls by utilizing quantitative susceptibility mapping to measure susceptibility change. Methods. MRIs of the brain were obtained from 34 subjects, 18 with Parkinson's disease and 16 age- and gender-matched controls. Regions of interest were drawn around the fascicula nigrale and substantia nigra using SWI mapping software by blinded investigators. Statistical analyses were performed to determine susceptibility patterns of both of these regions. Results. Measurements showed significantly increased susceptibility in the substantia nigra in Parkinson's patients and an increased rostral-caudal deposition of iron in the fascicula nigrale in all subjects. This trend was exaggerated with significant correlation noted with increasing age in the Parkinson group. Conclusion. The pattern of an exaggerated iron deposition gradient of the fascicula nigrale in the Parkinson group could represent underlying tract dysfunction. Significant correlation of increasing iron deposition with increasing age may be a cumulative effect, possibly related to disease duration.
RESUMEN
PURPOSE: To test the ability of susceptibility weighted images (SWI) and high pass filtered phase images to localize and quantify brain iron. MATERIALS AND METHODS: Magnetic resonance (MR) images of human cadaver brain hemispheres were collected using a gradient echo based SWI sequence at 1.5T. For X-ray fluorescence (XRF) mapping, each brain was cut to obtain slices that reasonably matched the MR images and iron was mapped at the iron K-edge at 50 or 100 microm resolution. Iron was quantified using XRF calibration foils. Phase and iron XRF were averaged within anatomic regions of one slice, chosen for its range of iron concentrations and nearly perfect anatomic correspondence. X-ray absorption spectroscopy (XAS) was used to determine if the chemical form of iron was different in regions with poorer correspondence between iron and phase. RESULTS: Iron XRF maps, SWI, and high pass filtered phase data in nine brain slices from five subjects were visually very similar, particularly in high iron regions. The chemical form of iron could not explain poor matches. The correlation between the concentration of iron and phase in the cadaver brain was estimated as c(Fe) [microg/g tissue] = 850Deltavarpi + 110. CONCLUSION: The phase shift Deltavarpi was found to vary linearly with iron concentration with the best correspondence found in regions with high iron content.
Asunto(s)
Encéfalo/patología , Hierro/química , Sincrotrones , Espectroscopía de Absorción de Rayos X/métodos , Enfermedad de Alzheimer/patología , Lesiones Encefálicas/patología , Mapeo Encefálico , Cadáver , Calibración , Formaldehído/farmacología , Humanos , Modelos Estadísticos , Atrofia Muscular/patología , Enfermedad de Parkinson/patologíaRESUMEN
Synchrotron rapid-scanning X-ray fluorescence (RS-XRF) is employed for the first time to simultaneously map iron, copper, and zinc in the normal cerebellum. The cerebellum is a major repository of metals that are essential to normal function. Therefore, mapping the normal metal distribution is an important first step towards understanding how multiple metals may induce oxidative damage, protein aggregation, and neurotoxicity leading to cerebellar degeneration in a wide range of diseases. We found that cerebellar white and grey matter could be sharply defined based upon the unique metal content of each region. The dentate nucleus was particularly metal-rich with copper localized to the periphery and iron and zinc abundant centrally. We discuss how RS-XRF metal mapping in the normal brain may yield important clues to the mechanisms of degeneration in the dentate nucleus.
Asunto(s)
Mapeo Encefálico/métodos , Cerebelo/metabolismo , Cobre/análisis , Hierro/análisis , Espectrometría por Rayos X/métodos , Zinc/análisis , Anciano , Enfermedades Cerebelosas/diagnóstico , Enfermedades Cerebelosas/metabolismo , Enfermedades Cerebelosas/fisiopatología , Núcleos Cerebelosos/química , Núcleos Cerebelosos/citología , Núcleos Cerebelosos/metabolismo , Cerebelo/química , Cerebelo/citología , Cobre/metabolismo , Femenino , Humanos , Hierro/metabolismo , Masculino , Errores Innatos del Metabolismo de los Metales/diagnóstico , Errores Innatos del Metabolismo de los Metales/metabolismo , Errores Innatos del Metabolismo de los Metales/fisiopatología , Fibras Nerviosas Mielínicas/química , Fibras Nerviosas Mielínicas/metabolismo , Fibras Nerviosas Mielínicas/ultraestructura , Neuroquímica/métodos , Neuronas/química , Neuronas/citología , Neuronas/metabolismo , Adulto Joven , Zinc/metabolismoRESUMEN
The clinical diagnosis of many neurodegenerative disorders relies primarily or exclusively on observed behaviors rather than measurable physical tests. One of the hallmarks of Alzheimer disease (AD) is the presence of amyloid-containing plaques associated with deposits of iron, copper and/or zinc. Work in other laboratories has shown that iron-rich plaques can be seen in the mouse brain in vivo with magnetic resonance imaging (MRI) using a high-field strength magnet but this iron cannot be visualized in humans using clinical magnets. To improve the interpretation of MRI, we correlated iron accumulation visualized by X-ray fluorescence spectroscopy, an element-specific technique with T1, T2, and susceptibility weighted MR (SWI) in a mouse model of AD. We show that SWI best shows areas of increased iron accumulation when compared to standard sequences.