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61.
眩晕患者的诊断过程始于对病史以及随后的全身体格检查和神经系统检查的准确评价。这步骤通常能够识别确切的病因,或者至少可鉴别周围性眩晕和中枢性眩晕。神经放射学检查必须作为选择性诊断手段加以考虑,包括CT、MRI、MR血管造影(MRA)以及血管造影术。对于周围性眩晕、良性阵发性位置性眩晕、迷路炎、Meniere病、外淋巴瘘、局部外伤、中毒性迷路炎、急性中耳炎和慢性中耳渗液等疾病的诊断而言,影像学技术的作用是有争议的。CT和MR可用来排除其他病理学原因和证实诊断。分辨率和增加和能够增强迷路内液的特殊MRI序列的应用,使我们能够对迷路的结构和病理学变化进行更详细地分析。T1和T2对比序列检查都是必需的。当怀疑中耳类以及在外伤后眩晕随访时,需要进行高分辨率CT检查。中枢性眩晕的病因很多,包括椎基底循环血管病变、多发性硬化、偏头痛相关性眩晕、小脑和脑干肿瘤以及中枢神经系统感染,其中脑缺血和多发性硬化最为常见。在这些情况下,影像学检查应该是强制性的。CT能够诊断大多数小脑出血以及小脑和脑干的急性缺血,增强的MRI已经证实是检测后颅窝病病变最为敏感的工具。弥散加权MRI能够比常规MRI更早地显示急性缺血性改变。MRA能提供类似血管造影片的颅内血管图像。有证据表明,有时可避免进行侵入性的血管造影术。MRA的分辨率不如传统的血管造影术,还可能受到活动和其他伪影的影响。选择性的后循环血管造影通常对治疗决策有提示作用。 相似文献
62.
Morphological variation of layer III pyramidal neurones in the occipitotemporal pathway of the macaque monkey visual cortex 总被引:5,自引:5,他引:0
We compared the morphological characteristics of layer III pyramidal
neurones in different visual areas of the occipitotemporal cortical
'stream', which processes information related to object recognition in the
visual field (including shape, colour and texture). Pyramidal cells were
intracellularly injected with Lucifer Yellow in cortical slices cut
tangential to the cortical layers, allowing quantitative comparisons of
dendritic field morphology, spine density and cell body size between the
blobs and interblobs of the primary visual area (V1), the interstripe
compartments of the second visual area (V2), the fourth visual area (V4)
and cytoarchitectonic area TEO. We found that the tangential dimension of
basal dendritic fields of layer III pyramidal neurones increases from
caudal to rostral visual areas in the occipitotemporal pathway, such that
TEO cells have, on average, dendritic fields spanning an area 5-6 times
larger than V1 cells. In addition, the data indicate that V1 cells located
within blobs have significantly larger dendritic fields than those of
interblob cells. Sholl analysis of dendritic fields demonstrated that
pyramidal cells in V4 and TEO are more complex (i.e. exhibit a larger
number of branches at comparable distances from the cell body) than cells
in V1 or V2. Moreover, this analysis demonstrated that the dendrites of
many cells in V1 cluster along specific axes, while this tendency is less
marked in extrastriate areas. Most notably, there is a relatively large
proportion of neurones with 'morphologically orientation-biased' dendritic
fields (i.e. branches tend to cluster along two diametrically opposed
directions from the cell body) in the interblobs in V1, as compared with
the blobs in V1 and extrastriate areas. Finally, counts of dendritic spines
along the length of basal dendrites revealed similar peak spine densities
in the blobs and the interblobs of V1 and in the V2 interstripes, but
markedly higher spine densities in V4 and TEO. Estimates of the number of
dendritic spines on the basal dendritic fields of layer III pyramidal cells
indicate that cells in V2 have on average twice as many spines as V1 cells,
that V4 cells have 3.8 times as many spines as V1 cells, and that TEO cells
have 7.5 times as many spines as V1 cells. These findings suggest the
possibility that the complex response properties of neurones in rostral
stations in the occipitotemporal pathway may, in part, be attributed to
their larger and more complex basal dendritic fields, and to the increase
in both number and density of spines on their basal dendrites.
相似文献
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A 22 year old male presented with symptoms of diffuse muscle pain and multiple abnormal laboratory findings that were eventually attributed to tropical myositis. Computed tomography scan was more reliable than ultrasound and served as a guide to needle aspiration and pathologic diagnosis. 相似文献
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Alpha-thalassemia in two Mediterranean populations 总被引:5,自引:0,他引:5
Pirastu M; Lee KY; Dozy AM; Kan YW; Stamatoyannopoulos G; Hadjiminas MG; Zachariades Z; Angius A; Furbetta M; Rosatelli C; Cao A 《Blood》1982,60(2):509-512
We used restriction endonuclease analysis to determine the incidence of alpha-thalassemia in two Mediterranean islands. In a random population sample, the gene frequency of deletion-type alpha-thalassemia-2 (- alpha) was 0.18 in Sardinians and 0.07 in Greek Cypriots. All cases were the rightward crossover type. From these frequencies and the known incidence of hemoglobin-H disease in these populations, we calculated the frequency of the alpha-thalassemia-1 genotype (--) and determined that it was low. We also found that beta-thalassemia homozygotes in sardinia have a higher incidence of alpha-thalassemia than normals and beta thalassemia heterozygotes because a significantly greater number of these homozygotes are also homozygous for the alpha-thalassemia-2 lesion. These findings support the theory that coinheritance of alpha- thalassemia mitigates the severity of beta-thalassemia and suggest that the protection is most pronounced when two alpha-globin genes are deleted. 相似文献