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多排螺旋CT平扫结合临床表现在多系统损害结节性硬化症诊断中的应用价值 被引量:7
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作者 张跃 胡颖 张蔚 《中国医疗设备》 2015年第12期57-59,共3页
目的探讨多系统损害结节性硬化症(TSC)的CT影像学特点及临床表现,分析两者结合在TSC诊断中的应用价值。方法回顾性分析经临床或病理确诊的11例TSC患者的CT平扫表现及临床特点。结果 11例患者中仅1例同时具有TSC典型三联征(癫痫、智力低... 目的探讨多系统损害结节性硬化症(TSC)的CT影像学特点及临床表现,分析两者结合在TSC诊断中的应用价值。方法回顾性分析经临床或病理确诊的11例TSC患者的CT平扫表现及临床特点。结果 11例患者中仅1例同时具有TSC典型三联征(癫痫、智力低下及面部皮脂腺瘤),其余10例仅有1种或2种。所有患者均进行了头部或胸腹部CT平扫,11例患者均有室管膜下结节,1例有室管膜下巨细胞星形细胞瘤,4例有肺部非钙化性小结节,8例有肾脏血管平滑肌脂肪瘤,4例有肝脏血管平滑肌脂肪瘤,5例有骨骼受累。结论结合TSC的特征性临床表现及CT平扫征象,可对TSC的确诊提供重要的诊断依据,特别是以癫痫为首发症状且头颅CT平扫有室管膜下结节的患者,更加高度预示了本病的发生。 展开更多
关键词 多排螺旋CT 多系统损害结节性硬化 室管膜下结节 血管平滑肌脂肪瘤
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拉曼光谱技术与神经退行性疾病研究进展 被引量:1
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作者 周珂轩 梁昊岳 孔晓冬 《实用医学杂志》 CAS 北大核心 2021年第22期2950-2954,共5页
随着社会老龄化加重,神经退行性疾病是导致老年人高致病率和残疾率的主要原因,造成重大社会经济负担,受到越来越多的关注。由于其起病隐匿,发展缓慢,病理生理变化复杂,目前尚无明确、特异、可靠的实验室方法对其进行早期诊断。拉曼光谱... 随着社会老龄化加重,神经退行性疾病是导致老年人高致病率和残疾率的主要原因,造成重大社会经济负担,受到越来越多的关注。由于其起病隐匿,发展缓慢,病理生理变化复杂,目前尚无明确、特异、可靠的实验室方法对其进行早期诊断。拉曼光谱技术是一种通过光与物质的相互作用产生的非弹性散射光来进行检测的光学技术,它通过检测分子的散射光来提供细胞、组织或生物流体的化学指纹信息。越来越多的生物医学应用表明,拉曼光谱在检测新的生物标志物方面具有潜力,可以快速准确地筛查疾病的易感性和发病情况,在研究临床相关生物物种、疾病发病机制和诊断方面有广阔的应用前景。本文就拉曼光谱技术对神经退行性疾病的早期诊断方面前景进行概述。 展开更多
关键词 拉曼光谱 阿尔茨海默病 帕金森病 多系统硬化
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Neurogenic bowel dysfunction in patients with spinal cord injury, myelomeningocele, multiple sclerosis and Parkinson’s disease 被引量:21
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作者 Richard A Awad 《World Journal of Gastroenterology》 SCIE CAS CSCD 2011年第46期5035-5048,共14页
Exciting new features have been described concerning neurogenic bowel dysfunction,including interactions between the central nervous system,the enteric nervous system,axonal injury,neuronal loss,neurotransmission of n... Exciting new features have been described concerning neurogenic bowel dysfunction,including interactions between the central nervous system,the enteric nervous system,axonal injury,neuronal loss,neurotransmission of noxious and non-noxious stimuli,and the fields of gastroenterology and neurology.Patients with spinal cord injury,myelomeningocele,multiple sclerosis and Parkinson's disease present with serious upper and lower bowel dysfunctions characterized by constipation,incontinence,gastrointestinal motor dysfunction and altered visceral sensitivity.Spinal cord injury is associated with severe autonomic dysfunction,and bowel dysfunction is a major physical and psychological burden for these patients.An adult myelomeningocele patient commonly has multiple problems reflecting the multisystemic nature of the disease.Multiple sclerosis is a neurodegenerative disorder in which axonal injury,neuronal loss,and atrophy of the central nervous system can lead to permanent neurological damage and clinical disability.Parkinson's disease is a multisystem disorder involving dopaminergic,noradrenergic,serotoninergic and cholinergic systems,characterizedby motor and non-motor symptoms.Parkinson's disease affects several neuronal structures outside the substantia nigra,among which is the enteric nervous system.Recent reports have shown that the lesions in the enteric nervous system occur in very early stages of the disease,even before the involvement of the central nervous system.This has led to the postulation that the enteric nervous system could be critical in the pathophysiology of Parkinson's disease,as it could represent the point of entry for a putative environmental factor to initiate the pathological process.This review covers the data related to the etiology,epidemiology,clinical expression,pathophysiology,genetic aspects,gastrointestinal motor dysfunction,visceral sensitivity,management,prevention and prognosis of neurogenic bowel dysfunction patients with these neurological diseases.Embryological,morphological and experimental studies on animal models and humans are also taken into account. 展开更多
关键词 Neurogenic bowel dysfunction Spinal cordinjury MYELOMENINGOCELE Multiple sclerosis Parkin-son's disease Central nervous system Enteric nervoussystem
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An unusual case of aggressive systemic mastocytosis mimicking hepatic cirrhosis 被引量:2
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作者 Xiao-Yang Zhang Wei-Hua Zhang 《Cancer Biology & Medicine》 SCIE CAS CSCD 2014年第2期134-138,共5页
Hepatic involvement in aggressive systemic mastocytosis(ASM) is relatively common, and the main clinical features of this disease include hepatomegaly, portal hypertension, ascites, and fibrosis. Cirrhosis is a rare A... Hepatic involvement in aggressive systemic mastocytosis(ASM) is relatively common, and the main clinical features of this disease include hepatomegaly, portal hypertension, ascites, and fibrosis. Cirrhosis is a rare ASM symptom. We report an ASM case that initially mimicked cirrhosis based on clinical and radiographic analyses. The portal tract was expanded by mononuclear inflammatory cells, and an increase in collagen amount was observed in routine histological sections of the biopsied liver. A diagnosis of systemic mastocytosis(SM) was made after ancillary tests for mast cells using bone marrow aspirates. Extensive involvement of the liver and gastrointestinal tract was observed. Clinicians and pathologists need to consider ASM as a diagnosis or differential diagnosis in a clinical case of cirrhosis with unknown etiology. The diagnosis can be confirmed or disregarded by immunohistochemical staining and molecular analysis. 展开更多
关键词 Aggressive systemic mastocytosis(ASM) hepatomegaly hepatic fibrosis hepatic cirrhosis
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