淀粉样变
- 名amyloidosis
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目的探讨光学显微镜尚未表现明显特点的早期肾淀粉样变(amyloidosis,AL)的临床病理特点及诊断方法。
Objective To investigate the clinicopathological manifestations of early renal amyloidosis ( AL ) and its diagnostic criteria .
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目的了解长期血液透析(HD)患者透析相关性淀粉样变(DRA)的发病率和相关因素。
Objective To investigate the prevalence and risk factors of dialysis-related amyloidosis ( DRA ) .
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结果:PSA在同期淀粉样变中占47.9%。
Results : PSA accounted for 47.9 % of the amyloidosis .
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原发性皮肤淀粉样变患者血清中IL-4及IgE水平测定
Measurement of Serum IgE & IL-4 Level in Primary Amyloidosis of the Skin
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结果A、B两组鸡肝脏都有淀粉样变病发生,血清蛋白质的比例变化和组织学变化有一定关系。
The results show that there was amyloid in livers in both groups A and B , the proposition changes of serum albumin and globulins have some relation with amyloidosis .
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结论:AGE-β2M可能通过与成纤维细胞RAGE的相互作用参与透析相关性淀粉样变的发生。
CONCLUSION : AGE - β 2M may play a role in the pathogenesis of dialysis-related amyloidosis via a pathway involving a fibroblast receptor for AGE .
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方法采用ELISA法测定了46例原发性皮肤淀粉样变患者血清中IL4及IgE水平。
Methods We measured serum IgE & IL-4 of 46 patients with cutaneous amyloidosis by ELISA .
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目的探讨血清IL4及IgE在原发性皮肤淀粉样变中的作用机制。
Objective To investigate the immunological mechanism of cutaneous amyloidosis .
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这一重要过程称之为神经传递,因淀粉样变引起的细胞损伤,而在AD患者脑中则为异常高水平的累积,这被广泛认为是导致AD的原因。
This important process , called neurotransmission , is impaired by amyloid proteins , which build up to abnormally high levels in brains of AD patients and are widely thought to cause the disease .
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方法回顾性对北京协和医院近20a间收治的40例原发性淀粉样变患者的临床表现、诊断及治疗情况进行分析总结。
Methods 40 cases primary amyloidosis diagnosed in our hospital from 1981 to 2001 were retrospectively analyzed .
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目的研究透析相关性淀粉样变(DRA)的声像图特点,评价超声技术对DRA的诊断价值。
Objective To evaluate the value of high resolution ultrasound diagnosing on the dialysis related amyloidosis ( DRA ) .
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结论血清IL4及IgE在原发性皮肤淀粉样变的发生、发展过程中起着重要的作用。
Conclusion It is concluded that serum IL-4 & IgE make important roles in the developing of cutaneous amyloidosis .
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目的探讨长期血液透析患者透析相关淀粉样变(Dialysisrelatedamyloidosis,DRA)的临床及诊治方法。
Objective To discussing the clinical manifestation , diagnosis and treatment of the dialysis-related amyloidosis ( DRA ) in the long-term hemodialysis patients .
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目的:探讨电镜及免疫电镜方法在肾轻链沉积病(lightchaindepositiondisease,LCDD)和轻链型淀粉样变(amyloid,AL)诊断中的作用。
Objective : To investigate the role of electron microscopy ( EM ) and immunoelectron microscopy ( IEM ) in the diagnosis of light chain deposition diseases ( LCDD ) and primary amyloidosis ( AL ) of the kidney .
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结果:52例AMCH占同期脑内出血的8.0%,其中43例(82.7%)有高血压病史,其次为动脉瘤、AVM和脑动脉淀粉样变。
Results : Acute multifocal cerebral hemorrhage was 0.8 % in all cerebral hemorrhage patients during the same period , 43 patients had hypertension history , others had aneurysms , arteriovenous malformation , and cerebral amyloid angiopathy .
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目的进一步提高胸部淀粉样变主的影像认识。
Objective To improve the radiographic knowlege of amyloidosis in thorax .
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淀粉样变肾病误诊为触须样免疫性肾小球病1例分析并文献复习
Misdiagnosis of Amyloid Nephropathy as Immunotactoid glomerulopathy and Its Literature Review
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轻链肾病和轻链型淀粉样变肾脏损害的临床和病理
Clinical and pathological manifestations of light chain nephropathy and primary amyloidosis
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舌活检在原发性系统性淀粉样变性病诊断中的价值
Clinical Value of Lingual Biopsy in Diagnosis of Primary Systemic Amyloidosis
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原发性皮肤淀粉样变淀粉样蛋白组织来源的研究
The Study of Histogenesis of Amyloid in Primary Cutaneous Amyloidosis
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口腔颌面部淀粉样变性病的临床病理研究
Clinicopathological and diagnostic study of amyloidosis of oral maxillofacial area
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继发性者以糖尿病肾病和肾淀粉样变最常见。
Secondary cases the most common type were diabetic and amyloid nephropathy .
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对37例皮肤淀粉样变苔藓进行了临床分析。
The clinical analysis of 37 cases of Lichen amyloidosis was done .
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报告1例舌淀粉样变。
A case of amyloidosis of the tongue is reported .
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目的提高局限性胃淀粉样变病的诊断率。
Objective To improve the diagnostic rate of local amyloidosis of stomach .
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报告1例原发性系统性淀粉样变病。
A case of primary systemic amyloidosis ( PSA ) is reported .
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用甲紫快速染色诊断皮肤淀粉样变
Diagnosis of Cutaneous Amyloidosis by Rapid Stain with Methyl Violet
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家族性遗传性淀粉样变性病2例,均以神经系统受累症状为主。
Two cases of familial amyloidosis were both neuropathic type .
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原发性系统性淀粉样变的消化系统临床表现和诊断
Clinical Characteristics and Diagnosis of Gastrointestinal Primary Systemic Amyloidosis
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系统性淀粉样变的呼吸系统表现
The clinic features of respiratory tract in systemic amyloidosis