amyloidosis

Objective Cardiac amyloidosis ( CAL) is a rare disease and we are not familiar with its clinical features.

目的心肌淀粉样变性（cardiac amyloidosis CAL）是临床上相对少见的疾病，对其临床特点认识不足。

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Localized orbital amyloidosis involving the lacrimal sac and nasolacrimal duct

局部眼眶淀粉样变性病累及泪囊和鼻泪管

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Traumatic purpura occurring in colloid milium may be analogous to that occurring in systemic amyloidosis.

外伤性紫癜胶体粟可能发生类似的发生系统性淀粉样变性。

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Conjunctival Amyloidosis: Report of Six Cases and Review of the Literature

结膜淀粉样变性的6例病例报道和文献综述

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We report a case of pulmonary amyloidosis with multiple pulmonary nodules showing different uptake of18 F-fluorodeoxyglucose ( FDG) on PET.

我们报道报道一例肺多发结节的肺淀粉样变性病例，不同结节在PET上具有不同的摄取FDG表现。

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Cross's disease, familial amyloidosis, prevents the liver from breaking down a protein called transthyretin.

克罗斯患有一种其家族特有的淀粉样变性疾病, 它使肝脏无法分解一种叫做转体基因的蛋白.

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Objective: To investigate the clinical feature, pathogenesis, and therapy of Primary systemic amyloidosis with acquired factor-X deficiency.

目的：探讨原发性系统性淀粉样变性并发凝血因子X缺乏的临床特征、发病机制及治疗方法。

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Objective To investigate the clinicopathologic characteristics of renal amyloidosis.

目的探讨肾脏淀粉样变性的临床病理学特点。

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Objective : To explore the clinical characteristics and pathogenesis of primary systemic amyloidosis.

目的: 探讨原发性系统性淀粉样变病的临床特点和发病机制.

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Perilymphatic distribution is noted in pneumoconiosis, sarcoidosis, amyloidosis.

淋巴管周分布的见于尘肺, 结节病, 淀粉样变性.

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Congo red stain has been performed on the myocardium in a case of amyloidosis.

淀粉样变性心肌经刚果红染色.

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The level of apoptosis in the cardiac amyloidosis is significantly increased.

心脏淀粉样变性中细胞凋亡水平明显增高。

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A case of primary hepatic amyloidosis with factor X deficiency

肝淀粉样变性合并凝血因子X缺乏1例

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Amyloidosis, a disease where abnormal proteins are deposited in tissues, can occur in CD.

淀粉样变性，异常蛋白在组织中积聚的一种疾病，可发生在CD。

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The clinical-pathologic characteristics and misdiagnose causes in 32 patients with renal amyloidosis

肾淀粉样变性病32例临床病理特点及误漏诊分析

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Primary Tracheobronchial Amyloidosis 10 Cases Treated with Bronchoscopy Nd: YAG

经纤支镜激光治疗原发性气管支气管淀粉样变性10例

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Conclusion: The mechanism of factor-X deficiency with primary amyloidosis was known as that the factor-X directly bind to amyloid fibrils and deposit in tissue.

结论：目前认为原发性系统性淀粉样变性并发凝血因子X缺乏的机制是淀粉样纤维与X因子特异性结合沉积在组织中形成的。

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Conclusion Castleman's disease can result in renal amyloidosis, which pathogenic mechanism may be associated with the abnormal immune states caused by Castleman's disease.

结论Castleman病可继发AA型肾淀粉样变性，其发病可能与Castleman病导致的免疫异常有关。

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Primary Hepatic Amyloidosis; A Case Report and Review Literature

原发性肝淀粉样变性1例报告并文献复习

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Pathological examination of the medial rectus muscle showed positive Congo red stain compatible with amyloidosis.

病理切片检查显示阳性刚果红染色反应.

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Objective: To investigate the cardiac function in the patients with amyloidosis by echocardiography, Tissue Doppler Imaging ( DTI) and color M-mode flow propagation velocity ( Vp).

目的：应用超声心动图脉冲多普勒、组织多普勒（DTI）及彩色M型血流传播速率（Vp）技术评价心脏淀粉样变性患者的心脏功能。

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PAS staining of vocal nodules rich in glycogen in epithelial tissues, showing amyloidosis myxoid degeneration.

PAS染色，声带小结组织上皮内糖原丰富，可见淀粉样变性粘液样变性。

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Results AMCH in hemorrhagic cases . The main cause was hypertension, amyloidosis angiopathy and so on.

结果AMCH占同期脑出血的23%, 主要原因为高血压病及淀粉样脑血管病等,其临床表现复杂多样.

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Objective : To improve the diagnostic competence for amyloidosis of larynx both clinically and radiologically.

目的: 提高对喉淀粉样变的临床及影像学诊断水平.

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The Relativity Study between Clinical and TTR Gene Mutation of Familial Vitreous Amyloidosis

家族性玻璃体淀粉样变性的临床及TTR基因突变的相关性研究

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Objective To report a rare case of renal amyloidosis secondary to Castleman's disease, and to review literatures concerned.

目的报道1例罕见的Castleman病继发肾淀粉样变性，并进行相关文献复习。

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Cast nephropathy was the most frequent pathologic type in LWP group, while light chain deposition disease and glomerular amyloidosis were the most common pathologic type in NP group.

肾组织病理上，LWP组以管型肾病最常见，而NP组主要表现为轻链沉积病和肾淀粉样变性。

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Methods: Clinical characteristics, echocardiographic features of cardiac amyloidosis were studied and their chest X-rays, CT scans and serum biochemistry tests were analyzed. Results: ① All patients were more than 55 years.

方法对7例淀粉样变性心肌病患者行超声心动图、X线胸片、电子计算机断层摄影术（CT）及常规血生化检查，分析归纳其临床特点、超声表现及辅助检查结果。

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An uncertain proportion of patients, possibly about 10 per cent, have a third protein abnormality-amyloidosis.

还有一部分(比例不确定)病人可能占10%, 有第三种异常蛋白 —— 淀粉样变性.

词典精选例句

Amyloidosis can go away if the CD disease is successfully treated.

如果CD病被成功的治疗后，淀粉样变性也会消失。

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