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淀粉样变

网络amyloidosis; DRA; amyloid degeneration

淀粉样变

网络释义

淀粉样变

amyloidosis

淀粉样变(amyloidosis)，亦作类淀粉沉积症，在医学的范畴，是指各种使淀粉样蛋白在身体器官或组织内异常沉积的条件，是 …

DRA

7）透析相关淀粉样变（DRA）是长期血液透析患者最常见的、致残性并发症。在维持性血液透析超过5年的0岁以上患者中，约…

amyloid degeneration

13．神经细胞的淀粉样变(amyloid degeneration)在肌阵挛性癫痫患者的大脑皮质，基底核、脑干及脊髓的神经细胞内有一种同 …

AL amyloidosis

原发型淀粉样变(AL amyloidosis) 发病原因不明，以「多发性骨髓瘤」最常见，造成的原因是因为骨髓中的浆细胞(Plasma cell) …

amyloid change

淀粉样变（amyloid change）：是指细胞外间质内出现淀粉样蛋白的异常沉积。淀粉样物质为结合粘多糖的蛋白质，遇碘时被 …

amyloidosis d

英语... ... electromagnetic d 电磁的由电磁体产生的 amyloidosis d 淀粉样变性病淀粉样变 arteriovenous fistula d 动静脉瘘 ...

ATTR

...个项目所涉及药物，即用于治疗甲状腺素运载蛋白介导的淀粉样变（ATTR）的ALN-TTR01，用于治疗肝癌的ALN-VSP，和 …

例句：

Difficulties with shunts and fistulae for vascular access do not in general seem to be more frequent in patients with amyloid .

建立血透路径的分流和瘘管的困难通常似乎在淀粉样变性病患者中不会增多。

As the name implies, this form of amyloidosis is inherited . This type often affects the liver , nerves, heart and kidneys.

如其名，这种淀粉样变是遗传的，病变通常侵袭肝脏，神经，心脏和肾脏。

Among the heredofamilial forms of amyloidosis , only the Portuguese neuropathic type has so far been studied in any detail .

在家族遗传性的淀粉样变性病中到目前为止只有家族性淀粉样多神经病（葡萄牙型）有详细的研究。

The severity of amyloidosis depends on which organs the amyloid deposits affect.

淀粉样变的严重性依赖于淀粉样蛋白沉积在哪个器官。

Conclusions : Amyloid nephropathy was a kind of infrequent disease, and doctors should heighten cognizance of it.

结论：淀粉样变肾病系少见病，应注意对该病的认识。

This article reviews the research status of pathogenesis and diagnosis as well as the treatment of dialysis related amyloidosis .

有必要对透析相关性淀粉样变的发病机制及诊断与治疗进行探讨。

INTRODUCTION : Amyloidosis is characterized by extracellular deposits of proteins .

导言：淀粉样变性病的特点是外存款的蛋白质。

The place of this drug cannot yet be properly assessed in the management of human amyloidosis .

这个药物的地位在人淀粉样变性病中还不能合适地评价。

And when amyloidosis affects the electrical system of your heart , this may disturb your heart 's rhythm .

当淀粉样变侵袭心脏电传导系统，就会影响到心脏跳动的节律。

The signs and symptoms of amyloidosis are often vague and mimic those of other conditions , so it can be difficult to diagnose amyloidosis.

淀粉样变的症状和体征极难与其他疾病相鉴别，诊断淀粉样变的难度相当大。

Objective To improve the diagnostic rate of local amyloidosis of stomach .

目的提高局限性胃淀粉样变病的诊断率。

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。

and myocardial biopsy, for identifying infiltrative diseases such as myocarditis, amyloidosis, hemochromatosis, and sarcoidosis .

心肌活检对浸润性疾病如心肌炎、淀粉样变、结节病很有用。

Objective : To analyze the causes of misdiagnosis of amyloid nephropathy .

目的：分析淀粉样变肾病病理误诊的原因。

Methods To analyze the clinical and laboratory features in 5 cases of the primary systemic amyloidosis .

方法分析 5 例原发性淀粉样变的临床表现和实验室检查。

Family history . Some cases of amyloidosis are inherited .

家族史、有些病例显示，淀粉样变能遗传。

Still running the new biopsy for amyloidosis ?

还在做淀粉样变性病的活检？。

Has anyone in your family ever been diagnosed with amyloidosis ?

家里有人得过淀粉样变吗？

Method : Reviewed 4 cases of primary amyloidosis of the bladder in our hospital.

方法：回顾性分析 4 例原发性膀胱淀粉样变的临床资料。

The exact cause of primary amyloidosis is unknown , but doctors do know that the disease begins in your bone marrow .

原发性淀粉样变的病因并不明了，但医生可以确定病变起于骨髓。

Age . The majority of people who develop amyloidosis are older than 60 .

淀粉样变患者发病年龄大多高于 60 岁。

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