Suppr超能文献

[原发性局限性膀胱淀粉样变性]

[Primary localized bladder amyloidosis].

作者信息

Haouas N, Colas J M

机构信息

Service d'urologie, Centre hospitalier Louis Pasteur, Avenue Léon Jouhaux, 39100 Dole Cedex.

出版信息

Rev Med Suisse. 2007 May 23;3(112):1334-6.

Abstract

Amyloidosis constitutes a group of storage diseases concerning various proteins, classified as a function of the type of protein. Localized pseudo tumoral amyloidosis of the urinary tract is a rare affection with bladder like the most frequent localisation. In spite of contribution of computerized tomography scans and MRI, the diagnosis is always based on histological examination of cystoscopy samples. Investigations are required to eliminate a generalized amyloidosis or a malignant lymphoproliferation. Treatment should be as conservative as possible on the outside of a massive and recurrent haematuria to be able to involve vital prognosis.

摘要

淀粉样变性是一组涉及多种蛋白质的贮积病,根据蛋白质类型进行分类。泌尿道局限性假肿瘤性淀粉样变性是一种罕见疾病,膀胱是最常见的发病部位。尽管计算机断层扫描和磁共振成像有所帮助,但诊断仍始终基于膀胱镜检查样本的组织学检查。需要进行相关检查以排除全身性淀粉样变性或恶性淋巴增殖性疾病。除了大量反复血尿可能影响重要预后外,治疗应尽可能保守。

相似文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验