• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

意义未明的单克隆丙种球蛋白病。397例的临床病程及生物学特征

[Monoclonal gammopathies of undetermined significance. Clinical course and biological aspects of 397 cases].

作者信息

Giraldo M P, Rubio-Félix D, Perella M, Gracía J A, Bergua J M, Giralt M

机构信息

Servicio Regional de Hematología y Hemoterapia, Hospital Miguel Servet.

出版信息

Sangre (Barc). 1991 Oct;36(5):377-82.

PMID:1816635
Abstract

The diagnostic criteria, incidence, clinical characteristics and outcome of 397 patients with monoclonal gammopathies of undetermined significance, all of them diagnosed and followed-up at the Haematology Service of the Miguel Servet Hospital, in Zaragoza, between January 1970 and December 1988, were revised. The patients' mean age was 64.7 years (range: 2-89). The M/F ratio was 236/161. The mean concentration of the M component (MC) was 1.17 g/dL (range: 0.20-3.50), this being under 0.50 in 65 cases. IgG was the most frequent MC (71.26%), followed by IgA (14.34%) and IgM (10.82%). Multiple MC was present in 14 cases (3.58). Light chains were passed in urine by 33 patients (8.31%). No associated pathology was found in 213 patients (53.65%) upon MC discovery, while 65 other (16.31%) were carriers of different blood disorders, chronic lymphoproliferative diseases being the commonest (11.57%). In 30 patients (7.30%) the MC was associated to nonhaematological malignancies, and 29 others had an underlying chronic infection. Chronic liver disease was present in 25 cases, and autoimmune disease in 14. Transient monoclonal gammopathy was seen in a small group of patients (6.54%), most of them suffering from acute infectious illness. With regard to the group of patients without any associated pathology, their median follow-up was 37.8 months (range: 18-228). Of them, the MC kept unchanged in 134 cases (62.91%); 47(22.06%) died from any unrelated cause, and 10 others evolved into malignant monoclonal gammopathy. The median clinical course of these last expanded to 60 months (range: 11-124), with an accumulated actuarial risk of 4.5% at 5 years, 15% at 10 years and 26% at 15 years.

摘要

对1970年1月至1988年12月期间在萨拉戈萨米格尔·塞尔维特医院血液科确诊并随访的397例意义未明的单克隆丙种球蛋白病患者的诊断标准、发病率、临床特征及转归进行了回顾。患者的平均年龄为64.7岁(范围:2至89岁)。男女比例为236/161。M成分(MC)的平均浓度为1.17 g/dL(范围:0.20至3.50),65例患者的MC浓度低于0.50。IgG是最常见的MC(71.26%),其次是IgA(14.34%)和IgM(10.82%)。14例患者(3.58%)存在多种MC。33例患者(8.31%)尿中出现轻链。发现MC时,213例患者(53.65%)未发现相关病变,另外65例(16.31%)患有不同的血液疾病,最常见的是慢性淋巴细胞增殖性疾病(11.57%)。30例患者(7.30%)的MC与非血液系统恶性肿瘤相关联,另外29例有潜在的慢性感染。25例患者存在慢性肝病,14例有自身免疫性疾病。一小部分患者(6.54%)出现短暂性单克隆丙种球蛋白病,其中大多数患有急性感染性疾病。对于无任何相关病变的患者组,他们的中位随访时间为37.8个月(范围:18至228个月)。其中,134例患者(62.91%)的MC保持不变;47例(22.06%)死于任何无关原因,另外10例进展为恶性单克隆丙种球蛋白病。最后这组患者的中位病程延长至60个月(范围:11至124个月),5年累积精算风险为4.5%,10年为15%(此处原英文有误,根据语境推测为15%),15年为26%。

相似文献

1
[Monoclonal gammopathies of undetermined significance. Clinical course and biological aspects of 397 cases].意义未明的单克隆丙种球蛋白病。397例的临床病程及生物学特征
Sangre (Barc). 1991 Oct;36(5):377-82.
2
[Incidence, clinico-biological characteristics, and clinical course of 1,203 monoclonal gammopathies (1971-1992)].
Sangre (Barc). 1994 Oct;39(5):343-50.
3
[Multiple myeloma after monoclonal gammopathy of uncertain significance. Study of 10 patients].意义未明的单克隆丙种球蛋白病后发生的多发性骨髓瘤。10例患者的研究
Sangre (Barc). 1993 Oct;38(5):371-4.
4
[Monoclonal gammapathies in Tunisia: epidemiological, immunochemical and etiological analysis of 288 cases].[突尼斯的单克隆丙种球蛋白病:288例病例的流行病学、免疫化学及病因学分析]
Pathol Biol (Paris). 2005 Feb;53(1):19-25. doi: 10.1016/j.patbio.2004.01.014.
5
The impact of M-component type and immunoglobulin concentration on the risk of malignant transformation in patients with monoclonal gammopathy of undetermined significance.M蛋白类型和免疫球蛋白浓度对意义未明的单克隆丙种球蛋白病患者恶性转化风险的影响。
Haematologica. 2001 Nov;86(11):1172-9.
6
Monoclonal and biclonal immunoglobulin-producing disorders.单克隆和双克隆免疫球蛋白生成障碍。
Eur J Haematol Suppl. 1989;51:11-8.
7
Proposal and validation of prognostic scoring systems for IgG and IgA monoclonal gammopathies of undetermined significance.意义未明的IgG和IgA单克隆丙种球蛋白病预后评分系统的提议与验证
Clin Cancer Res. 2009 Jul 1;15(13):4439-45. doi: 10.1158/1078-0432.CCR-08-3150. Epub 2009 Jun 9.
8
[Transient monoclonal gammopathies. Study of 34 cases].[短暂性单克隆丙种球蛋白病。34例病例研究]
Sangre (Barc). 1994 Oct;39(5):351-5.
9
[Monoclonal gammopathies in a series of 1683 plasma donors].[1683名血浆捐献者中的单克隆丙种球蛋白病]
Cas Lek Cesk. 2004;143(6):401-4; discussion 404.
10
Lymphoproliferative disorders in chronic hepatitis C.慢性丙型肝炎中的淋巴增殖性疾病
J Viral Hepat. 2004 Jul;11(4):302-9. doi: 10.1111/j.1365-2893.2004.00480.x.

引用本文的文献

1
Serum proteins and paraproteins in women with silicone implants and connective tissue disease: a case-control study.硅胶植入物与结缔组织病女性患者的血清蛋白和副蛋白:一项病例对照研究。
Arthritis Res Ther. 2007;9(5):R95. doi: 10.1186/ar2295.
2
Simultaneous analysis of serum immunoglobulins in patients with M protein using cellulose acetate membrane isoelectric focusing.使用醋酸纤维素膜等电聚焦法同时分析M蛋白患者的血清免疫球蛋白。
J Clin Lab Anal. 1999;13(4):145-50. doi: 10.1002/(sici)1098-2825(1999)13:4<145::aid-jcla2>3.0.co;2-c.