Suppr超能文献

[原发性骨髓增生异常综合征。预后因素以及单克隆和多克隆丙种球蛋白病的频繁出现]

[Primary myelodysplastic syndrome. Prognostic factors and frequent appearance of monoclonal and polyclonal gammopathies].

作者信息

von Hirschhausen R, Saal J G

机构信息

Abteilung Innere Medizin II, Medizinische Klinik und Poliklinik der Universität Tübingen.

出版信息

Dtsch Med Wochenschr. 1990 Jan 19;115(3):88-92.

PMID:2298125
Abstract

Prognostic factors were obtained by retrospective analysis of data on 44 patients (34 men and ten women; average age 64 +/- 13 years) with a primary myelodysplastic syndrome. The most important factors for a poor prognosis were the presence of more than 5% blast cells in the bone marrow (P = 0.001), serum platelet count of less than 150,000/microliters (P = 0.05), serum white cell count less than 3000/microliters (not significant) and serum lactate dehydrogenase concentration greater than 240 U/l (P = 0.05). Protein electrophoresis revealed a polyclonal hypergammaglobulinaemia in 15 of 38 patients; in eight of 17 patients with partly normal curve pattern at protein electrophoresis, a monoclonal gammopathy was demonstrated (monoclonal gradient 3.5 g/dl) by immunoelectrophoresis or immunofixation. No prognostic significance could be established for these gammopathies.

摘要

通过对44例原发性骨髓增生异常综合征患者(34例男性和10例女性;平均年龄64±13岁)的数据进行回顾性分析,得出预后因素。预后不良的最重要因素是骨髓中原始细胞超过5%(P = 0.001)、血清血小板计数低于150,000/微升(P = 0.05)、血清白细胞计数低于3000/微升(无统计学意义)以及血清乳酸脱氢酶浓度高于240 U/l(P = 0.05)。蛋白电泳显示,38例患者中有15例出现多克隆高球蛋白血症;在17例蛋白电泳曲线部分正常的患者中,有8例通过免疫电泳或免疫固定法显示出单克隆丙种球蛋白病(单克隆梯度为3.5 g/dl)。这些丙种球蛋白病未显示出预后意义。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验