Suppr超能文献

类风湿关节炎合并中性粒细胞减少患者中颗粒淋巴细胞增殖的患病率。

Prevalence of granular lymphocyte proliferation in patients with rheumatoid arthritis and neutropenia.

作者信息

Saway P A, Prasthofer E F, Barton J C

机构信息

Department of Medicine, Multipurpose Arthritis Center, University of Alabama, Birmingham.

出版信息

Am J Med. 1989 Mar;86(3):303-7. doi: 10.1016/0002-9343(89)90300-8.

Abstract

PURPOSE

Granular lymphocyte proliferation and neutropenia with or without splenomegaly occurs with unknown frequency in rheumatoid arthritis. We decided to evaluate the prevalence of Felty's syndrome and granular lymphocyte proliferation among patients with rheumatoid arthritis and to determine the fraction of patients with granular lymphocyte proliferation who also had rheumatoid arthritis.

PATIENTS, METHODS, AND RESULTS: We retrospectively analyzed 1,053 cases of rheumatoid arthritis and 13,505 marrow examination reports for the decade 1978 to 1987. Among patients with Felty's syndrome rheumatoid arthritis with neutropenia/leukopenia, and rheumatoid arthritis with splenomegaly, we identified 18 patients with neutropenia as a manifestation of rheumatoid arthritis. We also identified marrow examinations in 150 patients with rheumatoid arthritis. Using blood counts, microscopy of marrow, and surface antigen analysis of mononuclear cells, we determined that 12 patients had typical Felty's syndrome and six had granular lymphocyte proliferation, representing prevalences of 1.1 percent and 0.6 percent, respectively. No patient had granular lymphocyte proliferation without neutropenia.

CONCLUSION

Granular lymphocyte proliferation and neutropenia with or without splenomegaly in rheumatoid arthritis commonly resembles typical Felty's syndrome. Further, the six patients with granular lymphocyte proliferation represent 20 percent of our institution's patients with granular lymphocyte proliferation, supporting the previously described common association of this disorder with rheumatoid arthritis. The relatively large fraction of deaths (due to malignancy and infection) among the patients with typical Felty's syndrome suggests that their mean survival may be comparatively less than in those with granular lymphocyte proliferation.

摘要

目的

类风湿关节炎患者中,粒细胞淋巴细胞增殖伴或不伴脾肿大以及中性粒细胞减少的发生频率尚不清楚。我们决定评估类风湿关节炎患者中费尔蒂综合征和粒细胞淋巴细胞增殖的患病率,并确定同时患有类风湿关节炎的粒细胞淋巴细胞增殖患者的比例。

患者、方法与结果:我们回顾性分析了1978年至1987年这十年间的1053例类风湿关节炎病例和13505份骨髓检查报告。在患有费尔蒂综合征(类风湿关节炎伴中性粒细胞减少/白细胞减少)和类风湿关节炎伴脾肿大的患者中,我们确定了18例以中性粒细胞减少为类风湿关节炎表现的患者。我们还确定了150例类风湿关节炎患者的骨髓检查情况。通过血细胞计数、骨髓显微镜检查和单核细胞表面抗原分析,我们确定12例患者患有典型的费尔蒂综合征,6例患有粒细胞淋巴细胞增殖,患病率分别为1.1%和0.6%。没有患者在无中性粒细胞减少的情况下出现粒细胞淋巴细胞增殖。

结论

类风湿关节炎中粒细胞淋巴细胞增殖伴或不伴脾肿大以及中性粒细胞减少通常类似于典型的费尔蒂综合征。此外,6例粒细胞淋巴细胞增殖患者占我们机构粒细胞淋巴细胞增殖患者的20%,支持了此前描述的这种疾病与类风湿关节炎的常见关联。典型费尔蒂综合征患者中相对较高的死亡比例(由于恶性肿瘤和感染)表明,他们的平均生存期可能比粒细胞淋巴细胞增殖患者相对更短。

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