Suppr超能文献

一名新生儿培养出B族链球菌CPS III血清型阳性菌株,出现复发性败血症和神经侵袭性疾病。

Recurrent sepsis and neuroinvasive disease in a neonate culture-positive for a Group B Streptococcus CPS III serotype, + strain.

作者信息

Suresh Sneha, Tyrrell Gregory, Alhhazmi Areej, Escoredo Sandra, Hawkes Michael

机构信息

University of Alberta , Edmonton , Canada.

出版信息

JMM Case Rep. 2016 Jun 25;3(3):e005034. doi: 10.1099/jmmcr.0.005034. eCollection 2016 Jun.

Abstract

INTRODUCTION

Late-onset disease with Group B Streptococcus (GBS LOD) remains a significant problem in neonates. Unlike early-onset disease, rates of GBS LOD have not changed with prenatal testing. Effects of GBS LOD can be severe and thus identifying risk factors for severe GBS LOD, such as hypervirulence genes, may help in managing these infants.

CASE PRESENTATION

We present a case of a neonate with capsular serotype III GBS sepsis without meningitis that recurred 6 days after a 10-day-treatment period with IV ampicillin. The second episode was characterized by sepsis, neuroinvasion, meningitis and subsequent profound encephalomalacia. The short duration between the two episodes suggested recrudescence rather than reinfection. The GBS isolate was ultimately found to be positive for hypervirulence gene , which encodes for a protein known to mediate meningeal tropism and neuroinvasion.

CONCLUSION

positivity may thus potentially serve as an important biomarker for severe and neuroinvasive GBS LOD that can influence treatment decisions.

摘要

引言

B族链球菌所致迟发性疾病(GBS LOD)在新生儿中仍然是一个重大问题。与早发性疾病不同,GBS LOD的发病率并未因产前检测而改变。GBS LOD的影响可能很严重,因此识别严重GBS LOD的危险因素,如高毒力基因,可能有助于对这些婴儿进行管理。

病例报告

我们报告一例新生儿,患有III型荚膜GBS败血症但无脑膜炎,在接受静脉注射氨苄西林治疗10天后,6天复发。第二次发作的特征为败血症、神经侵袭、脑膜炎及随后的严重脑软化。两次发作之间的时间间隔较短,提示为复发而非再感染。最终发现该GBS分离株的高毒力基因呈阳性,该基因编码一种已知可介导脑膜嗜性和神经侵袭的蛋白质。

结论

因此,阳性可能潜在地作为严重和神经侵袭性GBS LOD的重要生物标志物,可影响治疗决策。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f76b/5330226/4a54fdecc0fc/jmmcr-03-5034-f001.jpg

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