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一名3岁儿童复发性极晚发性B族链球菌败血症的首例病例。

The first case of recurrent ultra late onset group B streptococcal sepsis in a 3-year-old child.

作者信息

Hosoda Ai, Gatayama Ryohei, Moriyama Shiori, Ishii Noriyuki, Yamada Kenichiro, Matsuzaki Youhei, Shinjoh Masayoshi

机构信息

Department of Pediatrics, Hiratsuka City Hospital, Kanagawa, Japan; Department of Pediatrics, Sano Kousei General Hospital, Tochigi, Japan.

Department of Pediatrics, Hiratsuka City Hospital, Kanagawa, Japan.

出版信息

IDCases. 2016 Nov 24;7:16-18. doi: 10.1016/j.idcr.2016.11.007. eCollection 2017.

Abstract

Group B streptococcus (GBS) is a commonly recognized cause of sepsis and meningitis in neonatal and young infants. Invasive GBS infection is classified into early onset GBS disease (EOD, day 0-6), late onset GBS disease (LOD, day 7-89) and ultra late onset GBS disease (ULOD, after 3 months of age). ULOD is uncommon and recurrence is especially rare. We present the first recurrent case of ULOD GBS sepsis in 3-year-old girl with a past medical history of hydrops fetalis and thoracic congenital lymphatic dysplasia. The first episode presented as sepsis at 2 years 8 months of age. The second episode occurred as sepsis with encephalopathy at 3 years 1 months of age. During each episode, the patient was treated using intravenous antimicrobials and her condition improved. Serotype examination was not performed in the first episode, but GBS type V was serotyped in the second episode. ULOD over 1 year of age is quite rare and may recur.

摘要

B族链球菌(GBS)是新生儿和幼儿败血症及脑膜炎的常见病因。侵袭性GBS感染分为早发型GBS疾病(EOD,第0 - 6天)、晚发型GBS疾病(LOD,第7 - 89天)和极晚发型GBS疾病(ULOD,3个月龄后)。ULOD并不常见,复发尤其罕见。我们报告了首例3岁女童复发性ULOD GBS败血症病例,该女童既往有胎儿水肿和胸段先天性淋巴管发育不良病史。首次发作表现为2岁8个月时的败血症。第二次发作发生在3岁1个月时,表现为败血症合并脑病。每次发作时,患者均接受静脉抗菌药物治疗,病情好转。首次发作时未进行血清型检测,但第二次发作时检测出GBS V型。1岁以上的ULOD非常罕见,且可能复发。

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本文引用的文献

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Group B streptococcal meningitis in a 5-year-old boy.一名5岁男孩的B族链球菌脑膜炎
Indian J Pediatr. 2003 Jun;70(6):509-11. doi: 10.1007/BF02723144.
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Invasive group B streptococcal disease in children beyond early infancy.婴儿早期过后儿童的侵袭性B族链球菌病
Pediatr Infect Dis J. 1995 Apr;14(4):278-81. doi: 10.1097/00006454-199504000-00006.
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