极低出生体重儿莫氏菌菌血症并发腹膜炎1例。

IF 0.8 Q4 PEDIATRICS
AJP Reports Pub Date : 2021-04-01 Epub Date: 2021-08-19 DOI:10.1055/s-0041-1732407
Betty Pham, Anne Denslow, Michel Mikhael, Jina Lim
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引用次数: 1

摘要

我们描述了一例迟发性莫氏摩根菌脓毒症在一个极低出生体重的男性新生儿出生在23和4/7周胎龄一个30岁的原孕母亲由于早产。母亲在其他方面都很健康,产前过程也很正常。她在分娩前接受了类固醇和氨苄西林治疗。虽然最初的血培养是阴性的,但在出生第4天,新生儿出现了脓毒症的迹象,包括白细胞增多和贫血,随后的血培养显示出莫氏分枝杆菌的生长。患者在出生第8天发生自发性肠穿孔,腹膜培养生长莫氏分枝杆菌。婴儿对标准治疗有反应,存活至出院,在门诊随访时几乎没有轻微的发育迟缓。虽然莫氏分枝杆菌已在新生儿人群中得到证实,但它通常会导致早发性败血症,并与早产儿的高死亡率有关。在这里,我们提出了这例迟发性新生儿脓毒症与莫氏分枝杆菌合并自发性肠穿孔,与生存的23周妊娠婴儿。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Case of an Extremely Low Birth Weight Infant with <i>Morganella morganii</i> Bacteremia and Peritonitis.

A Case of an Extremely Low Birth Weight Infant with Morganella morganii Bacteremia and Peritonitis.

We describe a case of late onset Morganella morganii sepsis in an extremely low birth weight male neonate born at 23 and 4/7 weeks gestational age to a 30-year-old primigravid mother due to preterm labor. The mother was otherwise healthy with an unremarkable prenatal course. She received steroids and ampicillin prior to delivery. While initial blood cultures were negative, at day of life 4, the neonate developed signs of sepsis with leukocytosis and bandemia, and subsequent blood culture demonstrated growth of M. morganii . The patient then had spontaneous intestinal perforation on day of life 8 with peritoneal cultures growing M. morganii . The infant responded to standard therapy and survived to discharge, with few mild developmental delays upon outpatient follow-up. While M. morganii has been demonstrated in the neonatal population, it generally causes early onset sepsis and is associated with high mortality in preterm neonates. Here, we present this case of late onset neonatal sepsis with M. morganii complicated by spontaneous intestinal perforation, with survival in a 23 weeks gestation infant.

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来源期刊
AJP Reports
AJP Reports PEDIATRICS-
CiteScore
2.20
自引率
0.00%
发文量
30
审稿时长
12 weeks
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