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内脏异构和多脾症女孩的致死性肺炎球菌败血症:病例报告。

Fatal pneumococcal septicemia in a girl with visceral heterotaxy and polysplenia: a case report.

机构信息

Provincial Forensic Pathology Unit, Ontario Forensic Pathology Service, 25 Morton Shulman Avenue, Toronto, Ontario, M3M 0B1, Canada.

Department of Laboratory Medicine & Pathobiology, University of Toronto, Toronto, Canada.

出版信息

Forensic Sci Med Pathol. 2020 Sep;16(3):519-522. doi: 10.1007/s12024-020-00252-1. Epub 2020 May 13.

DOI:10.1007/s12024-020-00252-1
PMID:32405984
Abstract

We report an unusual case of a 15-month old previously healthy girl who died of pneumococcal septicemia in the background of visceral heterotaxy with polysplenia. Heterotaxy can also present with asplenia whereas polysplenia cases usually present with functional asplenia. Of particular note, this girl received the 13-valent pneumococcal conjugate vaccine as recommended by the Centers for Disease Control and Prevention in the routine pediatric immunization schedule used in the USA and Canada. Unfortunately, although the strain causing death (serotype 22F) is not contained in Prevnar 13®, it is in the 23-valent pneumococcal polysaccharide vaccine (e.g. Pneumovax 23®), currently suggested only for immunocompromised children age 2 with either functional or anatomic asplenia. This syndrome has the potential of being diagnosed prenatally. The intent of our case report is to raise awareness of the syndrome, highlight that heterotaxy patients with polysplenia are at danger for infections with encapsulated organism, such as pneumococcus, meningococcus, and Haemophilus influenza amongst others due to functional asplenia, recommend the 23-valent pneumococcal polysaccharide vaccine for these children before age two for the outlined reasons, and illustrate that with early diagnosis of the heterotaxy syndrome, and early diagnosis and treatment of septic complications, the morbidity or death of young children with heterotaxy syndrome can likely be reduced or prevented.

摘要

我们报告了一例不常见的病例,一名 15 个月大的既往健康女孩,患有内脏异构伴多脾,死于肺炎球菌败血症。异构症也可能表现为无脾,而多脾症通常表现为功能性无脾。值得特别注意的是,这名女孩按照美国和加拿大常规儿科免疫接种计划中疾病控制与预防中心的建议,接种了 13 价肺炎球菌结合疫苗。不幸的是,尽管导致死亡的菌株(血清型 22F)不在沛儿 13® 中,但它存在于 23 价肺炎球菌多糖疫苗(如沛儿 23®)中,目前仅建议 2 岁以下功能性或解剖性无脾的免疫功能低下儿童使用。这种综合征有可能在产前被诊断出来。我们报告这个病例的目的是提高对这种综合征的认识,强调由于功能性无脾,多脾的异构症患者存在感染带囊膜的病原体(如肺炎球菌、脑膜炎球菌和流感嗜血杆菌等)的危险,鉴于上述原因,建议这些儿童在 2 岁之前接种 23 价肺炎球菌多糖疫苗,并说明通过早期诊断异构症综合征以及早期诊断和治疗败血症并发症,可以降低或预防患有异构症综合征的幼儿的发病率或死亡率。

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