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A family history of serious complications due to BCG vaccination is a tool for the early diagnosis of severe primary immunodeficiency

机译:由卡介苗接种引起的严重并发症的家族史是早期诊断严重原发性免疫缺陷的工具

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摘要

Severe Combined Immunodeficiency (SCID) is one of the most severe forms of primary immunodeficiency (PID). Complications of BCG vaccination, especially disseminated infection and its most severe forms, are known to occur in immunodeficient patients, particularly in SCID. A carefully taken family history before BCG injection as well as delaying vaccination if PID is suspected could be a simple and effective method to avoid inappropriate vaccination of an immunodeficient child in some cases until the prospect of newborn screening for SCID has been fully developed. We describe a patient with a very early diagnosis of SCID, which was suspected on the basis of the previous death of two siblings younger than one year due to severe complications secondary to the BCG vaccine. We suggest that a family history of severe or fatal reactions to BCG should be included as a warning sign for an early diagnosis of SCID.
机译:严重的免疫缺陷综合症(SCID)是原发性免疫缺陷(PID)的最严重形式之一。已知BCG疫苗接种的并发症,尤其是弥漫性感染及其最严重的形式,发生在免疫缺陷患者中,尤其是在SCID中。在某些情况下,直到对SCID进行新生儿筛查的可能性得到充分发展之前,在BCG注射之前仔细检查家族史以及如果怀疑PID可能会延迟疫苗接种可能是避免某些免疫缺陷儿童接种不当疫苗的简单有效的方法。我们描述了一名患有SCID的早期诊断的患者,该患者被怀疑是由于BCG疫苗继发的严重并发症而导致两名不到一年的兄弟姐妹先前死亡。我们建议应将对卡介苗有严重或致命反应的家族病史作为早期诊断SCID的警告信号。

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