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链球菌性肺炎脑膜炎作为X连锁无丙种球蛋白血症的首发表现:一例报告及讨论

Streptococcal pneumonia meningitis as an initial presentation of X-linked agammaglobulinemia: A case report and discussion.

作者信息

Kadden Daniel, Fowler Grace, Engel Elissa, Logan Casey, Marathe Kalyani, Gosdin Craig

机构信息

UC College of Medicine, Department of Pediatrics Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA.

出版信息

J Am Coll Emerg Physicians Open. 2021 Sep 17;2(5):e12553. doi: 10.1002/emp2.12553. eCollection 2021 Oct.

Abstract

X-linked agammaglobulinemia (XLA) is a primary immunodeficiency caused by mutations in the gene for Bruton's tyrosine kinase , with affected males most commonly presenting with recurrent bacterial infections during the first few years of life. Here we present a 17-month-old male with a chief complaint of worsening rash and fever, whose history of streptococcal pneumonia meningitis at 5 months of age prompted suspicion for an underlying immunodeficiency and subsequent diagnosis of XLA. Bacterial meningitis is a rare initial presentation of XLA, and therefore physicians may easily overlook any underlying immunodeficiency. Prompt workup for immunodeficiency should be initiated in any vaccinated patient with a history of pneumococcal meningitis outside of the newborn period. Further discussion surrounding the various presentations of XLA, their related clinical manifestations and laboratory findings, and the importance of thorough chart review may encourage earlier diagnosis and initiation of treatment of this disease.

摘要

X连锁无丙种球蛋白血症(XLA)是一种原发性免疫缺陷病,由布鲁顿酪氨酸激酶基因的突变引起,受影响的男性最常见的表现是在生命的最初几年反复发生细菌感染。在此,我们报告一名17个月大的男性,其主要诉求为皮疹和发热加重,他在5个月大时患链球菌性肺炎脑膜炎的病史引发了对潜在免疫缺陷的怀疑,随后被诊断为XLA。细菌性脑膜炎是XLA罕见的初始表现,因此医生可能很容易忽略任何潜在的免疫缺陷。对于任何在新生儿期以外有肺炎球菌脑膜炎病史的接种疫苗患者,都应及时进行免疫缺陷检查。围绕XLA的各种表现、其相关的临床表现和实验室检查结果以及全面病历审查的重要性展开进一步讨论,可能会促使更早地诊断和开始治疗这种疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1fb/8448482/831bddb4518f/EMP2-2-e12553-g001.jpg

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