| Literature DB >> 32388558 |
Sai Hu Huang1, Xiang Ying Meng1, Zhen Jiang Bai1, Ying Li1, Shui Yan Wu1.
Abstract
We reported a Chinese boy with X-linked hyper IgM (XHIGM) syndrome, manifesting as recurrent and severe pneumonia caused by Pneumocystis jirovecii. His parents were healthy and unrelated. In August 2018, the 5-month-old boy manifested as cough and dyspnea, and then in July 2019, he was admitted because of the same symptoms. Immunological results of the two admissions both showed low IgG, low IgA, normal IgM and high levels of 1,3-β-D-glucan (BDG). Using next-generation sequencing (NGS), great reading counts of P. jirovecii were identified from the deep sputum in both admissions. Caspofungin combined with trimethoprim-sulfamethoxazole were used to anti-infection, and he recovered quickly. Whole-exome sequencing was performed for this family because of immune suppression, the disease-causing gene (exon 10-22 of CD40L) deletion for XHIGM syndrome was identified. NGS is beneficial for etiology diagnosis. Pneumocystis jirovecii pneumonia as an opportunistic infection could be recurrent in patients with XHIGM syndrome.Entities:
Keywords: zzm321990 Pneumocystis jirovecii pneumonia; X-linked hyper IgM syndrome; next-generation sequencing
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Year: 2020 PMID: 32388558 DOI: 10.1093/tropej/fmaa023
Source DB: PubMed Journal: J Trop Pediatr ISSN: 0142-6338 Impact factor: 1.165