A case of adult-onset X-linked lymphoproliferative disease mimicking pulmonary infection

X-linked lymphoproliferative disease (XLP) is a rare primary immunodeficiency with susceptibility and vulnerability to Epstein-Barr virus (EBV) infection. Most patients were diagnosed in early childhood and do not survive into adulthood. Here we reported an adult-onset XLP patient presenting with fever, dyspnea, and pulmonary nodules, mimicking respiratory infection at disease onset. Diagnosis was made based on whole-exon sequencing and pedigree analysis. Chest CT showed bilateral nodular lesions partially responsive to steroid therapy. The symptoms were managed with high-dose steroid, together with broad-spectrum anti-infective treatment for mixed secondary opportunistic infections. Pathology studies revealed non-Langerhans histiocytosis and T cell infiltration in lungs. Our case highlights the importance of genetic sequencing in managing young patients with unexplained infection and potential immuno-deficiency. We also added to the understanding of XLP by carrying detailed investigation into the pulmonary lesions.

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Publication Details

Journal
BMC Infectious Diseases
Published
2024-12-18
DOI
https://doi.org/10.1186/s12879-024-10281-8
Primary Topic
Viral-associated cancers and disorders
Type
article
Field-Weighted Citation Impact
0.00

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article

A case of adult-onset X-linked lymphoproliferative disease mimicking pulmonary infection

Zhenling Li, Jiuyang Xu, Dingrong Zhong, Yuan Zhang et al.
BMC Infectious Diseases
Viral-associated cancers and disorders
article

A case of adult-onset X-linked lymphoproliferative disease mimicking pulmonary infection

Zhenling Li, Jiuyang Xu, Dingrong Zhong, Yuan Zhang, Xiaojing Cui, Bin Cao, Tianshu Zhai, Yan Wang
article en

Abstract

X-linked lymphoproliferative disease (XLP) is a rare primary immunodeficiency with susceptibility and vulnerability to Epstein-Barr virus (EBV) infection. Most patients were diagnosed in early childhood and do not survive into adulthood. Here we reported an adult-onset XLP patient presenting with fever, dyspnea, and pulmonary nodules, mimicking respiratory infection at disease onset. Diagnosis was made based on whole-exon sequencing and pedigree analysis. Chest CT showed bilateral nodular lesions partially responsive to steroid therapy. The symptoms were managed with high-dose steroid, together with broad-spectrum anti-infective treatment for mixed secondary opportunistic infections. Pathology studies revealed non-Langerhans histiocytosis and T cell infiltration in lungs. Our case highlights the importance of genetic sequencing in managing young patients with unexplained infection and potential immuno-deficiency. We also added to the understanding of XLP by carrying detailed investigation into the pulmonary lesions.

BMC Infectious DiseasesVol. 24(1)
Chinese Academy of Medical Sciences & Peking Union Medical College (CN), China-Japan Friendship Hospital (CN), Beijing Hospital of Traditional Chinese Medicine (CN)
Chinese Academy of Medical Sciences, China-Japan Friendship Hospital
Good health and well-being
Openalex Percentile: Top 59%
Viral-associated cancers and disorders
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