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

被引:0
|
作者
Xu, Jiuyang [1 ,2 ,3 ,4 ,5 ]
Wang, Yan [1 ,2 ,3 ,4 ,5 ]
Zhang, Yuan [6 ]
Zhai, Tianshu [1 ,2 ,3 ,4 ,5 ]
Li, Zhenling [7 ]
Zhong, Dingrong [8 ]
Cao, Bin [1 ,2 ,3 ,4 ,5 ]
Cui, Xiaojing [1 ,2 ,3 ,4 ,5 ]
机构
[1] China Japan Friendship Hosp, Natl Ctr Resp Med, Beijing 100029, Peoples R China
[2] China Japan Friendship Hosp, State Key Lab Resp Hlth & Multimorbid, Beijing 100029, Peoples R China
[3] China Japan Friendship Hosp, Natl Clin Res Ctr Resp Dis, Beijing 100029, Peoples R China
[4] Chinese Acad Med Sci, China Japan Friendship Hosp, Inst Resp Med, Beijing 100029, Peoples R China
[5] China Japan Friendship Hosp, Ctr Resp Med, Dept Pulm & Crit Care Med, 2 East Yinghua Rd, Beijing 100029, Peoples R China
[6] Beijing Hosp Tradit Chinese Med, Dept Resp Med, Beijing, Peoples R China
[7] China Japan Friendship Hosp, Dept Hematol, Beijing, Peoples R China
[8] China Japan Friendship Hosp, Dept Radiol, 2 East Yinghua Rd, Beijing 100029, Peoples R China
关键词
X-linked lymphoproliferative disease; Epstein-Barr virus; Non-Langerhans histiocytosis; Hemophagocytic lymphohistiocytosis; Pulmonary infection; MUTATIONS; EBV; DEFICIENCY; GENE; XLP;
D O I
10.1186/s12879-024-10281-8
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
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.
引用
收藏
页数:8
相关论文
共 50 条
  • [41] X-linked lymphoproliferative syndrome in mainland China: review of clinical, genetic, and immunological characteristic
    Xu, Tao
    Zhao, Qin
    Li, Wenyan
    Chen, Xuemei
    Xue, Xiuhong
    Chen, Zhi
    Du, Xiao
    Bai, Xiaoming
    Zhao, Qian
    Zhou, Lina
    Tang, Xuemei
    Yang, Xi
    Kanegane, Hirokazu
    Zhao, Xiaodong
    EUROPEAN JOURNAL OF PEDIATRICS, 2020, 179 (02) : 327 - 338
  • [42] Preimplantation Genetic Testing for a Chinese Family With X-Linked Lymphoproliferative Syndrome Type 1
    Chen, Songchang
    Shi, Weihui
    Qian, Yeqing
    Wang, Liya
    Zhang, Junyu
    Li, Shuyuan
    Chen, Yiyao
    Chang, Chunxin
    Fei, Hongjun
    Zhang, Lanlan
    Huang, Hefeng
    Xu, Chenming
    FRONTIERS IN GENETICS, 2020, 11
  • [43] Adult-onset Alexander disease
    Balbi, Pietro
    Seri, Marco
    Ceccherini, Isabella
    Uggetti, Carla
    Casale, Roberto
    Fundaro, Cira
    Caroli, Francesco
    Santoro, Lucio
    JOURNAL OF NEUROLOGY, 2008, 255 (01) : 24 - 30
  • [44] 1ST PRENATAL-DIAGNOSIS OF X-LINKED LYMPHOPROLIFERATIVE DISEASE
    SKARE, J
    MADAN, S
    GLASER, J
    PURTILO, D
    NITOWSKY, H
    PULIJAAL, V
    MILUNSKY, A
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 44 (01): : 79 - 81
  • [45] Different Phenotypic Presentations of X-Linked Lymphoproliferative Disease in Siblings with Identical Mutations
    Zohreh Nademi
    Nesrine Radwan
    Kanchan Rao
    Kimberly Gilmour
    Austen Worth
    Claire Booth
    Journal of Clinical Immunology, 2019, 39 : 523 - 526
  • [46] Maternal onset de novo SH2D1A mutation and lymphocytic choriomeningitis virus infection in a patient with X-linked lymphoproliferative disease type 1: A case report
    Liu, Jinrong
    Tian, Wenjun
    Wang, Fang
    Teng, Wen
    Zhang, Yang
    Tong, Chunrong
    Zhang, Chonglin
    Ju, Ying
    Zhang, Bingchang
    Zhao, Shunying
    Liu, Hongxing
    MOLECULAR MEDICINE REPORTS, 2015, 11 (05) : 3291 - 3294
  • [47] Deficiency of the proapoptotic SAP function in X-linked lymphoproliferative disease aggravates Epstein-Barr virus (EBV) induced mononucleosis and promotes lymphoma development
    Nagy, Noemi
    Klein, Eva
    IMMUNOLOGY LETTERS, 2010, 130 (1-2) : 13 - 18
  • [48] X-linked lymphoproliferative disease associated with hypogammaglobulinemia and growth-hormone deficiency
    Alangari, A
    Abobaker, A
    Kanegane, H
    Miyawaki, T
    EUROPEAN JOURNAL OF PEDIATRICS, 2006, 165 (03) : 165 - 167
  • [49] X-linked lymphoproliferative syndrome associated with Epstein-Barr virus encephalitis and lymphoproliferative disorder
    Mukai, Takeo
    Waki, Kenji
    CLINICAL CASE REPORTS, 2023, 11 (09):
  • [50] Different Phenotypic Presentations of X-Linked Lymphoproliferative Disease in Siblings with Identical Mutations
    Nademi, Zohreh
    Radwan, Nesrine
    Rao, Kanchan
    Gilmour, Kimberly
    Worth, Austen
    Booth, Claire
    JOURNAL OF CLINICAL IMMUNOLOGY, 2019, 39 (05) : 523 - 526