Xu Jiuyang, Wang Yan, Zhang Yuan, Zhai Tianshu, Li Zhenling, Zhong Dingrong, Cao Bin, Cui Xiaojing
National Center for Respiratory Medicine, China-Japan Friendship Hospital, Beijing, 100029, China.
State Key Laboratory of Respiratory Health and Multimorbidity, China-Japan Friendship Hospital, Beijing, 100029, China.
BMC Infect Dis. 2024 Dec 18;24(1):1399. doi: 10.1186/s12879-024-10281-8.
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.
X连锁淋巴增殖性疾病(XLP)是一种罕见的原发性免疫缺陷病,易受爱泼斯坦-巴尔病毒(EBV)感染。大多数患者在幼儿期被诊断出来,无法存活至成年。在此,我们报告了一名成年发病的XLP患者,其最初表现为发热、呼吸困难和肺结节,类似呼吸道感染。诊断基于全外显子测序和家系分析。胸部CT显示双侧结节性病变,对类固醇治疗部分有效。症状通过大剂量类固醇治疗以及针对混合性继发性机会性感染的广谱抗感染治疗得以控制。病理研究显示肺部存在非朗格汉斯组织细胞增多症和T细胞浸润。我们的病例强调了基因测序在管理不明原因感染和潜在免疫缺陷的年轻患者中的重要性。通过对肺部病变进行详细调查,我们也增进了对XLP的了解。