Albar Rawia, Mahdi Moaffaq, Alkeraithe Fawaz, Almufarriji Khalid Nawaf
King Saud bin Abdulaziz University for Health Sciences College of Medicine, Jeddah, Saudi Arabia.
Pediatric Department, King Abdulaziz Medical City, Jeddah, Saudi Arabia.
BMJ Case Rep. 2019 May 30;12(5):e227715. doi: 10.1136/bcr-2018-227715.
Severe combined immunodeficiency (SCID) is an extremely rare disease caused by a disruption in the forkhead box N1 () gene, with an incidence of <1 per 1 000 000 live births. We report a boy aged 4 months who presented with a history of fever for 3 weeks and enlarged lymph nodes. The fever was associated with dry cough and runny nose. On physical examination, we noted oral thrush, generalised lymphadenopathy, nail dystrophy and alopecia. Flow cytometry of lymph node biopsy showed high-grade B-cell lymphoma. In addition, Epstein-Barr virus (EBV) infection was documented by PCR. The diagnosis of SCID was made by genetic testing, which revealed a homozygous variant of the gene. The variant was confirmed with Sanger sequencing. Management of EBV infection and lymphoma was initiated; unfortunately, the patient passed away on day 45 of hospitalisation.
重症联合免疫缺陷病(SCID)是一种极其罕见的疾病,由叉头框N1()基因的破坏引起,活产发病率低于百万分之一。我们报告一名4个月大的男孩,有3周发热病史且淋巴结肿大。发热伴有干咳和流涕。体格检查时,我们发现有口腔念珠菌病、全身淋巴结病、指甲营养不良和脱发。淋巴结活检的流式细胞术显示为高级别B细胞淋巴瘤。此外,通过聚合酶链反应(PCR)证实存在爱泼斯坦-巴尔病毒(EBV)感染。通过基因检测做出了SCID的诊断,结果显示该基因存在纯合变异。该变异通过桑格测序得到确认。开始了对EBV感染和淋巴瘤的治疗;不幸的是,患者在住院第45天去世。