Latvian Biomedical Research and Study Centre, Ratsupites Str 1, k-1, Riga, LV-1067, Latvia.
Riga East University Hospital, Centre of Tuberculosis and Lung Diseases, Upeslejas, Stopiņi region, LV-2118, Latvia.
BMC Infect Dis. 2020 Feb 5;20(1):105. doi: 10.1186/s12879-020-4832-3.
Urogenital tuberculosis (TB) is rare in children and usually develops due to reactivation of the foci in the genitourinary tract after the latency period following initial infection. Urogenital TB in children has no pathognomonic clinical features that can result in overlooking or misdiagnosing this clinical entity. Here, we report important findings regarding the pathogenesis and transmission of TB by using genotyping and whole-genome sequencing (WGS) in a study of renal TB case in a child.
A 13-year-old boy was admitted to the hospital because of high fever, severe dry cough, flank pain and painful urination. Abdominal ultrasonography and CT revealed an 8 mm calculus in the kidney, and clinical findings were initially interpreted as nephrolithiasis. Nevertheless, due to the atypical clinical presentation of kidney stone disease, additional investigations for possible TB were performed. The QuantiFERON®-TB Gold Plus test was positive, and the Mantoux test resulted in 15 mm of induration, confirming infection with Mycobacterium tuberculosis (Mtb). Chest X-ray was normal. Chest CT revealed calcified intrathoracic lymph nodes. The urine sample tested positive for acid-fast bacilli, and Mtb cultures were obtained from urine and bronchial aspirate samples, resulting in a final diagnosis of intrathoracic lymph node and renal TB. Contact investigation revealed that the child's father was diagnosed with TB when the child was 1 year old. Genotyping and WGS analysis of Mtb isolates of the child and his father confirmed the epidemiological link and pointed to the latency of infection in the child.
This case report confirmed the development of active TB from calcified lesions in adolescent after 12 years of exposure, demonstrated the absence of microevolutionary changes in the Mtb genome during the period of latency, and proved the importance of appropriate evaluation and management to prevent the progression of TB infection to active TB disease. The use of WGS provided the ultimate resolution for the detection of TB transmission and reactivation events.
泌尿生殖系统结核(TB)在儿童中较为罕见,通常是在初次感染后潜伏期内,泌尿生殖系统内的病灶重新激活所致。儿童泌尿生殖系统 TB 没有特征性的临床特征,可能导致对此临床实体的忽视或误诊。在这里,我们通过对一例儿童肾 TB 病例进行基因分型和全基因组测序(WGS)研究,报告了关于 TB 发病机制和传播的重要发现。
一名 13 岁男孩因高热、剧烈干咳、腰痛和尿痛而入院。腹部超声和 CT 显示肾脏有 8mm 的结石,临床发现最初被解读为肾结石。然而,由于肾结石疾病的临床表现不典型,因此进行了可能的 TB 额外检查。QuantiFERON®-TB Gold Plus 检测呈阳性,Mantoux 试验硬结 15mm,证实感染了结核分枝杆菌(Mtb)。胸部 X 线正常。胸部 CT 显示钙化性胸内淋巴结。尿液样本抗酸杆菌检测阳性,尿液和支气管抽吸物样本中均获得 Mtb 培养物,最终诊断为胸内淋巴结和肾 TB。接触调查显示,孩子的父亲在孩子 1 岁时被诊断出患有 TB。对孩子及其父亲的 Mtb 分离株进行基因分型和 WGS 分析证实了流行病学联系,并指出孩子存在感染潜伏期。
本病例报告证实了青少年在暴露 12 年后从钙化病灶中发展为活动性 TB,证明了 Mtb 基因组在潜伏期内没有微进化变化,并证明了适当评估和管理以防止 TB 感染进展为活动性 TB 疾病的重要性。WGS 的使用为检测 TB 传播和再激活事件提供了最终解决方案。