Kim Seul-Ki, Kim Min Chae, Han Seung Beom, Kim Seong Koo, Lee Jae Wook, Chung Nack-Gyun, Cho Bin, Jeong Dae Chul, Kang Jin Han, Kim Hack-Ki
Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul, Korea.; The Vaccine Bio Research Institute, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Blood Res. 2016 Dec;51(4):249-255. doi: 10.5045/br.2016.51.4.249. Epub 2016 Dec 23.
Although intravenous acyclovir therapy is recommended for varicella zoster virus (VZV) infection in immunocompromised children, the clinical characteristics and outcomes of VZV infection in the acyclovir era have rarely been reported.
The medical records of children diagnosed with varicella or herpes zoster virus, who had underlying hematologic malignancies, were retrospectively reviewed, and the clinical characteristics and outcomes of VZV infection were evaluated.
Seventy-six episodes of VZV infection (herpes zoster in 57 and varicella in 19) were identified in 73 children. The median age of children with VZV infection was 11 years (range, 1-17), and 35 (46.1%) episodes occurred in boys. Acute lymphoblastic leukemia was the most common underlying malignancy (57.9%), and 90.8% of the episodes occurred during complete remission of the underlying malignancy. Acyclovir was administered for a median of 10 days (range, 4-97). Severe VZV infection occurred in 16 (21.1%) episodes. Although the finding was not statistically significant, a previous history of hematopoietic cell transplantation (HCT) appeared to be associated with the development of more severe episodes of herpes zoster (=0.075).
Clinical characteristics of VZV infection in immunocompromised children were not significantly different from those without it, and clinical outcomes improved after the introduction of acyclovir therapy. However, risk factors for severe VZV infection require further investigation in a larger population and a prospective setting.
尽管推荐对免疫功能低下的儿童采用静脉注射阿昔洛韦治疗水痘带状疱疹病毒(VZV)感染,但在阿昔洛韦时代,VZV感染的临床特征和结局鲜有报道。
对诊断为水痘或带状疱疹病毒感染且患有血液系统恶性肿瘤的儿童的病历进行回顾性分析,评估VZV感染的临床特征和结局。
在73名儿童中发现了76例VZV感染(57例为带状疱疹,19例为水痘)。VZV感染儿童的中位年龄为11岁(范围1 - 17岁),35例(46.1%)发生在男孩中。急性淋巴细胞白血病是最常见的潜在恶性肿瘤(57.9%),90.8%的感染发生在潜在恶性肿瘤的完全缓解期。阿昔洛韦的中位给药时间为10天(范围4 - 97天)。16例(21.1%)发生了严重的VZV感染。虽然这一发现无统计学意义,但既往造血细胞移植(HCT)史似乎与更严重的带状疱疹发作有关(P = 0.075)。
免疫功能低下儿童VZV感染的临床特征与非免疫功能低下儿童无显著差异,阿昔洛韦治疗引入后临床结局有所改善。然而,严重VZV感染的危险因素需要在更大规模人群和前瞻性研究中进一步调查。