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Severe fever with thrombocytopenia syndrome in children: a case report
BMC Infectious Diseases volume 14, Article number: 366 (2014)
Severe fever with thrombocytopenia syndrome (SFTS) is an emerging infectious disease caused by a novel bunyavirus (SFTSV) in China. Humans of all ages living in endemic areas have high risk of acquiring SFTS. Most clinical data so far have been from adults and no clinical study was available from children yet. The present study identified four SFTSV infected children through hospital based surveillance. A prospective observational study was performed to obtain their clinical and laboratory characteristics.
The patients’ age ranged from 4–15 years old and two were male. On hospitalization, fever, malaise and gastrointestinal syndromes were the most commonly presenting symptoms. Hemorrhagic symptoms or neurological manifestation was not recorded in any of the four pediatric patients. Hematological abnormalities at admission into hospital included leucopenia (4 cases), thrombocytopenia (1 case) and bicytopenia (1 case). The abnormal parameters included elevated aminotransferase (1 case), alanine transaminase (2 case), and lactate dehydrogenase (3 case). Laboratory parameters indicative of renal damage was not observed during the hospitalization. All the patients recovered well without sequelae being observed.
Compared with adults, pediatric patients with SFTSV infection seem to have less vague subjective complaints and less aggressive clinical course. Thrombocytopenia is suggested to be used less rigorously in recognizing SFTSV infection in pediatric patients, especially at early phase of disease.
Severe fever with thrombocytopenia syndrome (SFTS) is an emerging infectious disease caused by a novel bunyavirus (SFTSV) that was firstly described in 2010 in China , Outside China, confirmed SFTS or SFTS like patients had recently been reported in Korea, Japan, Dubai, United Arab Emirates and Missouri, United States, suggesting its expanded distribution in other countries [2–5] The disease usually presents as fever, thrombocytopenia and leukocytopenia, with case-fatality rates ranging from 2.5% to 30% . Epidemiological investigation revealed that SFTS cases mostly lived in rural areas working as farmers, and their age ranged from 1 to 90, with most part of cases (75%) older than 50 years old [1, 5, 6]. Although pediatric patients under 18 years old were recorded, most data available so far have been from adults and no clinical study on children was performed yet.
Since 2011, we have performed a hospital based surveillance on SFTSV infected cases in one SFTS-designated hospital in Xinyang, Henan Province, China . From the same hospital, we identified four pediatric cases confirmed to be infected with SFTSV by real-time reverse transcriptase polymerase chain reaction (RT-PCR) and subsequent sequencing . A prospective observational study was performed to obtain their clinical and laboratory characteristics from acute phase of infection until convalescence. Altogether 180 SFTSV infected adult patients who had been hospitalized during the same period from the same hospital were extracted for comparison with these pediatric patients.
The median age of the pediatric patients was 8 (range 4–15) years old and 2 were male. Two of the patients had tick bite history during their outdoor activity. The other two had close contacts with their SFTSV infected family members, which is a higher frequency than in adults (6.7%). All the pediatric patients were otherwise healthy and had no previous co-morbidity. The delay from disease onset to hospital entrance was 3–7 days, comparable with that of adults (mean 5 days). On hospitalization, fever, malaise and gastrointestinal syndromes were the most commonly presenting symptoms. This is similar with the results that were obtained from adult patients (Table 1). No syndromes of dyspnea, headache, consciousness disorder, dizziness, sputum production, cough or myalgias were observed from the pediatric patients, which were presented with frequencies ranging from 11.7% to 82.2% in adult patients. Hemorrhagic symptoms (hematuria, petechia, hematemesis, gingival bleeding, melena), which were manifested in adult patients were rarely found in these pediatric patients, except for the presence of petechia in case 1. No neurological manifestation was recorded in any of the four pediatric patients.
For the laboratory tests, hematological abnormalities at admission into hospital included leucopenia (4 cases), thrombocytopenia (1 case) and bicytopenia (1 case). The abnormal parameters indicative of liver damage, for example, aspartate aminotransferase (AST), alanine transaminase (ALT), and lactate dehydrogenase (LDH) were presented in one, two and three patients, respectively. The frequencies in adults ranged from 63.9% (ALT) to 82.2% (AST). None of the pediatric patients had elevated albumin (ALB), blood urea nitrogen (BUN), creatinine (CREA), or presence of proteinuriay, which were mostly indicative of renal damage. These abnormalities were present in 45.6%, 25%, 22.8% and 30.6% among adult patients, respectively. At the end of clinical course, all patients presented different degree of neutropenia.
The pediatric patients had peak temperature of 38.8°C after hospitalization, declining to normal level at 4–8 days post disease onset. In contrast, the estimated median fever course in adult patients was 2 days (Figure 1A). The dynamic evaluations of PLT revealed a delayed occurrence of thrombocytopenia in three patients (5–6 days after disease onset) than that of the adults (mean 1–2 days). In addition, the recovery of PLT to normal levels was earlier than that of the adults (5–9 vs 10 days). The nadir levels of WBC counts in all the 4 children were lower than the mean level of adults at the same time points post infection, yet with a more rapid recovery than that of adults in case 1, 2 and 4 (Figure 1C).For the other four abnormal indicators, AST and CK were maintained at significantly lower level than the adults (Figure 1C and G), and case 1 additionally had lower level of ALT (Figure 1E). Similar patterns were observed between pediatric and adult patients for other evaluations (Figure 1D-G). It’s noteworthy that for case 3 and case 4, ALT and AST levels were normal on admission, only elevated to abnormal during the follow-up period. During the whole hospitalization, all the pediatric patients had normal BUN, CREA and ALB levels and no hemorrhagic symptoms other than petechia developed (data not shown).
At 2-month revisit to the hospital, the patients remained healthy without sequelae. patient 2 and patient 3 developed antibody titers of 1:160 and 1:640 by enzyme-linked immunosorbent assay (ELISA) using the recombinant nucleoprotein of SFTSV . In comparison, the IgG antibody titers of their household members from whom the infection was acquired were both 1:320. The other two pediatric patients failed to be revisited on the 2-month revisit.
Discussion and conclusions
In the current study, no death occurred among 4 pediatric patients and their clinical manifestation appeared to be milder than those of the adult patients. Apart from fever and gastrointestinal syndromes, the pediatric patients presented with less vague subjective complaints, as well as rare hemorrhagic symptom which were more often presented in adult patients. This made the recognition of pediatric SFTS cases more difficult than the adults, solely based on clinical syndromes. According to the original diagnosis criteria, a clinical SFTS patient was defined as presenting both thrombocytopenia and lymphopenia . However, thrombocytopenia is not evident until several days after hospitalization according to the current finding from pediatric patients. These patients might be missed if diagnosed by the standard criteria. We therefore propose that thrombocytopenia should be used less rigorously in recognizing SFTSV infection in pediatric patients at early phase of disease.
In clinical practice, the laboratory parameters indicative of liver and renal damage were regularly used for auxiliary diagnosis of SFTS. As displayed in the current pediatric patients, laboratory parameters indicative of liver damage (AST, ALT, LDH, CK), instead of renal damage (BUN, CREA and ALB) was manifested. The evaluation of AST, ALT, LDH and CK could play roles in the auxiliary diagnosis; however they need to be used cautiously, as these evaluations might not be elevated at early infection and also kept at normal levels in certain pediatrics during the whole hospitalization.
Disease severity of patients infected with SFTSV varied, depending on multiple factors, including the virulence of different strains, access to the health system, the host factors, as well as other unknown reasons. Since the current pediatric patients acquired infection from the same region during the same period with adult patients, the impact from infected viral strain was supposed to be minor. Moreover, the children have better access to the health system. The comparably milder disease in pediatric patients therefore might be derived from the host factor. Jin et al. have demonstrated that virus replication and overexuberant immune responses can contribute to progressive organ damage . Moreover, dramatically elevated proinflammatory cytokine levels have been detected in severe or fatally infected patients, suggestive of a cytokine storm might contribute to the adverse disease outcome [10–12]. Children are physically different with adults and the incomplete maturation of the immune system could pose as one possible mechanism underlying their milder disease manifestation in comparison to adult patients . This mechanism had been applied in explaining the similarly milder clinical course of Crimean–Congo hemorrhagic fever (CCHF) in children than the adults .
The current study is subject to major limitation that only observation study was made on four patients without statistical analysis performed to draw validated conclusion. This needs to be addressed by study of large sample size in the future.
The research protocol was approved by the Human Ethics Committee of the 154 Hospital (No. 003/51). All guardians of the participants provided written informed consent.
Written informed consent was obtained from the patient for publication of this Case report and any accompanying images. A copy of the written consent is available for review by the Editor of this journal.
Severe fever with thrombocytopenia syndrome
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Yu XJ, Liang MF, Zhang SY, Liu Y, Li JD, Sun YL, Zhang LH, Zhang QF, Pobov VL, Li C, Qu J, Li Q, Zhang YP, Hai R, Wu W, Wang Q, Zhan FX, Wang XJ, Kan B, Wang SW, Wan KY, Jing HQ, Lu JX, Yin WW, Zhou H, Guan XH, Liu JF, Bi ZQ, Liu ZH, Ren J, et al: Fever with thrombocytopenia associated with a novel bunyavirus in China. N Engl J Med. 2011, 364 (16): 1523-1532. 10.1056/NEJMoa1010095.
Wu Y, Gao GF: Severe fever with thrombocytopenia syndrome virus expands its borders. Emerg Microb Infect. 2013, 2: e36-10.1038/emi.2013.36. doi:10.1038/emi.2013.36
Chang MS, Woo JH: Severe fever with Thrombocytopenia syndrome: tick-mediated viral disease. J Korean Med Sci. 2013, 28: 795-796. 10.3346/jkms.2013.28.6.795.
Denic S, Janbeih J, Nair S, Conca W, Tarig WU, Al-Aslam S: Acute thrombocytopenia, leucopenia, and multiorgan dysfunction: the first case of SFTS bunyavirus outside China?. Infect Dis. 2011, 12: doi:10.1155/2011/204056
McMullan LK, Folk SM, Kelly AJ, MacNeil A, Goldsmith CS, Metcalfe MG, Batten BC, Albarino CG, Zaki SR, Rollin PE, Nicholson WL, Nichol ST: A new phlebovirus associated with severe febrile illness in missouri. N Engl J Med. 2012, 367 (9): 834-841. 10.1056/NEJMoa1203378.
Gai Z, Liang M, Zhang Y, Zhang S, Jin C, Wang SW, Sun L, Zhou N, Zhang Q, Sun Y, Ding SJ, Li C, Gu W, Zhang F, Wang Y, Bian P, Li X, Wang Z, Song X, Wang X, Xu A, Bi Z, Chen S, Li D: Person-to-person transmission of severe fever With thrombocytopenia syndrome bunyavirus through blood contact. Clin Infect Dis. 2012, 54 (2): 249-252. 10.1093/cid/cir776.
Liu W, Lu QB, Cui N, Li H, Wang LY, Liu K, Yang ZD, Wang BJ, Wang HY, Zhang YY, Zhuang L, Hu CY, Yuan C, Fan XJ, Wang Z, Zhang L, Zhang XA, Walker DH, Cao WC: Case-fatality ratio and effectiveness of ribavirin therapy among hospitalized patients in china who had severe fever with thrombocytopenia syndrome. Clin Infect Dis. 2013, 57 (9): 1292-1299. 10.1093/cid/cit530.
Ministry of Health, China: Announcement of the Guidelines for Preventing and Controlling the Severe Fever with Thrombocytopenia Syndrome Disease. 2010, Availableat: http://www.moh.gov.cn/publicfiles/business/htmlfiles/wsb/pwsyw/ 201009/49245.htm,
Jin C, Liang M, Ning J, Gu W, Jiang H, Wu W, Zhang F, Li C, Zhang Q, Zhu H, Chen T, Han Y, Zhang W, Zhang S, Wang Q, Sun L, Liu Q, Li J, Wang T, Wei Q, Wang S, Deng Y, Qin C, Li D: Pathogenesis of emerging severe fever with thrombocytopenia syndrome virus in C57/BL6 mouse model. Proc Natl Acad Sci U S A. 2012, 109 (25): 10053-10058. 10.1073/pnas.1120246109.
Deng B, Zhang S, Geng Y, Zhang Y, Wang Y, Yao W, Wen Y, Cui W, Zhou Y, Gu Q, Wang W, Wang Y, Shao Z, Wang Y, Li C, Wang D, Zhao Y, Liu P: Cytokine and chemokine levels in patients with severe fever with thrombocytopenia syndrome virus. PLoS One. 2012, 7 (7): e41365-10.1371/journal.pone.0041365.
Zhang YZ, He YW, Dai YA, Xiong YW, Zheng Hm Zhou DJ, Li J, Sun QZ, Luo XL, Cheng YL, Tian JH, Chen XP, Yu B, Jin D, Guo WP, Li W, Wang W, Peng JS, Zhang GB, Zhang SM, Chen XM, Wang Y, Li MH, Li ZJ, Lu S, Ye CY, Jong MD, Xu JG: Hemorrhagic fever caused by a novel bunyavirus in China: pathogenesis and correlates of fatal outcome. Clin Infect Dis. 2012, 54 (4): 527-533. 10.1093/cid/cir804.
Sun Y, Jin C, Zhan FX, Wang XJ, Liang MF, Zhang QF, Ding SJ, Guan XH, Huo XX, Li C, Qu J, Wang Q, Zhang S, Zhang YP, Wang SW, Xu AQ, Bi ZQ, Li DX: Host cytokine storm is associated with disease severity of severe fever with thrombocytopenia syndrome. J Infect Dis. 2012, 206: 1085-1094. 10.1093/infdis/jis452.
Ozsurekci Y, Arasli M, Karadag Oncel E, Caglayik DY, Kaya A, Icagasioglu FD, Engin A, Korukluoglu G, Elaldi N, Ceyhan M: Can the mild clinical course of crimean-congo hemorrhagic fever in children be explained by cytokine responses?. J Med Virol. 2013, 85 (11): 1955-1959. 10.1002/jmv.23697.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/14/366/prepub
This study was supported by the China Mega-Project for Infectious Diseases grant (2013ZX10004-202), Natural Science Foundation of China (81222037, 81290344, 81130086), The funding agencies had no role in the design and conduct of the study, collection, management, analysis, interpretation of the data, preparation, review, or approval of the manuscript.
The authors declare that they have no competing interests.
WCC and WL conceptualized and designed the study and approved the final manuscript as submitted. LYW and YW carried out the experiments and drafted and reviewed the manuscript, and approved the final manuscript as submitted. NC, QBL and HYW collected the samples and information of the patients, analyzed the data and made the figures, reviewed and approved the manuscript.
Li-Yuan Wang, Ning Cui contributed equally to this work.
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Wang, L., Cui, N., Lu, Q. et al. Severe fever with thrombocytopenia syndrome in children: a case report. BMC Infect Dis 14, 366 (2014). https://doi.org/10.1186/1471-2334-14-366
- Severe fever with thrombocytopenia syndrome