Atypical hepatic, cardiac, and renal manifestations in pediatric dengue: a prospective study

Authors

  • Dhanush Kumar N. Department of Paediatrics, Navodaya Medical College, Hospital and Research Centre, Raichur, Karnataka, India
  • Kasula Shravani Department of Paediatrics, Navodaya Medical College, Hospital and Research Centre, Raichur, Karnataka, India
  • Sanjeev Chetty Department of Paediatrics, Navodaya Medical College, Hospital and Research Centre, Raichur, Karnataka, India

DOI:

https://doi.org/10.18203/2349-3291.ijcp20261907

Keywords:

Dengue, Expanded dengue syndrome, Hepatic dysfunction, Pediatric dengue, Acute kidney injury, Myocarditis

Abstract

Background: Dengue fever is the most prevalent arboviral infection worldwide and is characterized by a broad clinical spectrum, ranging from self-limiting febrile illness to severe, life-threatening complications. In recent years, there has been growing recognition of atypical presentations, collectively referred to as expanded dengue syndrome (EDS), encompassing involvement of organs such as the liver, heart, and kidneys. The aim of this study was to evaluate the atypical hepatic, cardiac, and renal manifestations in children with dengue infection.

Methods: This prospective cohort study included 100 pediatric patients with serologically confirmed dengue infection. All participants underwent detailed clinical assessment along with laboratory investigations, including complete blood counts (CBC), liver function tests (LFT), renal function tests (RFT), coagulation profiles, and electrocardiographic (ECG)evaluation.

Results: The mean age of the study population was 8.65±3.34 years, with a slight male predominance (55%). Serological analysis showed that 72% of patients were positive for NS1 antigen alone, whereas 28% demonstrated both NS1 and IgM positivity. Hepatic involvement was common, with elevated SGOT levels observed in 51% of cases, while SGPT elevation was noted in only 6%. Hematological abnormalities were prominent, with anemia detected in 93% and thrombocytopenia in 86% of patients. Renal involvement was relatively infrequent; elevated serum creatinine was seen in 9% of cases, and proteinuria in 1%. No electrocardiographic abnormalities were identified in the study cohort. On subgroup analysis, patients with combined NS1 and IgM positivity had significantly lower platelet counts (p=0.0397) and hemoglobin levels (p<0.0001) compared to those with isolated NS1 positivity.

Conclusions: Hepatic transaminitis and hematological cytopenias constitute common systemic manifestations, with occasional atypical involvement in pediatric dengue. Concurrent positivity for NS1 antigen and IgM antibody is associated with a more severe clinical profile, suggesting its potential role as a marker of disease severity.

References

World Health Organization. Dengue and severe dengue. Geneva: WHO; 2023. Available at: https://www.who.int/news-room/fact-sheets/detail/dengue-and-severe-dengue. Accessed on 12 March 2026.

World Health Organization. Handbook for clinical management of dengue. Geneva: World Health Organization; 2012.

Whitehorn J, Farrar J. Dengue. Br Med Bull. 2010;95:161-73.

Bhatt S, Gething PW, Brady OJ, Jane PM, Andrew WF, Catherine LM, et al. The global distribution and burden of dengue. Nature. 2013;496(7446):504-7.

Gupta N, Srivastava S, Jain A, Chaturvedi UC. Dengue in India. Indian J Med Res. 2012;136(3):373-90.

Guzman MG, Halstead SB, Artsob H, Philippe B, Jeremy F, Duane JG, et al. Dengue: a continuing global threat. Nat Rev Microbiol. 2010;8(12):S7-16.

Martina BE, Koraka P, Osterhaus AD. Dengue virus pathogenesis. Clin Microbiol Rev. 2009;22(4):564-81.

Diamond MS, Pierson TC. Molecular insight into dengue virus pathogenesis. Cell. 2015;162:488-92.

Kliegman RM, St Geme JW, Blum NJ, Shah SS, Tasker RC, Wilson KM. Nelson Textbook of Pediatrics. 22nd ed. Philadelphia: Elsevier. 2025.

Shu PY, Huang JH. Current advances in dengue diagnosis. Clin Diagn Lab Immunol. 2004;11(4):642-50.

Samanta J, Sharma V. Dengue and its effects on liver. World J Clin Cases. 2015;3(2):125-131.

Seneviratne SL, Malavige GN, de Silva HJ. Liver involvement in dengue infection. Trans R Soc Trop Med Hyg. 2006;100(7):608-14.

Dissanayake HA, Seneviratne SL. Liver involvement in dengue viral infections. Rev Med Virol. 2018;28(2):e1971.

Souza LJ, Alves JG, Nogueira RM, Carlos GN, Diogo AB, Edno WSS, et al. Aminotransferase changes in dengue. Braz J Infect Dis. 2004;8(2):156-63.

Kuo CH, Tai DI, Chang-Chien CS, Lan CK, Chiou SS, Liaw YF. Liver biochemical tests and dengue. Am J Trop Med Hyg. 1992;47(3):265-70.

Jagadishkumar K, Jain P, Manjunath VG, Umesh L. Hepatic involvement in dengue fever in children. Iran J Pediatr. 2012;22:231-6.

Lee LK, Gan VC, Lee VJ, Adriana ST, Yee SL, David CL. Liver enzyme elevation and dengue severity. PLoS Negl Trop Dis. 2012;6(1):e1676.

Poovorawan Y, Hutagalung Y, Chongsrisawat V, Irving B, Hans LB. Acute hepatic failure in dengue. Ann Trop Paediatr. 2006;26(1):17-23.

Promphan W, Sopontammarak S, Pruekprasert P, Wanchai K, Apichai K. Dengue myocarditis. Southeast Asian J Trop Med Public Health. 2004;35(3):611-3.

Nagaratnam N, Sripala K, De Silva N. Dengue myocarditis and pericarditis. Br Heart J. 1973;35:204-6.

Hommel D, Talarmin A, Reynes JM, Hulin A. Acute renal failure in dengue. Nephron. 1999;83(2):183.

Boonpucknavig V, Bhamarapravati N, Futrakul P, Tanpaichitr P. Renal pathology in dengue. Arch Pathol Lab Med. 1976;100(4):206-12.

Wiwanitkit V. Renal failure in dengue hemorrhagic fever. Ren Fail. 2005;27(5):647-8.

Pothapregada S, Kamalakannan B, Thulasingam M. Atypical manifestations of dengue. Indian J Pediatr. 2016;83(6):493-9.

Nimmagadda SS, Mahabala C, Boloor A, Pavan MR, Akshatha N. Atypical manifestations of dengue fever. J Clin Diagn Res. 2014;8(1):71-3.

Downloads

Published

2026-06-22

How to Cite

N., D. K., Shravani, K., & Chetty, S. (2026). Atypical hepatic, cardiac, and renal manifestations in pediatric dengue: a prospective study. International Journal of Contemporary Pediatrics, 13(7), 1159–1163. https://doi.org/10.18203/2349-3291.ijcp20261907

Issue

Section

Original Research Articles