Skip to main content

Coronavirus disease 2019 and dengue: two case reports



The pandemic of this century has overwhelmed the healthcare systems of affected countries, and all resources have been diverted to coronavirus disease 2019. At the onset, coronavirus disease 2019 can present as any other acute febrile undifferentiated illness. In tropical regions, clinicians are increasingly challenged to differentiate these febrile illnesses without the use of diagnostics. With this pandemic, many of these tropical diseases are neglected and go underreported. Dengue is holoendemic in the Maldives, and dengue viruses circulate throughout the year. Reports about coinfections with dengue virus and severe acute respiratory syndrome coronavirus 2 are scarce, and the outcome and the dynamics of the disease may be altered in the presence of coinfection. We have described the clinical manifestation and serial laboratory profile, and highlighted the atypical findings uncommon in dengue infection.

Case presentation

Case 1 was a 39-year old Asian male, presented on day 6 of dengue infection with warning signs. Reverse transcription polymerase chain reaction for severe acute respiratory syndrome coronavirus 2 that was done as per hospital protocol was found to be positive. Case 2 was a 38-year old Asian male, was admitted on day 5 of illness with symptoms of acute respiratory infection with positive reverse transcription polymerase chain reaction for severe acute respiratory syndrome coronavirus 2. Evaluation of progressive leukopenia and thrombocytopenia showed positive dengue serology.


Clinicians must be conscientious when working on the differential diagnosis of possible tropical diseases in cases of coronavirus disease 2019, specifically, when patients develop hemoconcentration, thrombocytopenia, and transaminitis with elevated expression of aspartate higher than alanine transaminase, which is frequently observed in dengue infection. Caution must be taken during the administration of intravenous fluids when treating patients with coronavirus disease 2019 and dengue coinfection, as coronavirus disease 2019 patients are more prone to develop pulmonary edema. Timely diagnosis and appropriate management are essential to avoid the devastating complications of severe forms of dengue infection. It is important to repeat and reconfirm the dengue serology in coronavirus disease 2019 patients to avoid false positivity. Diligence and care must be taken not to neglect other endemic tropical diseases in the region during the present pandemic.

Peer Review reports


The coronavirus disease 2019 (COVID-19) pandemic began in late December 2019. Over 19 million confirmed cases and 700,000 fatalities have been reported. At present, only 12 countries worldwide have not been affected by COVID-19 [1]. The first case of COVID-19 in the Maldives was confirmed on 7 March 2020 [2]. Most of the confirmed cases were asymptomatic, and among the symptomatic cases a majority had mild to moderate disease and a minority were critical. To date, the Maldives has had over 4769 confirmed cases of COVID-19 and 19 fatalities [3]. Several arboviral infections and other tropical diseases are endemic to the Maldives [4,5,6,7,8,9,10,11,12,13]. Among these, the most commonly diagnosed is dengue infection because of the widespread use of commercially available serological rapid diagnostic test kits [14]. Annually, the Maldives experiences a peak in the number of reported cases during the dengue outbreaks, especially during the monsoons. Factors contributing to this are poor vector control due to congested urbanization and limited efforts to segregate accumulated waste, which are potential vector breeding grounds [15]. As the COVID-19 pandemic has been the prime focus of attention in the past 7 months, many of the existing problems such as dengue have been neglected. Severe forms of dengue if left undetected can be fatal [16,17,18]. These include dengue hemorrhagic fever, where in addition to bleeding, plasma leakage occurs and expanded dengue syndrome with multisystemic involvement. These classifications are now collectively referred to as severe dengue [19]. Many countries where dengue is endemic have expressed concerns over the devastating impact a dengue outbreak could have during the COVID-19 pandemic [20,21,22], while others express how dengue and COVID-19 share similarities in both clinical and laboratory findings [23]. One report demonstrated a false dengue serological test in a COVID-19 case [24]. There are also reports of serological overlap resulting in false positive dengue serology [25]. Reports about coinfections with dengue virus and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are scarce [24, 26]. Herein, we describe the clinical manifestation and serial laboratory profile and highlight the atypical findings uncommon in dengue fever and dengue hemorrhagic fever when coinfected with SARS-CoV-2.

Case presentation

Case 1

A 39-year-old, Asian male, who is a migrant worker presented to the emergency department with a history of persistent high-grade fever, retro-orbital headache, fatigue, and myalgia for the past 6 days. He also complained of right upper quadrant pain, vomiting, and loose stools. There was no history of rash, arthralgia, or bleeding. On physical examination, he was dehydrated and the vitals recorded were a body temperature of 37.5°C, heart rate of 80 beats per minute, blood pressure of 113/78 mmHg, pulse pressure of 35 mmHg, respiratory rate of 20 breaths per minute, capillary refill time of less than 2 seconds, and oxygen saturation of 98% in room air. Systemic examination was unremarkable except for right upper quadrant tenderness with a normal liver span. Bedside ultrasonography of the abdomen revealed gall bladder wall edema. The laboratory investigations at presentation and serial laboratory profiles are tabulated in Table 1, which shows hemoconcentration of 19% and transaminitis. Dengue rapid test (SD BIOLINE Dengue DUO®) revealed a negative non-structural protein 1 (NS1) with a positive immunoglobulin (Ig)M and IgG. This was later reconfirmed with a positive dengue enzyme-linked immunosorbent assay (ELISA) IgM and IgG (Panbio® Standard Diagnostics). Reverse transcription polymerase chain reaction (rRT-PCR) (LiferiverTM 2019-nCoV Real Time Multiplex RT-PCR Kit) for COVID-19 done as per hospital admission protocol was positive with a cycle threshold of 28.35. The patient was admitted to a COVID-19 facility and kept in isolation with a diagnosis of dengue hemorrhagic fever grade I with COVID-19. As the patient was vitally stable with a minimal increase in hemoconcentration, he was managed conservatively with oral fluids. On day 5 of illness, the patient developed non-productive cough and sore throat for which a chest X-ray was done and no abnormality was found. The patient was monitored daily to look for development of warning signs of dengue fever, including hemoconcentration. The patient had an uneventful hospital stay and was discharged after completing the mandatory isolation period of 14 days.

Table 1 Serial laboratory parameters during the course of illness, Case 1

Case 2

A 38-year-old Asian male presented with a history of intermittent fever and generalized headache for the past 5 days. He also complained of sore throat, dysgeusia, and anosmia for a duration of 3 days following the onset of fever. Being a close contact of a COVID-19 patient, he consulted an online clinic where he was referred to the hospital for evaluation. On examination, he appeared dehydrated, with a body temperature of 37.4°C, pulse rate of 84 beats per minute, blood pressure of 100/60 mmHg, pulse pressure of 40 mmHg, respiratory rate of 21 breaths per minute, capillary refill time of less than 2 seconds, and oxygen saturation of 97% in room air. Other systemic examination was unremarkable. With a positive rRT-PCR for SARS-CoV-2 (Ct value 24.45) he was admitted and kept in isolation. His laboratory parameters are tabulated in Table 2, which shows leukopenia and thrombocytopenia. In view of the depleting trend of total leukocyte count and platelets, a dengue rapid test was requested, which showed a negative NS1 and positive IgM/IgG. This was reconfirmed with a positive dengue ELISA serology of anti-dengue IgM and IgG. Hence, the patient was diagnosed with COVID-19 with dengue fever. The patient had minimal hemoconcentration, and as he was able to take fluids adequately he was managed with oral fluids and monitored daily for the development of warning signs of dengue or worsening of the severity of COVID-19. The patient did not have any fever spikes after admission. The patient’s platelets gradually improved, and symptoms resolved over a period of 1 week. The patient was discharged after completing the 14-day mandatory period of isolation.

Table 2 Serial laboratory parameters during the course of illness, Case 2


Here we describe two cases of coinfection of dengue fever and COVID-19. The first case had presented with symptoms of dengue fever, and after 5 days of admission he developed symptoms of COVID-19. The second case was admitted with mild COVID-19, and during the course of illness, in view of mild hemoconcentration and progressive decline in leukocyte and thrombocyte counts, he was tested positive for dengue fever. In coinfections, one virus can suppress or augment the other, leading to varying clinical manifestations of the diseases.

The COVID-19 pandemic has spread across the globe, including areas where other tropical diseases are endemic such as the Maldives [6, 8,9,10, 15]. Clinicians are challenged with the additional burden of possible coinfections with other tropical diseases that have the potential to complicate the course of illness [26]. Coinfections with COVID-19 have been reported with multiple bacteria and viruses [27,28,29,30,31]. Nevertheless, coinfection with dengue viruses and SARS-CoV-2 are still scarce, with only a few reports describing false-positive dengue serology [24, 32]. The healthcare system of the Maldives is stretched and may not respond adequately to a dual outbreak because of limited manpower and infrastructure [33]. Every year, the Maldives experiences a dengue outbreak during the monsoons. From the year 2011, an average of 1543 cases have been reported annually [15]. In 2018, 3494 cases were reported, and in 2019, 5023 cases were reported, which was a record number for the Maldives [34]. Despite an expected increase in cases, so far only 225 cases have been reported, while dengue cases are on the rise in other endemic regions [34, 35]. We postulate that healthcare providers are more focused on COVID-19, which has resulted in lower rates of testing or reporting of dengue virus. In addition, individuals with mild symptomatic dengue infections perhaps are not visiting hospitals because of the pandemic and lockdowns. COVID-19 may present as an undifferentiated acute febrile illness [36]. In one study, 87.9% of COVID-19 patients presented with fever, 67.7% presented with cough, and 13.7% of patients had headache [37]. Nevertheless, information regarding the frequency of fever in dengue infection is limited in most prospective studies, mostly due to confounders within the study designs where fever remains an inclusion criterion. Fever can be absent in the elderly population or, if present, can occur over 90% of the time [38]. Cough in dengue infection has been reported in 67% of cases, which can be due to pleural effusion observed during plasma leakage in dengue hemorrhagic fever (DHF) [39, 40]. Headache in dengue infection has been reported in 89% of cases and more commonly in DHF [41]. Bleeding in COVID-19 has been reported to be associated with morbidity, but frequency of bleeding manifestations in COVID-19 remains low [42]. In contrast, bleeding in dengue infection occurs more frequently and is associated with increasing severity [41]. The hematological profile in COVID-19 and dengue infection are similar. Neutrophils are increased early in both infections with leukopenia and thrombocytopenia. The discrepancy in the hematological profile in both infections is lymphopenia, which is observed in COVID-19 during the course of illness in contrast to a reverse neutrophil-to-lymphocyte ratio in dengue infection. Transaminitis is observed in both infections; however, the expression of aspartate aminotransferase is greater than alanine transaminase in dengue infection [43, 44]. Our first case was initially diagnosed as dengue fever with warning signs, and COVID-19 was detected during the screening process before admission [45]. On day 5 of admission, he developed a non-productive cough and sore throat that could be attributed to COVID-19. The cough could also be due to dengue-related pleural effusion, which was not evident on his chest X-ray in posterior–anterior view. However, a chest X-ray in lateral decubitus view is more sensitive to detect minimal effusion [46]. In our second case, the patient was admitted with a diagnosis of mild COVID-19. With a depleting trend of leukocytes and platelets, dengue serology was performed, which was positive. Case 1 had a hemoconcentration of 19% and gall bladder wall edema suggestive of plasma leakage [47]. As there was no bleeding manifestation, this case was classified as DHF grade 1 [48]. In case 1, liver biochemistry revealed an atypical profile with alanine transaminase expression greater than that of aspartate aminotransferase, which may be due to coinfection. However, initially in case 2, we observed mild transaminitis with an elevation of aspartate aminotransferase expression compared with that of alanine transaminase, which is consistent with dengue infection. Case 2 had leukopenia, which may be seen in both infections, which started to improve on day 3 of admission. In both cases, NS1 was negative, which could have been due to the late presentation. Treatment was mainly symptomatic. Intravenous fluid was avoided as COVID-19 patients are more prone to develop pulmonary edema [49]. Coinfections of two viruses can reduce or augment disease severity [50]. The most common outcome is viral interference, where one virus competitively suppresses the replication of the other [51]. This could have played an important role in changing the dynamics of dengue virus infection and the natural history of the disease. This could explain the two cases failing to demonstrate the typical features of dengue infection, both in its disease progression and the laboratory findings. More data are required to determine the changing dynamics of coinfection of the dengue virus with SARS-CoV-2. Furthermore, clinicians should use commercially available dengue serology judiciously with growing evidence of cross-reaction with other flaviviruses [52]. Limitations in this report include the inability to utilize the gold standard to diagnose dengue infection either by virus isolation or RT-PCR. In addition to this, dengue serotyping was also not done, which could have provided valuable information regarding virulence and disease dynamics.


During this pandemic, it is important to consider other tropical diseases that are endemic to the tropics, such as dengue, Zika, chikungunya infections, or scrub typhus. Coinfection with two viruses may change the dynamics and natural history of disease progression, which may result in atypical presentation of dengue infection and COVID-19. In cases of COVID-19 with atypical presentations, such as increased hematocrit, depleted platelets, and transaminitis with a greater expression of aspartate aminotransferase than of alanine transaminase, dengue infection should be considered. In COVID-19 patients with positive dengue serology, it is important to repeat and reconfirm the test to avoid false positivity. It is important to keep an open mind when treating patients with COVID-19 and be vigilant of atypical signs and symptoms that may indicate any other tropical infection. Clinicians should be cautious in giving intravenous fluids when treating patients with COVID-19 and dengue coinfection, as COVID-19 patients are more prone to develop pulmonary edema.

Availability of data and materials

Not applicable.


  1. 1.

    University JH. COVID-19 Dashboard by the Center for Systems Science and Engineering (CSSE) at Johns Hopkins University (JHU)

  2. 2.

    Health Mo. First cases of COVID-19 confirmed in the Maldives. 2020.

  3. 3.

    Agency HP. COVID-19 Statistics Dashboard.

  4. 4.

    Trojanek M, Tomickova D, Rohacova H, Kosina P, Gebousky J, Dvorak J, et al. Dengue fever cases in Czech workers returning from the Maldives. Epidemiol Mikrobiol Imunol. 2013;62:100–5.

    PubMed  Google Scholar 

  5. 5.

    Mutoh Y, Moriya A, Yasui Y, Saito N, Takasaki T, Hiramatsu S, et al. Two cases of dengue virus type 2 (DENV-2) infection in a Japanese couple returning from the Maldives during the 2018 dengue outbreak. Jpn J Infect Dis. 2020;73:58–60.

    Article  Google Scholar 

  6. 6.

    Korhonen EM, Huhtamo E, Smura T, Kallio-Kokko H, Raassina M, Vapalahti O. Zika virus infection in a traveller returning from the Maldives, June 2015. Euro Surveill. 2016;21:99.

    Article  Google Scholar 

  7. 7.

    Yoosuf AA, Shiham I, Mohamed AJ, Ali G, Luna JM, Pandav R, et al. First report of chikungunya from the Maldives. Trans R Soc Trop Med Hyg. 2009;103:192–6.

    Article  Google Scholar 

  8. 8.

    Dudouet P, Gautret P, Larsen CS, Diaz-Menendez M, Trigo E, von Sonnenburg F, et al. Chikungunya resurgence in the Maldives and risk for importation via tourists to Europe in 2019–2020: a GeoSentinel case series. Travel Med Infect Dis. 2020;9:101814.

    Article  Google Scholar 

  9. 9.

    Imad HA, Riza S, Reesha F, Ali A, Muaz M, Sujau I, et al. Severe typhoid in Maldives. 11th International Conference on Typhoid and other Invasive Salmonelloses. 2019.

  10. 10.

    Imad HA, Tanyaratsrisakul S, Piyaphanee W, Wattanagoon Y. Skin lesion from Maldives: classic but forgotten. Travel Med Infect Dis. 2017;17:74–5.

    Article  Google Scholar 

  11. 11.

    Receveur M, Ezzedine K, Pistone T, Malvy D. Chikungunya infection in a French traveller returning from the Maldives, October 2009. Euro Surveill. 2010;15:19494.

    CAS  Article  Google Scholar 

  12. 12.

    Pfeffer M, Hanus I, Loscher T, Homeier T, Dobler G. Chikungunya fever in two German tourists returning from the Maldives, September 2009. Euro Surveill. 2010;15:9.

    Google Scholar 

  13. 13.

    Lewis MD, Yousuf AA, Lerdthusnee K, Razee A, Chandranoi K, Jones JW. Scrub typhus reemergence in the Maldives. Emerg Infect Dis. 2003;9:1638–41.

    Article  Google Scholar 

  14. 14.

    Abdulla AA, Rasheeda F, Ahmed IN, Aboobakur M. An evaluation of the surveillance system for dengue virus infections in Maldives. WHO South East Asia J Public Health. 2014;3:60–8.

    Article  Google Scholar 

  15. 15.

    Bangert M, Latheef AT, Dev Pant S, Nishan Ahmed I, Saleem S, Nazla Rafeeq F, et al. Economic analysis of dengue prevention and case management in the Maldives. PLoS Negl Trop Dis. 2018;12:e0006796.

    Article  Google Scholar 

  16. 16.

    Laoprasopwattana K, Chaimongkol W, Pruekprasert P, Geater A. Acute respiratory failure and active bleeding are the important fatality predictive factors for severe dengue viral infection. PLoS ONE. 2014;9:e114499.

    Article  Google Scholar 

  17. 17.

    Wei HY, Shu PY, Hung MN. Characteristics and risk factors for fatality in patients with dengue hemorrhagic fever, Taiwan, 2014. Am J Trop Med Hyg. 2016;95:322–7.

    CAS  Article  Google Scholar 

  18. 18.

    Magpusao NS, Monteclar A, Deen JL. Slow improvement of clinically-diagnosed dengue haemorrhagic fever case fatality rates. Trop Doct. 2003;33:156–9.

    Article  Google Scholar 

  19. 19.

    Wiwanitkit V. Accuracy and applicability of the revised WHO classification (2009) of dengue. Infection. 2013;41:1047.

    CAS  Article  Google Scholar 

  20. 20.

    Wu D, Lu J, Liu Q, Ma X, He W. To alert coinfection of COVID-19 and dengue virus in developing countries in the dengue-endemic area. Infect Control Hosp Epidemiol. 2020;22:1.

    Article  Google Scholar 

  21. 21.

    Saavedra-Velasco M, Chiara-Chilet C, Pichardo-Rodriguez R, Grandez-Urbina A. Inga-Berrospi F [Coinfection between dengue and covid-19: need for approach in endemic zones.]. Rev Fac Cien Med Univ Nac Cordoba. 2020;77:52–4.

    Article  Google Scholar 

  22. 22.

    Miah MA, Husna A. Coinfection, coepidemics of COVID-19, and dengue in dengue-endemic countries: a serious health concern. J Med Virol. 2020;8:22.

    Google Scholar 

  23. 23.

    Henrina H, Putra I, Lawrensia S, Handoyono Q, Alius C. Coronavirus disease of 2019: a mimicker of dengue infection? SN Comprehensive Clinical Medicine 2020.

  24. 24.

    Yan G, Lee CK, Lam LTM, Yan B, Chua YX, Lim AYN, et al. Covert COVID-19 and false-positive dengue serology in Singapore. Lancet Infect Dis. 2020;20:536.

    CAS  Article  Google Scholar 

  25. 25.

    Kembuan GJ. Dengue serology in Indonesian COVID-19 patients: coinfection or serological overlap? IDCases. 2020;22:e00927.

    Article  Google Scholar 

  26. 26.

    Tun SZ. Thailand records first coronavirus death: health official. REUTERS. 2020.

  27. 27.

    Toombs JM, Van den Abbeele K, Democratis J, Mandal AKJ, Missouris CG. Pneumococcal coinfection in COVID-19 patients. J Med Virol. 2020.

  28. 28.

    Ozaras R, Cirpin R, Duran A, Duman H, Arslan O, Bakcan Y, et al. Influenza and COVID-19 coinfection: report of six cases and review of the literature. J Med Virol. 2020.

  29. 29.

    Menon AA, Berg DD, Brea EJ, Deutsch AJ, Kidia KK, Thurber EG, et al. A case of COVID-19 and Pneumocystis jirovecii coinfection. Am J Respir Crit Care Med. 2020;202:136–8.

    CAS  Article  Google Scholar 

  30. 30.

    Khaddour K, Sikora A, Tahir N, Nepomuceno D, Huang T. Case report: the importance of novel coronavirus disease (COVID-19) and coinfection with other respiratory pathogens in the current pandemic. Am J Trop Med Hyg. 2020;102:1208–9.

    Article  Google Scholar 

  31. 31.

    Fan BE, Lim KGE, Chong VCL, Chan SSW, Ong KH, Kuperan P. COVID-19 and Mycoplasma pneumoniae coinfection. Am J Hematol. 2020;95:723–4.

    CAS  Article  Google Scholar 

  32. 32.

    Joob B, Wiwanitkit V. COVID-19 can present with a rash and be mistaken for dengue. J Am Acad Dermatol. 2020;82:e177.

    CAS  Article  Google Scholar 

  33. 33.

    Maldives U. Addressing the socio-economic impact of COVID-19 on the Maldives 2020.

  34. 34.

    Health Mo. Monthly Communicable Disease Report. 2020.

  35. 35.

    Control ECfDPa. Dengue worldwide overview. 2020.

  36. 36.

    Nunthavichitra S, Prapaso S, Luvira V, Muangnoicharoen S, Leaungwutiwong P, Piyaphanee W. Case report: COVID-19 presenting as acute undifferentiated febrile illness—a tropical world threat. Am J Trop Med Hyg. 2020;103:83–5.

    Article  Google Scholar 

  37. 37.

    Guan WJ, Ni ZY, Hu Y, Liang WH, Ou CQ, He JX, et al. Clinical characteristics of coronavirus disease 2019 in China. N Engl J Med. 2020;382:1708–20.

    CAS  Article  Google Scholar 

  38. 38.

    Rowe EK, Leo YS, Wong JG, Thein TL, Gan VC, Lee LK, et al. Challenges in dengue fever in the elderly: atypical presentation and risk of severe dengue and hospital-acquired infection [corrected]. PLoS Negl Trop Dis. 2014;8:e2777.

    Article  Google Scholar 

  39. 39.

    Restrepo BN, Beatty ME, Goez Y, Ramirez RE, Letson GW, Diaz FJ, et al. Frequency and clinical manifestations of dengue in urban Medellin. Colombia J Trop Med. 2014;2014:872608.

    PubMed  Google Scholar 

  40. 40.

    Marchiori E, Hochhegger B, Zanetti G. Pulmonary manifestations of dengue. J Bras Pneumol. 2020;46:e20190246.

    Article  Google Scholar 

  41. 41.

    Imad HA, Phumratanaprapin W, Phonrat B, Chotivanich K, Charunwatthana P, Muangnoicharoen S, et al. Cytokine expression in dengue fever and dengue hemorrhagic fever patients with bleeding and severe hepatitis. Am J Trop Med Hyg. 2020;102:943–50.

    Article  Google Scholar 

  42. 42.

    Al-Samkari H, Karp Leaf RS, Dzik WH, Carlson JCT, Fogerty AE, Waheed A, et al. COVID-19 and coagulation: bleeding and thrombotic manifestations of SARS-CoV-2 infection. Blood. 2020;136:489–500.

    CAS  Article  Google Scholar 

  43. 43.

    Samanta J, Sharma V. Dengue and its effects on liver. World J Clin Cases. 2015;3:125–31.

    Article  Google Scholar 

  44. 44.

    Ong J, Young BE, Ong S. COVID-19 in gastroenterology: a clinical perspective. Gut. 2020;69:1144–5.

    CAS  Article  Google Scholar 

  45. 45.

    Organization WH. Handbook for clinical management of dengue, WHO and Special Programme for Research and Training in Tropical Diseases (TDR) report. 2012.

  46. 46.

    Kalayanarooj S. Clinical manifestations and management of dengue/DHF/DSS. Trop Med Health. 2011;39:83–7.

    Article  Google Scholar 

  47. 47.

    Tavares MA, Joao GAP, Bastos MS, Gimaque JBL, Almeida ACG, Ngo TT, et al. Clinical relevance of gallbladder wall thickening for dengue severity: a cross-sectional study. PLoS ONE. 2019;14:e0218939.

    CAS  Article  Google Scholar 

  48. 48.

    Hadinegoro SR. The revised WHO dengue case classification: does the system need to be modified? Paediatr Int Child Health. 2012;32(Suppl 1):33–8.

    Article  Google Scholar 

  49. 49.

    Dagens A, Sigfrid L, Cai E, Lipworth S, Cheng V, Harris E, et al. Scope, quality, and inclusivity of clinical guidelines produced early in the covid-19 pandemic: rapid review. BMJ. 2020;369:m1936.

    Article  Google Scholar 

  50. 50.

    Diaz-Munoz SL. Viral coinfection is shaped by host ecology and virus-virus interactions across diverse microbial taxa and environments. Virus Evol. 2017;3:vex011.

    Article  Google Scholar 

  51. 51.

    Kumar N, Sharma S, Barua S, Tripathi BN, Rouse BT. Virological and immunological outcomes of coinfections. Clin Microbiol Rev. 2018;31:23.

    Article  Google Scholar 

  52. 52.

    Suzuki K, Nakayama EE, Saito A, Egawa A, Sato T, Phadungsombat J, et al. Evaluation of novel rapid detection kits for dengue virus NS1 antigen in Dhaka, Bangladesh, in 2017. Virol J. 2019;16:102.

    Article  Google Scholar 

Download references


We would like to express our sincere appreciation to all the front-liners across the globe for their bravery and dedication in combating this unprecedented event in our present lifetime. In addition, we would like to thank all the staff working at Indira Gandhi Memorial Hospital and the COVID-19 facility, including everyone at the multiagency taskforce overseeing the management of the current pandemic in the Maldives.


There was no financial support for this clinical case report.

Author information




AIH: conceptualization, writing original draft, data collection; RKD: writing review and editing, data collection; HAI: writing review and editing; AN: review and validation; AAY: review and validation; AAL: supervision, review and validation. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Abdullah Isneen Hilmy.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Written informed consent was obtained from the patients for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Hilmy, A.I., Dey, R.K., Imad, H.A. et al. Coronavirus disease 2019 and dengue: two case reports. J Med Case Reports 15, 171 (2021).

Download citation


  • COVID-19
  • Dengue
  • Coinfection
  • Pandemic
  • Case report