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Dengue Hemorrhagic Fever and Acute Hepatitis: A Case Report


Arifa Akram
National Institute of Laboratory Medicine and Referral Center, Dhaka, Bangladesh.

Rasheduzzaman M
Dhaka Medical College and Hospital, Dhaka, Bangladesh.

Keywords: Dengue Hemorrhagic, asymptomatic, haemorrhagic, Hepatitis

DOI: 10.3329/bmrcb.v46i3.52260

Introduction

Bangladesh has achieved a remarkable progress in controlling communicable diseases, but still facing pressure in public health problems especially controlling the emerging or re-emerging diseases. Increase in dengue cases introduce threats to public health. Most of the cases of dengue virus infection remain asymptomatic; but it can cause a wide spectrum of clinical manifestations from mild illness to spontaneous recovery and also haemorrhagic dengue fever (DF) and/or dengue shock syndrome (DSS).1,2 There are four serotypes of dengue virus (DEN1-4) with 25-40% heterogeneity.3 Infection with one serotype confers lifelong immunity against that particular serotype but subsequent infection by another serotype often creates fatal outcomes if remains untreated.1

Since 1970, liver injury due to dengue infection has been described and it’s not uncommon. Dengue hemorrhagic fever (DHF) is associated with hepatomegaly in 30% of patients, and its magnitude has no relationship with the severity of the disease. On the other hand, 90% of people with dengue infection presented with an increase in aminotransferases, with levels of aspartate aminotransferase (AST) higher than those of alanine aminotransferase (ALT). Acute liver failure is a severe complicating factor in dengue infection, predisposing to life-threatening hemorrhage, disseminated intravascular coagulation and encephalopathy.4

The Case

A 28-year-old woman was admitted in Dhaka Medical College Hospital in April 2019. She was from Dhaka. Written informed consent was obtained from patient. She had a history of dengue fever three years earlier. She was 6 weeks pregnant at that time. Five days before admission, she developed fever, headache, chills, myalgia and arthralgia. She tested Dengue NS1 with the advice of family physician and it was positive. She took acetaminophen at standard dosages according to the instruction of that physician. On the fourth day of her symptoms, after a decrease in fever and headache, she had cold clammy skin, abdominal pain, repeated vomiting, per vaginal (PV) bleeding and diarrhoea. So, she was admitted in hospital on 5th day of her illness. On evaluation in the emergency department, she was well-nourished but icteric. Vital signs revealed pulse 100/min and BP 90/60 mm of Hg. A few petechial lesions were observed on the upper extremities and mildly painful liver enlargement was evident. The tourniquet test was not performed due to bleeding manifestations. The patient was hospitalized and submitted to a management protocol for DHF cases. She was given oral fluids and also intravenous saline solution. The results of laboratory tests were done. Tests of IgM HAV, HBsAg, anti HCV, and IgM HEV were also negative (table I). Ultrasound exam of her abdomen showed hepatomegaly with gall bladder wall thickening, minimal ascites and retained products of conception.

During the first 24 hours of hospitalization the patient had moderate PV bleeding, right upper abdominal pain, vomiting and unstable BP. She was managed conservatively with continuous IV fluids and daily vital monitoring. On the 7th day, her platelet count became 65000/µL, on 8th day it increased to 60000/µL, and on the 9th day it reached 1.3 lakhs/µL. Both IgM and IgG antibodies against dengue were strongly positive at day 6. One unit of packed cell was transfused on day 7. Her PV bleeding decreased from day 8. So, repeat ultrasound was done to see the condition of retained products. As there were no products, no D&C was performed. Jaundice slowly disappeared from day 9 and she was discharged on the 13th day. Her LFT and ultrasound of whole abdomen were normal at the time of discharge.

Investigations Day 5 Day 7 Day 8 Day 9 Day 13
Leukocytes (4000-11,000/cmm) 9400   20800   11000
Neutrophils (%) 66   55   45
Lymphocytes (adult 20-50%) 25   41   38
RBC (x 106/µL) 4.3        
Hemoglobin (g/dL) 10   9   10
Hematocrit (%) 42 46 40 32 31
Platelet (x 103/µL)   65000 60000 130000 160000
PT   13 sec 15 sec   12 sec
Albumin (g/dL)     2.7 2.5 3.4
AST U/L (<34) 7380   4765 2500 310
ALT U/L (<40) 2185   1280 500 220
ALP U/L (100-360) 499   360 280 80
LDH U/L (140-280) 5000   2020 800 300
Total bilirubin (0.1 -1.2 mg/dL) 4   2.5 1.5 0.7
S Ceatinine (mg/dL)     1.4   1.1

Discussion

Dengue virus infection can be presented with a diverse clinical spectrum. In Indonesia in 1970s, acute liver failure was initially reported in association with DHF/DSS. After that, it was reported during the 1987 epidemic in Thailand and the 1990 epidemic in Malaysia.5 Dengue virus serotypes 1, 2 and 3 have been isolated from the patients dying from liver failure with both primary and secondary dengue infection.6 Another study reported that DENV-3 and DENV-4 are related with a greater degree of hepatic involvement. Furthermore, there is a suggested correlation between acetaminophen administration for fever, and the degree of liver damage.7

The mechanism of liver failure is not fully cleared yet. It may be combined interactions of the virus, the host and the duration of disease. Replication phase in hepatocytes which causes hepatic injury, stimulating apoptosis, micro vesicular steatosis and the development of Councilman-Rocha Lima bodies, may contribute to disease aggravation.8 The histopathological observation of liver specimens is restricted to fatal cases because of the risk of bleeding diathesis in acutely ill patients.6

The liver involvement due to dengue infection in Thailand and Malaysia was reported as mild from 1973 to 1982, and it manifested exclusively as elevated liver enzymes. But, several cases of fulminant hepatitis with high mortality rate have been reported after this period, mainly in children and young adults.9 The increase in aminotransferases, mainly AST, has been associated with disease severity and may serve as an early indicator of dengue infection. Certainly, liver injury is a good positive predictive factor for the development of DHF.10 This increase usually happens within the first nine days of symptoms and normalizes in about two weeks. Increased levels of alkaline phosphatase and serum bilirubin are noted in some cases.7

In this case, patient had fever and was diagnosed as dengue (NS1 positive) with 6 weeks pregnancy and was on home management. But on the 5th day, when she developed abdominal pain, repeated vomiting, PV bleeding and diarrhea, she was admitted in hospital. She was hemodynamically unstable at that time. The appearance of jaundice with thrombocytopenia along with PV bleeding, all features made the condition of the patient unstable. The elevation in the AST level is usually greater than that of ALT in dengue infection, which is uncommon in patients with viral hepatitis A, B, or C.11 This patient also had greater elevation of AST compared to ALT elevation. Dengue fever should be considered when liver functions are deranged, because they are potential candidates for acute fulminant hepatic failure apart from routine hepatotropic viruses.10

The hypoalbuminaemia found in this case was probably a result of both capillary leakages induced by dengue infection and liver failure. Leukocytosis may be the cause of extensive acute hepatocyte necrosis.12

Conclusion

A high suspicion of dengue should be present when clinical and laboratory criteria are present in addition to that of jaundice. Countries that are endemic to dengue that have possible epidemic outbreaks should be kept in mind the different presentations which may mask dengue fever.

References

  1. Shirin T. Dengue Fever in Bangladesh. Bangladesh Medical Research Council Bulletin. 2019: 45:214-5.
  2. Rahman SMM, Hossain SM, Jahan M. Dengue fever: Bangladesh context. Editorial. BMRC Bulletin. 2019; 45:66-67
  3. Shirin T, Muraduzzaman AK, Alam AN, Sultana S, Siddiqua M, Khan MH, Akram A, Sharif AR, Hossain S, Flora MS. Largest dengue outbreak of the decade with high fatality may be due to reemergence of DEN-3 serotype in Dhaka, Bangladesh, necessitating immediate public health attention. New microbes and new infections. 2019: 29: 100511.
    DOI: 10.1016/j.nmni.2019.01.007.
  4. Mourão MPG, Lacerda Marcus VG, Bastos MS, Albuquerque BC, Alecrim WD. Dengue hemorrhagic fever and acute hepatitis: a case report. Brazilian Journal of Infectious Disease. 2004; 8: 461-64.
  5. Kumar R, Tripathi P, Tripathi S, Kanodia A, Venkatesh V. Preva KJK et al. Prevalence of dengue infection in north Indian children with acute hepatic failure. Ann Hepatol. 2008;7: 59-62.
  6. Rajat J, Bineeta K, Ranga GS, Kumar A. Dengue fever presenting as acute liver failure- a case report. Asian Pacific Journal of Tropical Medicine 2011: 323-24
  7. Kallenahalli Jagadish Kumar Kallenahalli JK, Shashirekha P, Vadambal GM and Umesh L. Dengue Hepatitis: A Case Report 2015.
    DOI: 10.5812/archcid.283756.
  8. Yudhishdran J, Navinan R, Ratnatilaka A, Jeyalakshmy S. Dengue haemorrhagic fever presenting with cholestatic hepatitis: two case reports and a review of literature. BMC Res Notes. 2014;7: 568. Published 2014:26.
    DOI: 10.1186/1756-0500-7-568.
  9. Poovorawan Y, Hutagalung Y, Chongsrisawat V, Boudville I, Bock HL. Dengue virus infection: a major cause of acute hepatic failure in Thai children. Ann Trop Paediatr. 2006;26:17-23.
  10. Syhavong B, Rasachack B, Smythe L, Rolain JM, Roque-Afonso AM, Jenjaroen K, et al. The infective causes of hepatitis and jaundice amongst hospitalised patients in Vientiane, Laos. Trans R Soc Trop Med Hyg. 2010;104:475-83.
  11. Souza LJ, Alves JG, Nogueira RM, Gicovate Neto C, Bastos DA, Siqueira EW, et al. Aminotransferase changes and acute hepatitis in patients with dengue fever: analysis of 1,585 cases. Braz J Infect Dis. 2004;8:156-63.3.
  12. Rosenthal D.S. Hematologic manifestations of infectious diseases. In: Hoffman R. eds. Hematology basic principles and practice. Orlando: Churchill Livingstone, 2000.
Correspondence: Arifa Akram
National Institute of Laboratory Medicine and Referral Center, Dhaka, Bangladesh
drbarna43@gmail.com
ORCID 0000-0001-8829-9817
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Submission
2020-07-16

Accepted
2020-11-12

Published
2020-12-01


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Issue
Vol 46 No 3 (2020)

Section
Case Report


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