|
| |
 |
|
| CASE REPORT |
|
| Year : 2019 | Volume
: 9
| Issue : 4 | Page : 194-198 |
|
Scrub typhus – A case series from the state of Sikkim, India
Aroop Mohanty1, Ankita Kabi2, Pratima Gupta1, Mithilesh Kumar Jha1, U Sasi Rekha1, Anusha Krishna Raj1
1 Department of Microbiology, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India
2 Department of Trauma and Emergency Medicine, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India
| Date of Submission | 14-Jun-2019 |
| Date of Decision | 05-Sep-2019 |
| Date of Acceptance | 16-Oct-2019 |
| Date of Web Publication | 11-Dec-2019 |
Correspondence Address:
Dr. Aroop Mohanty
Department of Microbiology, All India Institute of Medical Sciences, Rishikesh, Uttarakhand
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/IJCIIS.IJCIIS_50_19
 Abstract | | |
Scrub typhus is one of the leading causes of acute febrile illness in India. It is associated with rash and often an eschar, which responds dramatically to antibiotics. In some cases, it results in serious illness leading to multiple organ involvement and finally death. The various clinical manifestations of scrub typhus arise mainly due to systemic vasculitis, caused by direct effects of organism as well as exaggerated immune response. The disease course is often complicated, leading to mortality in the absence of treatment. Here, in this case series, we describe three cases depicting the typical manifestations which a patient of scrub typhus can present with highlighting the fact that high index of clinical suspicion is of utmost importance for this deadly disease.
Keywords: Acute kidney injury, atrial fibrillation, scrub typhus
How to cite this article:
Mohanty A, Kabi A, Gupta P, Jha MK, Rekha U S, Raj AK. Scrub typhus – A case series from the state of Sikkim, India. Int J Crit Illn Inj Sci 2019;9:194-8 |
How to cite this URL:
Mohanty A, Kabi A, Gupta P, Jha MK, Rekha U S, Raj AK. Scrub typhus – A case series from the state of Sikkim, India. Int J Crit Illn Inj Sci [serial online] 2019 [cited 2023 Mar 31];9:194-8. Available from: https://www.ijciis.org/text.asp?2019/9/4/194/272771 |
| Introduction | |  |
Scrub typhus is a life-threatening zoonosis caused by Orientia itsutsugamushi (formerly Rickettsia), an obligate intracellular Gram-negative bacterium, which was isolated in 1930. It is transmitted to human beings by the bite of a larval Leptotrombidium mite (chigger).[1] The target cells are the endothelial cells, monocytes, and other cell types, and the disease is associated with vasculitis and endothelial dysfunction. Illness varies from mild and self-limiting to fatal. After an incubation period of 6–21 days, onset is characterized by fever, rash, headache, myalgia, cough, and lymphadenopathy. Fewer than 50% of patients develop an eschar and <40% develop a rash. It is endemic to a geographically distinct region, the so-called tsutsugamushi triangle, which includes Japan, Taiwan, China, and South Korea. It also occurs in Nepal, Pakistan, Papua New Guinea, and Australian states. In India, initial reports appeared in the 1930s,[2] and a large number of cases were identified among troops during World War II in Assam and West Bengal.[3] Lately, it has been reported with increasing frequency from diverse ecologies, initially from southern India and later from the Himalayan belt, the plains of northern India, coastal areas, and even from metropolitan cities.[4],[5] The state of Sikkim situated in the Eastern Himalayas has a total geographic area of 7299 km2 and is essentially a mountainous region without flat piece of land of any extent anywhere. The mean annual rainfall is maximum in Gangtok (3494 mm) and is well distributed during the months from May to early October. Heavy rainfall and humid climate in these areas at lower altitudes are very conducive to the spread of arthropod vectors. The first outbreak of scrub typhus was reported in 2003–2004, when a cluster of pediatric patients presented with fever, hepatosplenomegaly, and eschar. Serological confirmation was done in the National Center for Disease Control, New Delhi. Despite a few studies done on this topic from this region, it is still being grossly underdiagnosed due to its nonspecific clinical presentation, limited public awareness, low index of suspicion among clinicians, and lack of diagnostic facilities in most places. We hereby present a case series showing the rare atypical clinical manifestations of scrub typhus from a tertiary care teaching hospital in Sikkim, India. These manifestations if present in a patient will help the clinicians in implementing a suspect and treat strategy and initiate proper treatment to prevent serious morbidity and fatality in this potentially treatable and curable disease.
| Case Reports | | |
Case 1
A 2-year-old male child presented to the Department of Pediatrics of our institute with fever associated with chills for 6 days, decreased urine output for 4 days, progressive abdominal swelling associated with loose stools for 3 days, and nonproductive cough for 2 days and was hospitalized. Physical examination revealed a febrile child with pallor, periorbital puffiness, pedal edema, hepatomegaly, evidence of free fluid in abdomen, and bilateral pleural effusion. Injection ceftriaxone 50 mg/kg/day was given for 3 days empirically along with supportive treatment, but the child did not improve. Antistreptolysin O test was done in order to rule out poststreptococcal glomerulonephritis which was negative. A brownish-black-crusted lesion with surrounding erythema-eschar was found below the left axilla [Figure 1]. Blood samples were sent for routine investigations. Complete blood count (CBC) revealed hemoglobin (Hb) of 9.9 g/dl, Total leucocyte count (TLC) of 6600/mm3, polymorph (85%), and platelets of 90,000/mm3. The urine analysis indicated proteinuria, microscopic hematuria, and red blood cell casts. Blood urea (43 mg/dl) and serum creatinine (1.6 mg/dl) were raised. The liver function tests revealed transaminitis and cholestasis (alanine aminotransferase [ALT] 148 IU/L and aspartate aminotransferase [AST] 161 IU/L). The kidney function also was deranged with sodium (43 mg/dl) and potassium (7.8 mg/dl). The chest X-ray view confirmed bilateral pleural effusion [Figure 2]. Ultrasound (USG) of abdomen and pleural spaces revealed ascites with hepatosplenomegaly and bilateral pleural effusion. Widal test was negative. Hepatitis B virus surface antigen and anti hepatitis C virus were negative. A diagnosis of scrub typhus complicated with acute kidney injury (AKI) was made based on the basis of clinical findings, laboratory results, and positive Weil–Felix test and IgM ELISA. Tablet doxycycline 2.2 mg/kg/day was given for 3 days, and by 6th day of admission, the child became afebrile, with regression of edema and was discharged home on the 10th day.
Case 2
A 53-year-old male presented to the Emergency Department of our Institute with fever, headache, vomiting, and altered consciousness for the last 2 days. The informant was his son with fair reliability. The fever was initially low grade but had become high grade and was associated with chills and rigors. He developed confusion and disorientation a day 2 days before hospitalization. There was no history of seizures, cough, or dysuria or rashes. He was a known hypertensive on regular medications. He was a teetotaler and nonsmoker. On examination, the patient was disoriented to time, place and person, was febrile, and had blood pressure (BP) record of 170/100 mmHg. He did not have any icterus, rashes, or signs of meningeal irritation. Cranial nerve examination revealed no deficit except bilateral papilledema. Other systemic examinations were normal. Investigations revealed normal urine routine examination. CBC revealed TLC of 14,230/cmm polymorph 85%, with normal Hb and platelets. The liver function tests revealed transaminitis and cholestasis (ALT 99U/L, AST 122U/L, Gamma glutamyl transferase (GGT) 300 U/L, and alkaline phosphatase of 304 U/L). USG of the abdomen revealed mild hepatosplenomegaly. Chest X-ray view was normal. Leptospira Microscopic agglutination test (MAT) was negative. Noncontrast computed tomography scan of head revealed features of early cerebral edema. Cerebrospinal fluid (CSF) studies revealed glucose 45 mg/dL, protein of 78 mg/dL, cells of 202/cmm with lymphocytic predominance, negative for acid-fast bacilli, and adenosine deaminase of 5 U/L, and GeneXpert was negative. CSF viral antibodies for Herpes simplex virus and Japanese encephalitis were negative. IgM for scrub on day 2 of hospitalization was 1.25 (normal range <0.14). He was treated with parenteral doxycycline (5 mg/kg twice daily × 7 days), mannitol (100 g/24 h), and levetiracetam (500 mg twice daily × 2 weeks). He improved slowly, and a repeat investigation after 1 week revealed a normal CSF study, a normal MRI brain and an IgM scrub titer of 1.68. He improved slowly but completely and was discharged after total 2 weeks hospitalization.
Case 3
A 45-year-old male who was previously well presented to the Emergency Department of our institute with complaints of fever, shortness of breath, and cough with scanty expectoration for the last 7 days. The fever was high grade in nature and was occasionally associated with chills and rigors. He was referred from a nearby private nursing home where he was admitted for the last 3 days. During his stay there, he developed aphasia and shortness of breath. There was no history of any seizure, rashes, weakness, or hematuria. The patient was a chronic smoker for the past 20 years. On examination, he was conscious, alert, and oriented. He was febrile and had a heart rate of 120 beats/min, respiratory rate 44 breaths/min, and BP 90/60 mmHg. The pulse was irregularly irregular. On systemic examination, bilateral coarse crepitations were present in lung bases on auscultation. Other examinations were within normal limits. A provisional diagnosis of acute febrile illness was made with an incidental finding of atrial fibrillation (AF). Cardiology opinion was sought for the same. The patient consent was obtained for Direct current (DC) cadioversion, and a shock of 200 joules was given. The rate was brought in control, but the AF could not be reverted back. Injection amiodarone 150 mg was given immediately and then tapered at regular intervals. Blood samples were sent for routine investigations. CBC revealed TLC of 15,400/cmm polymorph 87%, with normal Hb and platelets. The liver function tests were within normal limits. Dengue serology and malarial antigen came negative. Cultures from blood and urine were sterile. Weil–Felix test was positive and IgM antibody for scrub typhus was strongly positive (by ELISA). The patient was reexamined thoroughly and an eschar was found on the back of the neck confirming the diagnosis [Figure 3]. He was started on tablet doxycycline (100 mg twice a day) for 7 days. He responded to doxycycline, and within 48 h, his symptoms decreased significantly and her vitals steadily improved. The patient's condition improved gradually, and he was discharged after 2 weeks.
| Discussion | | |
Rickettsial infections are emerging as pathogens around the world in areas which were hitherto unaffected. The rickettsial diseases were once thought to have disappeared from India, but cases are reemerging from several parts of the country. Scrub typhus is now most commonly reported rickettsial infection from the Indian subcontinent. The diagnosis of scrub typhus is made by using Faine's criteria, with proper history, epidemiological data, occupational history, clinical examination, seasonal variation, and laboratory support. In India, scrub typhus cases have been regularly reported from Vellore and Tamil Nadu.[5] There are scanty reports of scrub typhus from Sikkim state.[6],[7] Darjeeling is one of the endemic areas of scrub typhus until 1960, thereafter no outbreak was there. In 2005, cases are being reported. Sikkim has annual rainfall of 429–666 mm.[8] Vegetation in Sikkim also favors the chiggers to attach with rodents during monsoon season.[9] The outbreaks are associated with the predominance of the vector Leptotrombidium deliense, but recently, there has been an important observation L. deliense was missing, and there is emergence of Schoengastiella ligula, as the primary vector in the outbreak of Kurseong district of West Bengal.[10] Mahajan et al. have reported the presence of eschars in 7%–97% of scrub typhus cases in Japan.[11]
Multiple eschars have been reported in a single patient.[12] In our case, a diligent search for skin rashes helped in finding an eschar and later helped in diagnosis. The majority of studies regarding rickettsial infections from various parts of the world are based on the adult populations [Table 1].[13] There is a paucity of studies regarding the incidence and clinical profile of scrub typhus in children of scrub typhus. Scrub typhus is regarded as a life-threatening disease in children.
The complications of scrub typhus are pneumonia, acute respiratory distress syndrome, acute hepatitis, AKI, meningitis, pancreatitis, acalculous cholecystitis, axonal polyneuropathy, long-segment myelitis, Disseminated intravascular coagulation (DIC), septic shock, and multiple organ dysfunction syndrome.[14],[15],[16],[17] In our cases, patients presented with complications with short incubation time. In the Indian scenario, there is a higher case fatality of 14% when presenting with complications.[17] In a study conducted in Meghalaya, only 11.1% patients had eschar and 33.3% of patients presented with complications with high mortality.[18] There is need to assess for the predictors of mortality such as BP, liver enzymes, platelet count, respiratory effort, and serum urea and creatinine in such scenario. The doubling time for scrub typhus is 9–18 h, so it takes 4 weeks for the culture to become positive.[19] Nested Polymerase chain reaction (PCR) from the eschar samples or buffy coat can help in early diagnosis of the disease within the first 3 days of fever onset even before the appearance of antibodies.[20]
Rickettsial infections have been overlooked as a cause of AKI, especially in children. A recent retrospective study from Central India did not report any case of AKI in children with Rickettsial infections.[21] Several studies have reported lower incidences of AKI ranging from 2% to 10%. According to Yen et al. scrub typhus presented with symptoms of acute renal failure is a rare but a serious condition.[22] The mechanism of AKI in scrub typhus is mainly believed to be impaired renal perfusion due to volume depletion or increased vascular permeability. Overall, renal involvement is considered to be a part of multiorgan dysfunction in patients with severe disease.[4]
Acute myocarditis is associated with scrub typhus more common than previously reported. Patients with high bilirubin and paroxysmal AF are at increased risk of acute myocarditis with scrub typhus, and hence, these patients should be evaluated for cardiac complications when presented with scrub typhus.[23] The management includes supportive therapy intravenous fluid replacement therapy, mechanical ventilation, and intravenous antibiotics, with the addition of tablet doxycycline 100 mg twice daily for 7 days.[24],[25],[26],[27],[28],[29]
| Conclusion | | |
Scrub typhus has been underdiagnosed in India due to its nonspecific clinical presentation, limited awareness and low index of suspicion among clinicians, and lack of diagnostic facilities. The clinical manifestations of scrub typhus in children are nonspecific and are likely to be misdiagnosed. Scrub typhus does not find a mention in most descriptions of tropical community-acquired AKI or acute myocarditis. Considering the reemergence of scrub typhus in India, patients presenting with fever and AKI as well as rhythm abnormalities should be investigated for scrub typhus. Early diagnosis of scrub typhus and the initiation of empirical therapy with doxycycline will reduce patient morbidity and mortality.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed. The authors followed applicable EQUATOR Network (http://www.equator-network.org/) guidelines during the preparation of this report.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
| References | | |
| 1. | Weitzel T, Dittrich S, López J, Phuklia W, Martinez-Valdebenito C, Velásquez K, et al. Endemic scrub typhus in South America. N Engl J Med 2016;375:954-61.  |
| 2. | Roy BC. Typhus fever; with special reference to its incidence in India. J Indian Med Assoc 1945;15:135-46. |
| 3. | Sayen JJ, Pond HS, Forrester JS, Wood FC. Scrub typhus in Assam and Burma; a clinical study of 616 cases. Medicine (Baltimore) 1946;25:155-214. |
| 4. | Mathai E, Rolain JM, Verghese GM, Abraham OC, Mathai D, Mathai M, et al. Outbreak of scrub typhus in Southern India during the cooler months. Ann N Y Acad Sci 2003;990:359-64. |
| 5. | Mahajan SK, Rolain JM, Kashyap R, Bakshi D, Sharma V, Prasher BS, et al. Scrub typhus in Himalayas. Emerg Infect Dis 2006;12:1590-2. |
| 6. | Aggarwal P, Mahesh DM, Ravi Kumar V, Himral P, Kaushal SS, Verma BS. Atypical Eschar sites in scrub typhus in sub-Himalayas. J Assoc Physicians India 2009;57:154. |
| 7. | Tilak R. Ticks and mites. In: Bhalwar RV, editor. Textbook on Public Health and Community Medicine. 131 st ed. Pune: Department of Community Medicine, AFMC; 2009. p. 955-9. |
| 8. | |
| 9. | Frances SP, Watcharapichat P, Phulsuksombati D, Tanskul P, Linthicum KJ. Seasonal occurrence of Leptotrombidium deliense (Acari: Trombiculidae) attached to sentinel rodents in an orchard near Bangkok, Thailand. J Med Entomol 1999;36:869-74. |
| 10. | Tilak R, Kunwar R, Wankhade UB, Tilak VW. Emergence of Schoengastiella ligula as the vector of scrub typhus outbreak in Darjeeling: Has Leptotrombidium deliense been replaced? Indian J Public Health 2011;55:92-9. [ PUBMED] [Full text] |
| 11. | Mahajan SK. Scrub typhus. J Assoc Physicians India 2005;53:954-8. |
| 12. | Gurung S, Pradhan J, Bhutia PY. Outbreak of scrub typhus in the North East Himalayan region-Sikkim: An emerging threat. Indian J Med Microbiol 2013;31:72-4. [ PUBMED] [Full text] |
| 13. | Sayen JJ, Pond HS. Scrub typhus in Assam and Burma; a clinical study of 616 cases. Medicine (Baltimore) 1946;25:155-214. |
| 14. | Dhakal M, Dhakal OP, Bhandari D. Pancreatitis in scrub typhus: A rare complication. BMJ Case Rep 2014;2014. pii: bcr2013201849. |
| 15. | Tandon R, Kumar A, Kumar A. Long-segment myelitis, meningoencephalitis, and axonal polyneuropathy in a case of scrub typhus. Ann Indian Acad Neurol 2019;22:237-40. [ PUBMED] [Full text] |
| 16. | Chi WC, Huang JJ, Sung JM, Lan RR, Ko WC, Chen FF. Scrub typhus associated with multiorgan failure: A case report. Scand J Infect Dis 1997;29:634-35. |
| 17. | Yi SY, Tae JH. Pancreatic abscess following scrub typhus associated with multiorgan failure. World J Gastroenterol 2007;13:3523-5. |
| 18. | Sivarajan S, Shivalli S, Bhuyan D, Mawlong M, Barman R. Clinical and paraclinical profile, and predictors of outcome in 90 cases of scrub typhus, Meghalaya, India. Infect Dis Poverty 2016;5:91. |
| 19. | Tamura A, Ohashi N, Urakami H, Miyamura S. Classification of Rickettsia tsutsugamushi in a new genus, Orientia gen. Nov. as Orientia tsutsugamushi comb. Nov. Int J Syst Bacteriol 1995;45:589-91. |
| 20. | Kim DM, Kim SW, Choi SH, Yun NR. Clinical and laboratory findings associated with severe scrub typhus. BMC Infect Dis 2010;10:108. |
| 21. | Rathi NB, Rathi AN, Goodman MH, Aghai ZH. Rickettsial diseases in central India: Proposed clinical scoring system for early detection of spotted fever. Indian Pediatr 2011;48:867-72. |
| 22. | Yen TH, Chang CT, Lin JL, Jiang JR, Lee KF. Scrub typhus: A frequently overlooked cause of acute renal failure. Ren Fail 2003;25:397-410. |
| 23. | Chin JY, Kang KW, Moon KM, Kim J, Choi YJ. Predictors of acute myocarditis in complicated scrub typhus: An endemic province in the republic of Korea. Korean J Intern Med 2018;33:323-30. |
| 24. | Takhar RP, Bunkar ML, Arya S, Mirdha N, Mohd A. Scrub typhus: A prospective, observational study during an outbreak in Rajasthan, India. Natl Med J India 2017;30:69-72. [ PUBMED] [Full text] |
| 25. | Khan SA, Bora T, Laskar B, Khan AM, Dutta P. Scrub typhus leading to acute Encephalitis syndrome, Assam, India. Emerg Infect Dis 2017;23:148-50. |
| 26. | Rizvi M, Sultan A, Chowdhry M, Azam M, Khan F, Shukla I, et al. Prevalence of scrub typhus in pyrexia of unknown origin and assessment of interleukin-8, tumor necrosis factor-alpha, and interferon-gamma levels in scrub typhus-positive patients. Indian J Pathol Microbiol 2018;61:76-80. [ PUBMED] [Full text] |
| 27. | Oberoi A, Varghese SR. Scrub typhus-an emerging entity: A study from a tertiary care hospital in North India. Indian J Public Health 2014;58:281-3. [ PUBMED] [Full text] |
| 28. | Peesapati N, Lakkapraga R, Sunitha S, Sivaram PV. Clinical manifestations and complications of scrub typhus: A hospital-based study from North Andhra. J Assoc Physicians India 2019;67:22-4. |
| 29. | Bhargava A, Kaushik R, Kaushik RM, Sharma A, Ahmad S, Dhar M, et al. Scrub typhus in Uttarakhand & adjoining Uttar Pradesh: Seasonality, clinical presentations and predictors of mortality. Indian J Med Res 2016;144:901-9. [ PUBMED] [Full text] |
[Figure 1], [Figure 2], [Figure 3]
[Table 1]
| This article has been cited by | | 1 |
Revisiting Scrub typhus: A neglected tropical disease |
|
| Mini Bhandari, Rahul Kunwar Singh, Alexey Laishevtcev, Tribhuvan Mohan Mohapatra, Manisha Nigam, Edna Mori, Bruna Caroline Gonçalves Vasconcelos de Lacerda, Henrique Douglas Melo Coutinho, Abhay Prakash Mishra | | Comparative Immunology, Microbiology and Infectious Diseases. 2022; : 101888 | | [Pubmed] | [DOI] | | | 2 |
Scrub Typhus Co-Infections in a Young Boy With Varicella and Malaria: A Rare Case Report |
|
| Khushbu Pandey, Aroop Mohanty, Monika Matlani, Mamta Ahir, Vivek Hada | | Cureus. 2022; | | [Pubmed] | [DOI] | |
|
 |
|
|
|
