Research Article
Scrub Typhus Case from Myanmar Complicated by Bilateral Frontoparietal Cortical Infarcts
Ohnmar Ohnmar, Department of Neurology, Yangon General Hospital, University of Medicine, Yangon, Myanmar.
Corresponding Author: Ohnmar Ohnmar*, Zin Nwe Win, Myat Kyaw and Thandar Lwin
Received: September 16, 2021; Revised: October 11, 2021; Accepted: October 13, 2021 Available Online: November 11, 2021
Citation: Ohnmar O, Win ZN, Kyaw M & Lwin T. (2022) Scrub Typhus Case from Myanmar Complicated by Bilateral Frontoparietal Cortical Infarcts. J Neurosurg Imaging Techniques, 7(3): 503-506.
Copyrights: ©2022 Ohnmar O, Win ZN, Kyaw M & Lwin T. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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A previously healthy 69-year-old agricultural man presented with prolonged fever, thrombocytopenia, acute hepatitis, acute kidney failure and acute bilateral fronto-parietal cortical infarcts. Screening tests for common systemic infections which can cause such multisystem involvement such as malaria, leptospirosis was negative. There was no eschar, rash or lymphadenopathy. Although being locally unavailable, rickettsia serology was finally sent to overseas laboratory and scrub typhus serology turned out to be positive. He significantly improved after intravenous azithromycin. At one-month after treatment initiation, he was completely back to normal. Here we report a case of scrub typhus in a resource-poor setting of Myanmar complicated with acute cerebral infarction which was not commonly reported.

Keywords: Scrub typhus, Cerebral infarct, Myanmar.
Scrub typhus (ST) caused by Orientia tsutsugamushi, transmitted by trombiculid mites (chigger’s bite), is endemic in tsutsugamushi triangle in the Asia-Pacific area. Mortality can be as high as 30% without proper treatment [1]. It infects endothelial cells affecting all organs [2]. There is a wide spectrum of neurological manifestations, among which meningoencephalitis is classical [3]. Stroke cases mainly intracranial hemorrhage [4] were reported and acute cerebral infarct is one of the less common complications of ST.

A 69-year-old man, an agricultural worker lived in a village near Pyay town in Bago Province, a non-drinker and non-smoker, was admitted to Sakura hospital with one-month prolonged fever, five days of jaundice, and three days of anuria, confusion and weakness of all four limbs. There was no history of seizures, headache and vomiting before. Fever was high up to 40°C, remittent, not associated with chills and rigors, rash, cough, dysuria, diarrhea or abdominal pain. He was already treated at local clinics and hospital with various antibiotics but referred to our hospital after a month because of persistent fever and worsening general condition with confusion. His past medical history was unremarkable. No febrile illness reported in the family. On examination, he had fever, conjunctival edema, pallor, jaundice, Glasgow Coma scale (GCS) 11 (E3V3M5), with stable vitals. There was no meningism, no cranial neuropathy but he had hypertonia and hyperreflexia with bilateral extensor plantar responses. Other systemic examination was normal except mild hepatomegaly. No eschar, rash or lymphadenopathy were noted. ECG and chest X-ray were unremarkable. Baseline blood tests on admission showed random blood sugar 429 mg%, hemoglobin 5.8 g/dL, WBC 25.88 x 109/L, absolute neutrophil 86.8%, lymphocyte 10.2%, platelet count 63 x 109/L, erythrocyte sedimentation rate 35 mm/1st hour, C reactive protein 80.89 mg/L, creatinine 804umol/L, urea 430 mmol/L, sodium 177mmol/L, potassium 5.6mmol/L, chloride 145mmol/L, bicarbonate 12.3mmol/L, serum bilirubin 44.46umol/L, alkaline phosphatase 122 U/L, ALT 195 U/L and AST 175 U/L, gamma GT 128 U/L, HbA1c 5.7%. serum amylase 126.6, PT 12.7 seconds, INR 1.08, APTT 28.4 seconds, D-dimer 3711.6 ng/mL, fibrinogen 7520 mg/dL. Widal test, malaria blood film, dengue and Chikungunya serology, leptospiral serology, HIV, HBs antigen, anti-HCV antibodies, Quantiferon-TB Gold plus ELIZA and syphilitic screening were all negative. Stool and urine routine examination were normal. Urine, sputum and blood cultures were sterile. Abdominal ultrasound showed acute hepatitis with splenomegaly. Echocardiogram did not reveal any vegetation. Non-contrast CT (Head) scan was normal. Electroencephalography showed mild diffuse encephalopathy with diffuse theta slowing at bilateral frontoparietal regions without clinical or electrographic seizures. MRI showed gyri form pattern of restricted diffusions without susceptibility consistent with acute bilateral frontoparietal cortical infarcts (Figure 1).

MRA revealed normal major intracranial arteries and MRV was normal. Cerebrospinal fluid study was normal. Differential diagnoses on admission were Weil’s disease or severe falciparum malaria. He was treated with insulin, hydration, correction of electrolyte imbalance, anti-malaria treatment and various empirical antibiotics including intravenous ceftriaxone, levofloxacin, vancomycin, piperacillin/tazobactam and metronidazole for persistent high fever. Finally, his fever subsided after intravenous azithromycin for five days. Rickettsia serology (indirect fluorescent antibody test) was sent late to overseas laboratory after 6 weeks from onset of fever and scrub typhus serology turned out to be positive with IgM 1:800, IgG 1:400 while murine and tick typhus serologies were negative. His neurological status returned back to normal completely with normal blood parameters including platelet count, renal and liver functions in 4 weeks after initiation of azithromycin.

We presented a case of ST that was diagnosed late, besides suffered from acute ischemic small vessel infarcts and multiorgan failure, and recovered after treatment without sequelae. While diagnosis is to be based on history of exposure, clinical features and serological test, it was late in current case because of absence of eschar, which is a necrotic skin lesion at the site of a chigger mite bite, and low index of clinical suspicion by attending doctors. Although being endemic, ST is not as well-known as malaria, typhoid, dengue and leptospirosis in our country, the reason for which might be poor awareness due to lack of local diagnostic facilities and few published studies and case reports from Myanmar on it. In 1947, Davis GE first documented about ST in Myanmar [5]. Thailand published studies on ST cases at Thai-Myanmar border 2003 and 2017 [6,7]. Japan published a case with ST imported from Myanmar in 2009 [8]. There was a case report on two Indian soldiers who contracted ST after travel to Indo Myanmar border in 2015 [9]. In 2020, first Myanmar group led by Win did serologic and molecular surveillance on clinically suspected ST cases in Sagging and Magway Provinces (central Myanmar) and affirmed genetic heterogeneity and endemicity of ST in Myanmar [10]. Recently Elders et al studied seroprevalence at various parts of Myanmar and concluded that the widespread distribution of rickettsioses in Myanmar was particularly high in central and northern regions [11]. However, our case was from Bago province in Southern Myanmar. Apart from above few studies, there were scarce literature and reports of ST from Myanmar [1]. Our case agrees with the findings of the 14-year study in Laos on spatial and temporal distributions of ST, which concluded that ST is more common in rural area, and visiting rice fields and forests with surface flooding and high vegetation density poses higher risk of getting it [12]. Wilairatana [13] reviewed that malaria and scrub typhus co-infection was high in endemic areas such as India (8%) and Thailand (35%) among febrile patients. However, malaria tests (blood film and ICT) were negative in our case so co-infection was unlikely although both are undeniably endemic in Myanmar [13]. There has been no case report on its CNS sequelae in Myanmar yet. Ischemic stroke complication was reported only in few cases, presenting with both small vessel [14,15] and large vessel infarcts [16]. Pathogenesis of bilateral cortical infarcts in the presence of normal INR and APTT and normal MRA in our case can be explained by widespread cerebrovascular endothelial dysfunction and vasculitis in small vessels due to direct invasion of endothelium by rickettsia, which is the main pathologic findings described in ST cases [1]. Our case is also in accordance with previous case reports where stroke complicated cases were those who received delayed effective antibiotics after onset [16]. Although being life-threatening with severe hepatorenal failure in addition to multiple infarcts, our case, on receiving appropriate antibiotics which was inexpensive and easily available, fully recovered. So, it is essential to have high index of clinical suspicion and to establish easily accessible testing facility since ST is not susceptible to routinely and empirically used β-lactam-based regimens. In conclusion, ST should be one of the differentials not to be overlooked in febrile patients from rural areas of Myanmar.


Written informed consent was obtained from the patient’s family.
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