https://imcjms.com Ibrahim Medical College Journal of Medical Science https://imcjms.com/registration/journal_full_text/247 Mon, 10 Jul 2017 09:06:34 +0000 Melioidosis, caused by Burkholderia pseudomallei, is a potentially fatal infectious disease. Early and correct diagnosis is important, as mortality in untreated melioidosis is high. The first case of melioidosis from Bangladesh was reported in 1988. Since then a few cases have been reported from Bangladesh. We report here four culture confirmed cases of melioidosis diagnosed in BIRDEM Genaral Hospital during May 2009 to April 2010.The detail demographic data, clinical features and outcome are discussed. We have also reviewed all the melioidosis cases among Bangladeshi population recorded from 1988 to 2014. Ibrahim Med. Coll. J. 2014; 8(1): 25-31 Address for Correspondence: Prof. Jalaluddin Ashraful Haq, Professor, Department of Microbiology, Ibrahim Medical College, 122 Kazi Nazrul Islam Avenue, Shahbag, Dhaka, Bangladesh. e-mail: jahaq54@yahoo.com     Melioidosis is an emerging infection in Bangladesh. It is a disease caused by Burkholderia pseudomallei, a Gram-negative bacterium, found in wet soil, mud and pooled surface water in the tropics and subtropics. It is endemic in many countries of the world.1 Documented reports of melioidosis from Bangladesh have been few and sporadic. The first culture proven case was reported from Bangladesh in 1988.2 Later on, in 2001 another case of melioidosis in an adult with diabetes mellitus was reported from BIRDEM hospital.3 Mortality associated with this infection is high and early diagnosis and specific antimicrobial therapy can minimize the fatal outcome.4-6 Therefore, awareness regarding the disease and correct identification of the offending organism is important.   A 60-year-old diabetic (Type 2) male from Tangail district presented with persistent high-grade fever and burning sensation during micturation for two months. He was initially treated for these complains in the local district hospital with intravenous ceftriaxone for 12 days, but fever did not subside. So, he was admitted in BIRDEM Genaral Hospital on 3rd November 2009 for better management. He had a history of successfully treated pulmonary tuberculosis ten years ago. Physical examination revealed low-grade fever. Spleen, liver and lymph nodes were not palpable. There was no documentation of per rectal examination of prostate of this patient. His total leucocyte count was 10x109/L with a shift to left, ESR 150 mm in 1st hour, HbA1c 10.0%, fasting blood glucose 15.3 mmol/L. Other biochemical parameters were within normal limits. Ultrasound showed enlarged prostate with prostatic abscess involving left seminal vesicle and cystitis (Figure-1). Routine urine investigations revealed pyuria. Culture of the midstream urine grew oxidase positive, lactose fermenting gram-negative bacilli, which were identified as Burkholderia pseudomallei by standard biochemical test. The strain was resistant to gentamicin, netilmicin, aztreonam, cefotaxime, colistin and sensitive to ceftazidime, ceftriaxone, ciprofloxacine, cotrimoxazole, piperacillin and imipenem. Subsequently, transurethral resection of prostate (TURP) with endoscopic drainage of prostatic abscess was done. Pus and tissue were sent for further evaluation. Histopathology report revealed acute and chronic prostatitis with abscess. Pus from abscess yielded growth of B. pseudomallei. The antibiotic sensitivity pattern was same as the strain isolated previously from urine. He was treated with intravenous ceftazidime 1gm 8 hourly for four weeks and oral co-trimoxazole (800/160mg) twice daily. He was discharged after remission of fever and improvement of overall condition with advice to continue cotrimoxazole twice daily for a period of six months. On follow up after one month and six months after  discharge, he was asymptomatic and his urine culture showed no growth.            Figure-1: Ultrasonography of prostate showing enlarged prostate with multiple hypoechoic areas suggestive of abscess.  Left seminal vesicle was enlarged and loculated (Case -1) Case 2 (2009)   On 16th January 2010, a 41 years old diabetic man from Gazipur district presented to BIRDEM General Hospital with painful right ankle joint, three months history of low grade fever, weight loss and burning micturation for 4 days. He had been admitted in our hospital one month ago for similar pain in right ankle joint and was then diagnosed as a case of reactive arthritis with hyponatraemia and treated accordingly. At that time culture of urine was yielded no growth though pyuria was noted in routine microscopy of urine. Physical examination revealed low grade fever with tender and swollen right ankle joint. Liver and spleen was normal. There was no documentation of per rectal examination of prostate. Investigation revealed total leucocyte count 7.5x109/L with a shift to left, ESR 130 mm in 1st hour, HbA1c 7.1%, fasting blood glucose 14.1 mmol/L and serum uric acid 2.9 mg/dl. The plain x-rays of right ankle joint were normal but USG of whole abdomen showed prostatic abscess (11x23mm;  Figure-3)) and cholelithiasis. Urine microscopy showed pyuria and on culture B. pseudomallei grew, which was sensitive to ceftazidime, augmentin, cotrimoxazole, imipenem and resistant to amikacin, netilmicin, gentamicin, ciprofloxacin, polymixin B. He was treated for  45 days with intravenous ceftazidime 2 gm 8 hourly, followed by oral cotrimoxazole (800/160mg) twice daily for 20 weeks. The prostate abscess was not drained. He made a good recovery, remained well six months after discharge.     Figure-3: Ultrasonography of prostate showing multiple hypoechoic areas suggestive of abscess (Case 3)   In 23rd January 2010, a 41 years old diabetic female from Savar, (about 27 km north of Dhaka city) presented with 20 days history of fever, cough, and breathlessness. Prior to admission in BIRDEM hospital on 23rd January’15, she was diagnosed as a case of diabetes mellitus with ketoacidosis and lung abscess in another hospital and was treated with intravenous ceftriaxone and levofloxacine. After recieving antibiotics for twelve days she continued to remain febrile, hence she was referred to our hospital. Physical examination was unremarkable. X-ray chest (P/A view) revealed a large lung abscess in right upper lobe (Figure-4). Sputum examination was negative for AFB. Blood analysis yielded haemoglobin 8.9 g/dl, total leucocyte count 8.23x109/L with neutrophil 77%, ESR-120 mm in 1st hour, HbA1c 15%, blood glucose  2 hours after breakfast 9.2 mmol/L, serum cholesterol 202 mg/dl, triglyceride 144 mg/dl. Blood and urine culture were negative, but sputum culture yielded growth of B. pseudomallei which was sensitive to ceftazidime, tetracycline, augmentin, cefotaxime, imipenem but resistant to ciprofloxacin, cotrimoxazole, aminoglycosides and polymyxin B. She was treated with intravenous ceftazidime (120 mg/kg/day) and oral doxycycline 200 mg twice daily for initial one month. The patient showed marked clinical, microbiological and radiological improvement in one month. She was discharged with oral doxycycline 200 mg twice daily for six months.     Fig-4: X-ray chest (P/A view) showing large lung abscess in right upper lobe (Case 4) All four cases were culture confirmed (Figure-5) chronic suppurative form of melioidosis involving different organs of the body. The demographic data, clinical feature and outcome of the four cases described above are summarized in Table-1.     Figure-5:  Culture shows the growth of B. pseudomallei in Blood (left) and MacConkey (Right) agar plates. Note the shiny metallic texture of the colonies. Fig.6: Map showing geographical distribution of all recorded melioidosis cases in Bangladesh from 1988 to 2014. Table-1: Summary of four cases of melioidosis described above   Melioidosis, caused by B. pseudomallei, was first reported from our neighboring Rangoon in 1912. Since then, many cases of melioidosis have been reported in India, Srilanka, Thailand, Malaysia and many other countries of the world. Though Bangladesh has similar environmental and climatic conditions, only two cases of culture confirmed melioidosis have so far been reported during the period from 1988 to 2009.2-3  Other six  cases of melioidosis were reported among immigrant Bangladeshi population in UK between 1991 to 1999 (Table-2).7-9 In 2007, a 90 years old Belgium traveler developed melioidosis after visiting Rangpur district of Bangladesh several times particularly in rainy months of the year.10  Table-2: Cases of melioidosis recorded among local and immigrant Bangladeshi population from 1988 to 2014 (Total cases - 15)   The presentation of melioidosis ranges from localized to systemic infection. Infection by the causative agent B. pseudomallei causes abscess formation in different organs of the body, which includes lung, liver prostate and soft tissues.11-13 It presents as a febrile illness, ranging from acute fulminent septicemia to a chronic, debilitating localized infection. About 18% of adult males with melioidosis in North Australia had prostate abscess compared with fewer than 2% in Thailand.14 The lung is another most commonly affected organ in melioidosis, which can present as acute or chronic pneumonia to abscess formation.15 In our fourth case, cavitary lesion with large lung abscess in right upper lobe was seen in chest X-ray. Cavitary lesions may sometimes mimic the lesion seen in pulmonary tuberculosis, but diagnosis of melioidosis was demonstrated by isolation of B. pseudomallei from the sputum culture. Melioidosis is most commonly associated with underlying diseases like diabetes mellitus, renal disease and immunodeficiency disorders.4-6 Of these, diabetes is the most common risk factor,7,8 as was seen in our all four patients (Table-1). The estimated relative risk of melioidosis for diabetic patients was 13.1% in Australia.4 Table-1 summarizes the presentation and organ involvement in four cases of melioidosis. We have reviewed all known or reported cases of melioidosis detected in Bangladesh from 1988 to 2014. Altogether nineteen melioidosis cases (4 in Table 1 and 15 in Table 2) have so far been recorded either amongst the local or migrated Bangladeshi population. Out of nineteen cases, five cases of melioidosis were detected and reported from UK among Bangladeshi immigrant as ‘imported cases’7-9 while one was a 90 years-old Belgium traveler who stayed in northern district of Bangladesh (Rangpur) for sometime on several occasions.10 Table-2 summarizes the clinical features and other epidemiological data of all those cases. Apart from the four cases described above, we have detected six more cases in BIRDEM General Hospital within the period from 2010 to 2014 (Table-2). Out of nineteen cases, majority had abscess in different parts or organs of the body while some developed septicemia. Even though the presentation of those cases varied but majority had diabetes mellitus as an underlying disease and risk factor. Out of nineteen recorded cases, few died which indicate that the outcome is favourable with correct and timely diagnosis of the condition. The cases described and reviewed above indicate that melioidosis is endemic in Bangladesh particularly in north and northeastern districts of the country. Physicians and medical microbiologists should investigate for this important infection when diabetic patients, especially from endemic zone, present with characteristics clinical features. The prevalence of melioidosis is probably underestimated due to the lack of awareness among the microbiologists and doctors of the country about the disease. The true incidence of the disease in Bangladesh may actually be much higher than is currently believed. Therefore, systematic study is needed to determine the actual extent of the disease. Rererences 2.    Struelens MJ, Mondol G, Bennish M, Dance DAB. Melioidosis in Bangladesh: a case report. Trans R Soc Trop Med Hyg 1988; 82: 777-778. 4.    Cheng AC, Currie BJ. Melioidosis: epidemiology, pathophysiology and management. Clin Microbiol Rev 2005; 18(2): 383-416. 6.    Jilani MSA, Haq JA. Melioidosis in Bangladesh- a disease yet to be explored. Ibrahim Med Coll J 2010; 4(1): i-ii. 8.    Hoque SN, Minassin M, Clipstone S, Lloyd-Owen SJ, Sheridan E, Lessing MPA. Melioidosis presenting as septic arthritis in Bengali men in East London. Rheumatology 1999; 38(10): 1029-1031. 10.  Ezzedine K, Malvy D, Steels E, De Dobbeeler G, Struelens M, Jacobs F, Heenen M. Imported melioidosis with an isolated cutaneous presentation in a 90-year-old traveler from Bangladesh. Bull Soc Pathol Exot 2007; 100(1): 22-25. 12.  Vidyalakshmi K, Shrikala B, Bharathi B, Suchitra U. Melioidosis: an under diagnosed entity in western costal India: a clinico-microbiological analysis. Indian J Med Microbiol 2007; 25(3): 245-8. 14.  Ng TH, How SH, Amran AR, Razali MR, Kuan YC. Melioidotic prostatic abscess in Pahang. Singapore Med J 2009; 50(4): 385-389. 16.  Raja NS, Ahmed MZ, Singh NN. Melioidosis: An emerging infectious disease. J Postgrad Med 2005; 51(2): 140-144. 18.  Majumder MI, Haque MM, Ahmed MW, Alam MN, Rahman MW, Akter F, Basher A, Maude RJ, Faiz MA. Melioidosis in an adult male. Mymensingh Medical Journal 2013; 22(2 ): 413-416. 2026 Ibrahim Medical College. All rights reserved.