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Melioidosis/Whitmore’s	Disease		
Fadel	Muhammad	Garishah,	M.D.
Case	1	
A	41-year-old	Indonesian	male	was	referred	from	I	La	Galigo	Hospital,	East	
Luwu	Regency,	to	Wahidin	Hospital	in	August	2012	with	a	5-day	history	of	
fever,	chill,	shortness	of	breath,	headache,	and	confusion.	The	patient	was	an	
exca-	vator	operator	working	in	Tambak	Yoso	village,	Kalaena	District,	East	
Luwu	Regency,	and	had	no	history	of	underlying	diseases.		
On	admission,	the	physical	examination	revealed	fever	(39.8°C),	icteric	sclera,	
hepatomegaly,	abdominal	tenderness,	and	calf	tenderness.	The	blood	test	
results	showed	leukope-	nia	(2,700/μL),	thrombocytopenia	(37,000/μL),	
hyperglycemia	(350	mg/dL),	hyperbilirubinemia	(total	bilirubin	4.4	mg/dL	and	
direct	bilirubin	3.9	mg/dL)	and	hypercreatinemia	(4.5	mg/dL).		
Rapid	diagnostic	tests	for	leptospirosis,	dengue	infection,	and	malaria	were	all	
negative.	He	was	presumptively	diagnosed	as	having	Weil’s	disease	and	type	
2	diabetes	mellitus.	Intravenous	ceftriaxone	and	subcutaneous	insulin	were	
initiated.	He	died	the	following	day	because	of	septic	shock.	His	blood	culture	
became	positive	for	B.	pseudomallei	5	days	after	admission.		
	
	
https://www.ncbi.nlm.nih.gov/pubmed/
26458777
Case	2	
A	45-year-old	Indonesian	female	was	referred	from	Daya	Regional	Hospital,	Makassar,	
to	Wahidin	Hospital	in	July	2013	with	a	3-month	history	of	swelling	on	the	right	side	of	
the	neck.	During	the	past	month,	the	mass	became	bigger,	ruptured,	and	produced	
thick,	white	pus.	She	also	had	fever,	abdominal	pain,	vomiting,	diarrhea	and	poor	
appetite,	and	had	lost	5	kg	during	the	previous	month.	The	patient	was	a	housewife	
living	in	Makassar	and	had	a	3-year	history	of	diabetes	mellitus	and	hypertension.		
On	admission,	she	was	febrile	(38.1°C)	with	a	discharging	neck	abscess	that	was	
swabbed	for	culture.	The	blood	test	results	showed	hyperglycemia	(310	mg/dL),	while	
the	com-	plete	blood	count,	renal	function	tests,	and	liver	function	tests	were	normal.	
Chest	radiography	showed	cardiomegaly	with	pulmonary	edema	and	signs	of	
pulmonary	hypertension.	Her	sputum	examination	was	negative	for	acid-fast	bacilli.	
She	was	diagnosed	as	suspected	tuberculous	lymphadenitis	and	type	2	diabetes	
mellitus.	Intravenous	ceftriaxone,	sub-	cutaneous	insulin,	and	oral	meloxicam	and	
metronidazole	were	initiated.	On	the	4th	day,	she	developed	dyspnea,	and	chronic	
heart	failure	due	to	coronary	artery	disease	was	diagnosed	by	a	cardiologist.	On	the	
6th	day,	she	died	and	her	cause	of	death	was	recorded	as	cardiogenic	shock.	Pus	
culture	was	reported	positive	for	B.	pseudomallei	7	days	after	admission.		
https://www.ncbi.nlm.nih.gov/pubmed/
26458777
Case	3	
A	26-year-old	Indonesian	male	presented	at	Ear	Nose	Throat	(ENT)	
Clinic,	Wahidin	Hospital,	Makassar,	in	Febru-	ary	2014	with	a	10-day	
history	of	an	abscess	behind	his	left	ear	that	was	not	improving	
despite	treatment.	Ten	days	before	presenting	at	the	Wahidin	
hospital,	he	had	noticed	a	painful,	erythematous,	and	immobile	
marble-sized	lump	behind	his	ear.	The	mass	had	been	incised	and	
drained	at	a	private	hospital	in	Makassar	and	he	was	given	an	
unknown	medication.	He	was	an	employee	of	a	State-owned	
enterprise	and	had	no	history	of	underlying	diseases.		
At	the	ENT	clinic,	he	was	afebrile	(36.6°C).	Physical	examination	
revealed	that	his	hearing	was	normal	and	his	tympanic	membrane	was	
intact.	The	incised	wound	was	pain-	less.	The	wound	was	dressed	and	
oral	ciprofloxacin	was	pre-	scribed.	After	8	days,	he	came	back	to	the	
ENT	clinic	complaining	of	a	persistent	discharge.	A	further	incision	and	
drainage	was	performed,	and	the	pus	was	sent	for	bacterial	culture,	
which	was	reported	as	positive	for	B.	pseudomallei	3	days	later.		
	
https://www.ncbi.nlm.nih.gov/pubmed/
26458777
Melioidosis	
•  Burma	1911:	Alfred	Whitmore	(pathologist)	and	his	assisstant	
Krishnaswami	identified	a	new	disease	resembling	glander	(infection	of	
horses)	
•  1932:	Stanton	and	Fletcher	renamed	it	with	melioidosis,	a	Greek	melis	
(donkey’s	health)	and	eidos	(resembling)	
•  Clinically	manifested	as	pneumonia,	multiple	abscesses	and	septicemia		
•  Risk	factors:	working	as	farmer,	drinking	not	boiled	water,	healthcare	
workers	
•  Predispositions:	diabetes,	chronic	kidney	disease,	immunosuppression
Incidence	
•  North	Australia,	Thailand	50	cases/100.000	
population	exceeding	HIV	and	Tuberculosis	
•  Malaysia,	Singapore,	Vietnam,	Cambodia,	and	
Laos	are	also	regions	of	endemic	disease.
Medical	Microbiology:	Burkholderia	pseudomallei	
Gram	Negative;	Aerobic;	Non-Spore	Forming,		
Environmentally-saprophytic	Bacteria	found	in	wet	soil
Global	Distribution	of	Melioidosis	The new engl and jour nal of medicine
VIRULENCE FACTORS
Multiple potential virulence factors have been de-
scribed for B. pseudomallei, but the relative impor-
of the actin cytoskeleton and ultimately to cell
death.16
Highly endemic disease
Endemic disease
Sporadic and possibly
endemic disease
Cluster of endemic disease
Figure 1. Global Distribution of Melioidosis.
Areas where melioidosis is highly endemic, endemic, or sporadic and possibly endemic are indicated. This reflects current knowledge
that is based on limited evidence and is likely to change over time.
Clinical	Manifestations
Port	de	
entree	
Percutaneous	
Inhalation	
Ingestion
Percutaneous	
Inoculation	
Asymptomatic	 Local	Ulcer	 Bacteremia
Ingestion	
Asymptomatic	
GI	tract	Ulceration,	
Lymphadenopathy	
Bacteremia/Severe	
Sepsis	
Bacteremia
Inhalation	
Asymptomatic	 Pneumonia	
Bacteremia/
Severe	Sepsis
Therapy	
Antimicrobial	 IV	(10-14	days),	PO	(3-6	months)	
Ceftazidime	 50	mg/kg	per	6-8	hour	
Meropenem	 25	mg/kg	per	8	hour	
Imipenem	 25	mg/kg	per	8	hour	
TMP/SMX	
>	60	kg	 TMP	320mg/SMX	1600	mg	per	12	Hour	
40-60	kg	 TMP	240mg/SMX	1200mg	per	12	Hour	
<	40	kg	 TMP	160mg/SMX	800mg	per	12	Hour	
<40	kg	 TMP	8mg/kg	/	SMX	40mg/kg	per	12	Hour	
Amoxicillin/Clavulanic	Acid	 Amoxicillin	20m/kg	/	Clavulanic	Acid	5mg/kg	
per	8	hours

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