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==Overview==
==Overview==


'''Granulomatous amoebic encephalitis''' is a [[central nervous system]] disease caused by certain species of [[amoeba]], especially ''[[Balamuthia mandrillaris]]''.
'''Granulomatous amoebic encephalitis''' is a [[central nervous system]] disease caused by certain species of [[amoeba]], especially ''[[Balamuthia mandrillaris]]''.<ref name="pmid15211011">{{cite journal |author=Intalapaporn P, Suankratay C, Shuangshoti S, Phantumchinda K, Keelawat S, Wilde H |title=Balamuthia mandrillaris meningoencephalitis: the first case in southeast Asia |journal=[[The American Journal of Tropical Medicine and Hygiene]] |volume=70 |issue=6 |pages=666–9 |year=2004 |month=June |pmid=15211011 |doi= |url=}}</ref>
 
==Pathophysiology==
 
Granulomatous amoebic encephalitis is most commonly caused by Acanthamoeba castellanii, A. culbertsoni, A. polyphaga or [[Balamuthia mandrillaris]].<ref>Martinez AJ, Visvesvara GS, Chandler FW. Free-living amebic infections. Chapter 132 in Pathology of Infectious Diseases, 1997, Connor DH, Chandler FW, Manz HJ, Schwartz DA, Lack EE, eds., Stamford, Appleton & Lange, pp 1163-1176.</ref> It is rarely due to [[Entamoeba histolytica]].
 
==Epidemiology and Demographics==
 
Balamuthia infection is very rare but often causes fatal disease[1]. Since Balamuthia was first discovered in 1986, about 200 cases of infection have been reported worldwide[2,3,4]. This number includes at least 70 confirmed cases in the United States.
 
==Risk Factors==
 
The Balamuthia amoeba is able to infect  anyone, including healthy people[1-6]. Those at increased risk for infection[1-4,6,10] include people with [[HIV]]/[[AIDS]], [[cancer]], liver disease, or  [[diabetes mellitus]], people taking immune system inhibiting drugs, [[Alcoholism|alcoholics]], young  children or the elderly and [[pregnancy|pregnant women.]]<ref name="pmid15211011">{{cite journal |author=Intalapaporn P, Suankratay C, Shuangshoti S, Phantumchinda K, Keelawat S, Wilde H |title=Balamuthia mandrillaris meningoencephalitis: the first case in southeast Asia |journal=[[The American Journal of Tropical Medicine and Hygiene]] |volume=70 |issue=6 |pages=666–9 |year=2004 |month=June |pmid=15211011 |doi= |url=}}</ref>.
 
==Causes==
 
Balamuthia mandrillaris has only recently been isolated from the environment and has also been isolated from autopsy specimens of infected humans and animals. B. mandrillaris has only two stages, [[cyst]]s  and [[trophozoites]] , in its life cycle. No flagellated stage exists as part of the life cycle. The [[trophozoites]] replicate by [[mitosis]] (nuclear membrane does not remain intact) . The trophozoites are the infective forms, although both [[cyst]]s and [[trophozoites]] gain entry into the body  through various means. Entry can occur through the nasal passages to the lower respiratory tract , or ulcerated or broken skin . When B. mandrillaris enters the respiratory system or through the [[skin]], it can invade the [[central nervous system]] by hematogenous dissemination causing [[granulomatous amebic encephalitis]] (GAE)  or disseminated disease , or skin lesions  in individuals who are immune competent as well as those with compromised immune systems. B. mandrillaris [[cyst]]s and [[trophozoites]] are found in tissue.
 
==Diagnosis==
===History and Symptoms===
 
Balamuthia infection is very rare. The Balamuthia amebas can infect the skin, sinuses, brain and other organs of the body. Therefore, Balamuthia infection can cause a wide range of symptoms. Disease  can begin with a skin wound on the face, trunk, or limbs and can then progress  to the brain where it cause a disease called Granulomatous Amebic Encephalitis
 
===Laboratory Findings===
 
The [[indirect immunofluorescence assay]] (IFA) is a test used to detect antibodies attached to Balamuthia amebas in body tissues. In contrast, [[immunohistochemistry]] (IHC) uses specific antibodies against Balamuthia to detect the amoebas. Finally, a [[polymerase chain reaction]] (PCR) molecular assay can detect Balamuthia DNA.
 
===MRI===
 
[[Magnetic resonance imaging]] (MRI) scans may show increased signal on T2-weighted images. The lesions may show ring enhancement with intravenous contrast studies. Occasionally, there are neuro-radiographic findings of an expanding intracranial mass that may mimic a cerebral tumor or a [[brain abscess]].
 
===CT===
 
A [[computerized tomography]] scan may demonstrate bilateral low-density areas with mild mass effect in the cortex and subcortical white matter.
 
==Treatment==
===Medical Therapy===
 
GAE can, in general, must be treated by killing the pathogenic amoebas which cause it. Even with treatment, the condition is often fatal, and there are very few recorded survivors, almost all of whom suffered permanent [[neurocognitive|neurocognitive deficits]]. Several drugs have been shown to be effective against GAE-causing organisms ''[[in vitro]]''.<ref>http://path.upmc.edu/cases/case156/dx.html</ref>
 
===Primary Prevention===
 
Currently, there are no known ways to prevent infection with Balamuthia since it is unclear how and why some people become infected while others do not.
There have been no reports of a Balamuthia infection spreading from one person  to another except through organ donation/transplantation.


==References==
==References==
{{Reflist|2}}
{{Reflist|2}}
[[Category:Disease]]
[[Category:Neurology]]


==External links==
* {{cite journal |author=Intalapaporn P, Suankratay C, Shuangshoti S, Phantumchinda K, Keelawat S, Wilde H |title=Balamuthia mandrillaris meningoencephalitis: the first case in southeast Asia |journal=Am. J. Trop. Med. Hyg. |volume=70 |issue=6 |pages=666-9 |year=2004 |pmid=15211011 |url=http://www.ajtmh.org/cgi/content/full/70/6/666}}
[[Category:Neurology]]
[[Category:Infectious disease]]


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Latest revision as of 17:50, 18 September 2017

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Granulomatous amoebic encephalitis is a central nervous system disease caused by certain species of amoeba, especially Balamuthia mandrillaris.[1]

Pathophysiology

Granulomatous amoebic encephalitis is most commonly caused by Acanthamoeba castellanii, A. culbertsoni, A. polyphaga or Balamuthia mandrillaris.[2] It is rarely due to Entamoeba histolytica.

Epidemiology and Demographics

Balamuthia infection is very rare but often causes fatal disease[1]. Since Balamuthia was first discovered in 1986, about 200 cases of infection have been reported worldwide[2,3,4]. This number includes at least 70 confirmed cases in the United States.

Risk Factors

The Balamuthia amoeba is able to infect anyone, including healthy people[1-6]. Those at increased risk for infection[1-4,6,10] include people with HIV/AIDS, cancer, liver disease, or diabetes mellitus, people taking immune system inhibiting drugs, alcoholics, young children or the elderly and pregnant women.[1].

Causes

Balamuthia mandrillaris has only recently been isolated from the environment and has also been isolated from autopsy specimens of infected humans and animals. B. mandrillaris has only two stages, cysts and trophozoites , in its life cycle. No flagellated stage exists as part of the life cycle. The trophozoites replicate by mitosis (nuclear membrane does not remain intact) . The trophozoites are the infective forms, although both cysts and trophozoites gain entry into the body through various means. Entry can occur through the nasal passages to the lower respiratory tract , or ulcerated or broken skin . When B. mandrillaris enters the respiratory system or through the skin, it can invade the central nervous system by hematogenous dissemination causing granulomatous amebic encephalitis (GAE) or disseminated disease , or skin lesions in individuals who are immune competent as well as those with compromised immune systems. B. mandrillaris cysts and trophozoites are found in tissue.

Diagnosis

History and Symptoms

Balamuthia infection is very rare. The Balamuthia amebas can infect the skin, sinuses, brain and other organs of the body. Therefore, Balamuthia infection can cause a wide range of symptoms. Disease can begin with a skin wound on the face, trunk, or limbs and can then progress to the brain where it cause a disease called Granulomatous Amebic Encephalitis

Laboratory Findings

The indirect immunofluorescence assay (IFA) is a test used to detect antibodies attached to Balamuthia amebas in body tissues. In contrast, immunohistochemistry (IHC) uses specific antibodies against Balamuthia to detect the amoebas. Finally, a polymerase chain reaction (PCR) molecular assay can detect Balamuthia DNA.

MRI

Magnetic resonance imaging (MRI) scans may show increased signal on T2-weighted images. The lesions may show ring enhancement with intravenous contrast studies. Occasionally, there are neuro-radiographic findings of an expanding intracranial mass that may mimic a cerebral tumor or a brain abscess.

CT

A computerized tomography scan may demonstrate bilateral low-density areas with mild mass effect in the cortex and subcortical white matter.

Treatment

Medical Therapy

GAE can, in general, must be treated by killing the pathogenic amoebas which cause it. Even with treatment, the condition is often fatal, and there are very few recorded survivors, almost all of whom suffered permanent neurocognitive deficits. Several drugs have been shown to be effective against GAE-causing organisms in vitro.[3]

Primary Prevention

Currently, there are no known ways to prevent infection with Balamuthia since it is unclear how and why some people become infected while others do not. There have been no reports of a Balamuthia infection spreading from one person to another except through organ donation/transplantation.

References

  1. 1.0 1.1 Intalapaporn P, Suankratay C, Shuangshoti S, Phantumchinda K, Keelawat S, Wilde H (2004). "Balamuthia mandrillaris meningoencephalitis: the first case in southeast Asia". The American Journal of Tropical Medicine and Hygiene. 70 (6): 666–9. PMID 15211011. Unknown parameter |month= ignored (help)
  2. Martinez AJ, Visvesvara GS, Chandler FW. Free-living amebic infections. Chapter 132 in Pathology of Infectious Diseases, 1997, Connor DH, Chandler FW, Manz HJ, Schwartz DA, Lack EE, eds., Stamford, Appleton & Lange, pp 1163-1176.
  3. http://path.upmc.edu/cases/case156/dx.html


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