Skip to main content
Top
Published in: Indian Journal of Pediatrics 1/2019

01-01-2019 | Review Article

Fungal and Parasitic CNS Infections

Authors: Pratibha Singhi, Arushi Gahlot Saini

Published in: Indian Journal of Pediatrics | Issue 1/2019

Login to get access

Abstract

Central nervous system fungal infections can be broadly divided into those that infect a healthy host such as Cryptococcus, Coccidioides, Histoplasma, Blastomyces, Sporothrix spp., and those that cause opportunistic infections in an immunocompromised host such as Candida, Aspergillus, Zygomycetes, Trichosporon spp. The clinical manifestations of central nervous system fungal infections commonly seen in children in clinical practice include a chronic meningitis or meningoencephalitis syndrome, brain abscess, rhino-cerebral syndrome and rarely, a fungal ventriculitis. Fungal central nervous system infections should be suspected in any child with subacute to chronic febrile encephalopathy or meningitis with or without raised intracranial pressure, seizures, orbital pain and/or sero-sanguinous nasal discharge. Diagnosis is corroborated by cerebrospinal fluid analysis, culture and PCR, special stains, serological tests and neuroimaging. Management of fungal central nervous system infections include specific antifungal therapy and supportive measures for associated problems, management of underlying predisposing condition and surgical intervention in cases with localized disease, abscess or presence of simultaneous foreign body such as intracranial shunts. In addition to the fungi, several parasitic infections can cause central nervous system infections in children. Of these, authors briefly discuss cerebral malaria, and amebic meningo-encephalitis.
Literature
1.
go back to reference Redmond A, Dancer C, Woods ML. Fungal infections of the central nervous system: a review of fungal pathogens and treatment. Neurol India. 2007;55:251–9.CrossRefPubMed Redmond A, Dancer C, Woods ML. Fungal infections of the central nervous system: a review of fungal pathogens and treatment. Neurol India. 2007;55:251–9.CrossRefPubMed
2.
go back to reference Singhi P, Nallaswamy K, Singhi S. Fungal infections of the central nervous system. 2nd ed. New York: Oxford University Press; 2016. Singhi P, Nallaswamy K, Singhi S. Fungal infections of the central nervous system. 2nd ed. New York: Oxford University Press; 2016.
3.
go back to reference Singhi S. Fungal infections. 1st ed. London: Mac Keith Press; 2014. Singhi S. Fungal infections. 1st ed. London: Mac Keith Press; 2014.
4.
go back to reference Teive H, Carsten AL, Iwamoto FM, et al. Fungal encephalitis following bone marrow transplantation: clinical findings and prognosis. J Postgrad Med. 2008;54:203–5.CrossRefPubMed Teive H, Carsten AL, Iwamoto FM, et al. Fungal encephalitis following bone marrow transplantation: clinical findings and prognosis. J Postgrad Med. 2008;54:203–5.CrossRefPubMed
5.
go back to reference Zaoutis TE, Roilides E, Chiou CC, et al. Zygomycosis in children: a systematic review and analysis of reported cases. Pediatr Infect Dis J. 2007;26:723–7.CrossRefPubMed Zaoutis TE, Roilides E, Chiou CC, et al. Zygomycosis in children: a systematic review and analysis of reported cases. Pediatr Infect Dis J. 2007;26:723–7.CrossRefPubMed
6.
go back to reference Gumbo T, Chemaly RF, Isada CM, Hall GS, Gordon SM. Late complications of Candida (Torulopsis) glabrata fungemia: description of a phenomenon. Scand J Infect Dis. 2002;34:817–8.CrossRefPubMed Gumbo T, Chemaly RF, Isada CM, Hall GS, Gordon SM. Late complications of Candida (Torulopsis) glabrata fungemia: description of a phenomenon. Scand J Infect Dis. 2002;34:817–8.CrossRefPubMed
7.
go back to reference Likasitwattanakul S, Poneprasert B, Sirisanthana V. Cryptococcosis in HIV-infected children. Southeast Asian J Trop Med Public Health. 2004;35:935–9.PubMed Likasitwattanakul S, Poneprasert B, Sirisanthana V. Cryptococcosis in HIV-infected children. Southeast Asian J Trop Med Public Health. 2004;35:935–9.PubMed
8.
go back to reference Lindsley MD, Mekha N, Baggett HC, et al. Evaluation of a newly developed lateral flow immunoassay for the diagnosis of cryptococcosis. Clin Infect Dis. 2011;53:321–5.CrossRefPubMedPubMedCentral Lindsley MD, Mekha N, Baggett HC, et al. Evaluation of a newly developed lateral flow immunoassay for the diagnosis of cryptococcosis. Clin Infect Dis. 2011;53:321–5.CrossRefPubMedPubMedCentral
9.
go back to reference Horan JL, Perfect JR. Fungal meningitis. 4th ed. Wolters Kluwer Health: Philadelphia; 2014. Horan JL, Perfect JR. Fungal meningitis. 4th ed. Wolters Kluwer Health: Philadelphia; 2014.
10.
go back to reference Jain KK, Mittal SK, Kumar S, Gupta RK. Imaging features of central nervous system fungal infections. Neurol India. 2007;55:241–50.CrossRefPubMed Jain KK, Mittal SK, Kumar S, Gupta RK. Imaging features of central nervous system fungal infections. Neurol India. 2007;55:241–50.CrossRefPubMed
11.
go back to reference Pappas PG, Kauffman CA, Andes D, et al. Clinical practice guidelines for the management of candidiasis: 2009 update by the Infectious Diseases Society of America. Clin Infect Dis. 2009;48:503–35.CrossRefPubMed Pappas PG, Kauffman CA, Andes D, et al. Clinical practice guidelines for the management of candidiasis: 2009 update by the Infectious Diseases Society of America. Clin Infect Dis. 2009;48:503–35.CrossRefPubMed
12.
go back to reference Perfect JR, Dismukes WE, Dromer F, et al. Clinical practice guidelines for the management of cryptococcal disease: 2010 update by the Infectious Diseases Society of America. Clin Infect Dis. 2010;50:291–322.CrossRefPubMedPubMedCentral Perfect JR, Dismukes WE, Dromer F, et al. Clinical practice guidelines for the management of cryptococcal disease: 2010 update by the Infectious Diseases Society of America. Clin Infect Dis. 2010;50:291–322.CrossRefPubMedPubMedCentral
13.
go back to reference Spellberg B, Walsh TJ, Kontoyiannis DP, Edwards J Jr, Ibrahim AS. Recent advances in the management of mucormycosis: from bench to bedside. Clin Infect Dis. 2009;48:1743–51.CrossRefPubMedPubMedCentral Spellberg B, Walsh TJ, Kontoyiannis DP, Edwards J Jr, Ibrahim AS. Recent advances in the management of mucormycosis: from bench to bedside. Clin Infect Dis. 2009;48:1743–51.CrossRefPubMedPubMedCentral
14.
go back to reference Postels DG, Taylor TE. Cerebral malaria. 4th ed. Philadelphia: Wolters Kluwer Health; 2014. Postels DG, Taylor TE. Cerebral malaria. 4th ed. Philadelphia: Wolters Kluwer Health; 2014.
16.
go back to reference Clark IA, Rockett KA. Sequestration, cytokines, and malaria pathology. Int J Parasitol. 1994;24:165–6.CrossRefPubMed Clark IA, Rockett KA. Sequestration, cytokines, and malaria pathology. Int J Parasitol. 1994;24:165–6.CrossRefPubMed
18.
19.
go back to reference Wassmer SC, Moxon CA, Taylor T, Grau GE, Molyneux ME, Craig AG. Vascular endothelial cells cultured from patients with cerebral or uncomplicated malaria exhibit differential reactivity to TNF. Cell Microbiol. 2011;13:198–209.CrossRefPubMedPubMedCentral Wassmer SC, Moxon CA, Taylor T, Grau GE, Molyneux ME, Craig AG. Vascular endothelial cells cultured from patients with cerebral or uncomplicated malaria exhibit differential reactivity to TNF. Cell Microbiol. 2011;13:198–209.CrossRefPubMedPubMedCentral
22.
go back to reference Taylor TE, Fu WJ, Carr RA, et al. Differentiating the pathologies of cerebral malaria by postmortem parasite counts. Nat Med. 2004;10:143–5.CrossRefPubMed Taylor TE, Fu WJ, Carr RA, et al. Differentiating the pathologies of cerebral malaria by postmortem parasite counts. Nat Med. 2004;10:143–5.CrossRefPubMed
23.
go back to reference Kariuki SM, Gitau E, Gwer S, et al. Value of plasmodium falciparum histidine-rich protein 2 level and malaria retinopathy in distinguishing cerebral malaria from other acute encephalopathies in Kenyan children. J Infect Dis. 2014;209:600–9.CrossRefPubMed Kariuki SM, Gitau E, Gwer S, et al. Value of plasmodium falciparum histidine-rich protein 2 level and malaria retinopathy in distinguishing cerebral malaria from other acute encephalopathies in Kenyan children. J Infect Dis. 2014;209:600–9.CrossRefPubMed
24.
go back to reference White NJ, Pukrittayakamee S, Hien TT, Faiz MA, Mokuolu OA, Dondorp AM. Malaria. Lancet. 2014;383:723–35.CrossRefPubMed White NJ, Pukrittayakamee S, Hien TT, Faiz MA, Mokuolu OA, Dondorp AM. Malaria. Lancet. 2014;383:723–35.CrossRefPubMed
25.
go back to reference Jones KL, Donegan S, Lalloo DG. Artesunate versus quinine for treating severe malaria. Cochrane Database Syst Rev. 2007:CD005967. Jones KL, Donegan S, Lalloo DG. Artesunate versus quinine for treating severe malaria. Cochrane Database Syst Rev. 2007:CD005967.
26.
go back to reference Shoff ME, Rogerson A, Kessler K, Schatz S, Seal DV. Prevalence of Acanthamoeba and other naked amoebae in South Florida domestic water. J Water Health. 2008;6:99–104.CrossRefPubMed Shoff ME, Rogerson A, Kessler K, Schatz S, Seal DV. Prevalence of Acanthamoeba and other naked amoebae in South Florida domestic water. J Water Health. 2008;6:99–104.CrossRefPubMed
27.
go back to reference Visvesvara G, Maguire J. Pathogenic and opportunistic free-living amebas. Acanthamoeba spp., Balamuthia mandrillaris, Naegleria fowleri, and Sappinia diploidea. Philadelphia: Churchill Livingstone; 2006. p. 1114–25. Visvesvara G, Maguire J. Pathogenic and opportunistic free-living amebas. Acanthamoeba spp., Balamuthia mandrillaris, Naegleria fowleri, and Sappinia diploidea. Philadelphia: Churchill Livingstone; 2006. p. 1114–25.
28.
go back to reference Visvesvara GS, Booton GC, Kelley DJ, et al. In vitro culture, serologic and molecular analysis of Acanthamoeba isolated from the liver of a keel-billed toucan (Ramphastos sulfuratus). Vet Parasitol. 2007;143:74–8.CrossRefPubMed Visvesvara GS, Booton GC, Kelley DJ, et al. In vitro culture, serologic and molecular analysis of Acanthamoeba isolated from the liver of a keel-billed toucan (Ramphastos sulfuratus). Vet Parasitol. 2007;143:74–8.CrossRefPubMed
29.
go back to reference Gelman BB, Rauf SJ, Nader R, et al. Amoebic encephalitis due to Sappinia diploidea. JAMA. 2001;285:2450–1.CrossRefPubMed Gelman BB, Rauf SJ, Nader R, et al. Amoebic encephalitis due to Sappinia diploidea. JAMA. 2001;285:2450–1.CrossRefPubMed
30.
go back to reference Visvesvara GS, Moura H, Schuster FL. Pathogenic and opportunistic free-living amoebae: Acanthamoeba spp., Balamuthia mandrillaris, Naegleria fowleri, and Sappinia diploidea. FEMS Immunol Med Microbiol. 2007;50:1–26.CrossRefPubMed Visvesvara GS, Moura H, Schuster FL. Pathogenic and opportunistic free-living amoebae: Acanthamoeba spp., Balamuthia mandrillaris, Naegleria fowleri, and Sappinia diploidea. FEMS Immunol Med Microbiol. 2007;50:1–26.CrossRefPubMed
31.
go back to reference Singh P, Kochhar R, Vashishta RK, et al. Amebic meningoencephalitis: spectrum of imaging findings. Am J Neuroradiol. 2006;27:1217–21.PubMed Singh P, Kochhar R, Vashishta RK, et al. Amebic meningoencephalitis: spectrum of imaging findings. Am J Neuroradiol. 2006;27:1217–21.PubMed
32.
go back to reference Qvarnstrom Y, Visvesvara GS, Sriram R, da Silva AJ. Multiplex real-time PCR assay for simultaneous detection of Acanthamoeba spp., Balamuthia mandrillaris, and Naegleria fowleri. J Clin Microbiol. 2006;44:3589–95.CrossRefPubMedPubMedCentral Qvarnstrom Y, Visvesvara GS, Sriram R, da Silva AJ. Multiplex real-time PCR assay for simultaneous detection of Acanthamoeba spp., Balamuthia mandrillaris, and Naegleria fowleri. J Clin Microbiol. 2006;44:3589–95.CrossRefPubMedPubMedCentral
33.
go back to reference Martinez AJ, Visvesvara GS. Free-living, amphizoic and opportunistic amebas. Brain Pathol. 1997;7:583–98.CrossRefPubMed Martinez AJ, Visvesvara GS. Free-living, amphizoic and opportunistic amebas. Brain Pathol. 1997;7:583–98.CrossRefPubMed
34.
go back to reference Tunkel AR, Glaser CA, Bloch KC, et al. The management of encephalitis: clinical practice guidelines by the Infectious Diseases Society of America. Clin Infect Dis. 2008;47:303–27.CrossRefPubMed Tunkel AR, Glaser CA, Bloch KC, et al. The management of encephalitis: clinical practice guidelines by the Infectious Diseases Society of America. Clin Infect Dis. 2008;47:303–27.CrossRefPubMed
35.
go back to reference Poungvarin N, Jariya P. The fifth nonlethal case of primary amoebic meningoencephalitis. J Med Assoc Thailand. 1991;74:112–5. Poungvarin N, Jariya P. The fifth nonlethal case of primary amoebic meningoencephalitis. J Med Assoc Thailand. 1991;74:112–5.
Metadata
Title
Fungal and Parasitic CNS Infections
Authors
Pratibha Singhi
Arushi Gahlot Saini
Publication date
01-01-2019
Publisher
Springer India
Published in
Indian Journal of Pediatrics / Issue 1/2019
Print ISSN: 0019-5456
Electronic ISSN: 0973-7693
DOI
https://doi.org/10.1007/s12098-017-2487-x

Other articles of this Issue 1/2019

Indian Journal of Pediatrics 1/2019 Go to the issue