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Hydrocephalus in Mexican children with Coccidioidal Meningitis: Clinical, serological, and neuroimaging findings

BACKGROUND: Coccidioidal meningitis (CM) is a fungal infectious disease that rarely affects children. Even in endemic areas, coccidiomycosis rarely affects the pediatric population. However, 40% of affected children develop hydrocephalus. Here, we describe the clinical, serological, and neuroimaging...

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Autores principales: De la Cerda-Vargas, María F., Sandoval-Bonilla, B. A., McCarty, James M., De León, Fernando Chico-Ponce, Candelas-Rangel, José A., Rodríguez-Rodríguez, Jorge D., Navarro-Domínguez, Pedro, Muñoz- Hernández, Melisa A., Meza-Mata, Elizabeth, Fernández-González, Elena M., Sámano-Aviña, Mariana G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8053472/
https://www.ncbi.nlm.nih.gov/pubmed/33880224
http://dx.doi.org/10.25259/SNI_895_2020
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author De la Cerda-Vargas, María F.
Sandoval-Bonilla, B. A.
McCarty, James M.
De León, Fernando Chico-Ponce
Candelas-Rangel, José A.
Rodríguez-Rodríguez, Jorge D.
Navarro-Domínguez, Pedro
Muñoz- Hernández, Melisa A.
Meza-Mata, Elizabeth
Fernández-González, Elena M.
Sámano-Aviña, Mariana G.
author_facet De la Cerda-Vargas, María F.
Sandoval-Bonilla, B. A.
McCarty, James M.
De León, Fernando Chico-Ponce
Candelas-Rangel, José A.
Rodríguez-Rodríguez, Jorge D.
Navarro-Domínguez, Pedro
Muñoz- Hernández, Melisa A.
Meza-Mata, Elizabeth
Fernández-González, Elena M.
Sámano-Aviña, Mariana G.
author_sort De la Cerda-Vargas, María F.
collection PubMed
description BACKGROUND: Coccidioidal meningitis (CM) is a fungal infectious disease that rarely affects children. Even in endemic areas, coccidiomycosis rarely affects the pediatric population. However, 40% of affected children develop hydrocephalus. Here, we describe the clinical, serological, and neuroimaging findings in a series of Mexican children admitted to our neurosurgical service with hydrocephalus and subsequently diagnosed with CM. METHODS: We report a prospective series of pediatric patients with hydrocephalus secondary to CM in an endemic area at the north of Mexico. Our report includes children with CM who were hospitalized from 2015 to 2019 in a regional hospital in Torreón, Coahuila. Clinical evolution was monitored for 1 year after hospital discharge. RESULTS: Our series include five children with CM (2–17-years-old, three female), who were hospitalized for hydrocephalus and developed intracranial hypertension. The most frequent neuroimaging findings were leptomeningeal enhancement (5/5) and basal arachnoiditis (4/5), followed by asymmetric hydrocephalus (3/5), abnormalities in fourth ventricle morphology (3/5), and cerebral vasculitis (2/5). CM was diagnosed by positive serology or pathology studies. All children were initially managed with fluconazole and a shunt was placed for management of hydrocephalus. Four patients recovered without permanent neurological deficits and one subject developed persistent vegetative state. One year after hospital discharge, none of the subjects died. CONCLUSION: This series contributes to the limited number of pediatric CM cases reported in the literature, and describes neuroimaging findings in the pediatric population. The cases here presented show that the identification of Coccidioides as causal agent in pediatric meningitis is crucial for targeted treatment and can affect dramatically neurological prognosis. Furthermore, our report stresses that even in endemic areas pediatric coccidiomycosis represents a diagnostic challenge, which is further exacerbated by the limited availability of resources in these regions. Therefore, a positive immunoglobulin G by enzyme immunoassay is enough for diagnosis of CM in endemic areas without access to CF.
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spelling pubmed-80534722021-04-19 Hydrocephalus in Mexican children with Coccidioidal Meningitis: Clinical, serological, and neuroimaging findings De la Cerda-Vargas, María F. Sandoval-Bonilla, B. A. McCarty, James M. De León, Fernando Chico-Ponce Candelas-Rangel, José A. Rodríguez-Rodríguez, Jorge D. Navarro-Domínguez, Pedro Muñoz- Hernández, Melisa A. Meza-Mata, Elizabeth Fernández-González, Elena M. Sámano-Aviña, Mariana G. Surg Neurol Int Case Report BACKGROUND: Coccidioidal meningitis (CM) is a fungal infectious disease that rarely affects children. Even in endemic areas, coccidiomycosis rarely affects the pediatric population. However, 40% of affected children develop hydrocephalus. Here, we describe the clinical, serological, and neuroimaging findings in a series of Mexican children admitted to our neurosurgical service with hydrocephalus and subsequently diagnosed with CM. METHODS: We report a prospective series of pediatric patients with hydrocephalus secondary to CM in an endemic area at the north of Mexico. Our report includes children with CM who were hospitalized from 2015 to 2019 in a regional hospital in Torreón, Coahuila. Clinical evolution was monitored for 1 year after hospital discharge. RESULTS: Our series include five children with CM (2–17-years-old, three female), who were hospitalized for hydrocephalus and developed intracranial hypertension. The most frequent neuroimaging findings were leptomeningeal enhancement (5/5) and basal arachnoiditis (4/5), followed by asymmetric hydrocephalus (3/5), abnormalities in fourth ventricle morphology (3/5), and cerebral vasculitis (2/5). CM was diagnosed by positive serology or pathology studies. All children were initially managed with fluconazole and a shunt was placed for management of hydrocephalus. Four patients recovered without permanent neurological deficits and one subject developed persistent vegetative state. One year after hospital discharge, none of the subjects died. CONCLUSION: This series contributes to the limited number of pediatric CM cases reported in the literature, and describes neuroimaging findings in the pediatric population. The cases here presented show that the identification of Coccidioides as causal agent in pediatric meningitis is crucial for targeted treatment and can affect dramatically neurological prognosis. Furthermore, our report stresses that even in endemic areas pediatric coccidiomycosis represents a diagnostic challenge, which is further exacerbated by the limited availability of resources in these regions. Therefore, a positive immunoglobulin G by enzyme immunoassay is enough for diagnosis of CM in endemic areas without access to CF. Scientific Scholar 2021-03-24 /pmc/articles/PMC8053472/ /pubmed/33880224 http://dx.doi.org/10.25259/SNI_895_2020 Text en Copyright: © 2021 Surgical Neurology International https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
De la Cerda-Vargas, María F.
Sandoval-Bonilla, B. A.
McCarty, James M.
De León, Fernando Chico-Ponce
Candelas-Rangel, José A.
Rodríguez-Rodríguez, Jorge D.
Navarro-Domínguez, Pedro
Muñoz- Hernández, Melisa A.
Meza-Mata, Elizabeth
Fernández-González, Elena M.
Sámano-Aviña, Mariana G.
Hydrocephalus in Mexican children with Coccidioidal Meningitis: Clinical, serological, and neuroimaging findings
title Hydrocephalus in Mexican children with Coccidioidal Meningitis: Clinical, serological, and neuroimaging findings
title_full Hydrocephalus in Mexican children with Coccidioidal Meningitis: Clinical, serological, and neuroimaging findings
title_fullStr Hydrocephalus in Mexican children with Coccidioidal Meningitis: Clinical, serological, and neuroimaging findings
title_full_unstemmed Hydrocephalus in Mexican children with Coccidioidal Meningitis: Clinical, serological, and neuroimaging findings
title_short Hydrocephalus in Mexican children with Coccidioidal Meningitis: Clinical, serological, and neuroimaging findings
title_sort hydrocephalus in mexican children with coccidioidal meningitis: clinical, serological, and neuroimaging findings
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8053472/
https://www.ncbi.nlm.nih.gov/pubmed/33880224
http://dx.doi.org/10.25259/SNI_895_2020
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