Case Report: Granulomatous Amebic Encephalitis due to Acanthamoeba spp. in an Immunocompetent Pediatric Patient
Author(s) -
Denisse Vaquera Aparicio,
José Iván Castillo Bejarano,
Abiel Mascareñas de los Santos,
Sergio Ramírez-Cortinas,
Manuel Enrique de la O-Cavazos
Publication year - 2021
Publication title -
american journal of tropical medicine and hygiene
Language(s) - English
Resource type - Journals
eISSN - 1476-1645
pISSN - 0002-9637
DOI - 10.4269/ajtmh.21-0129
Subject(s) - medicine , headaches , encephalitis , vomiting , magnetic resonance imaging , pediatrics , acanthamoeba , rare disease , disease , pathology , surgery , immunology , radiology , virus , biology , microbiology and biotechnology
. Granulomatous amebic encephalitis (GAE) caused by Acanthamoeba is a rare infection with central nervous system (CNS) involvement usually with fatal consequences. Currently, information regarding GAE in children is scarce and is limited only to case reports and case series. A 13-year-old immunocompetent male patient with a 6-month history of progressive and intermittent headaches presented to our institution. One week before hospital admission, the patient showed signs of CNS involvement. Magnetic resonance imaging revealed multiple lesions with supra- and infratentorial cerebral abscesses. An empiric treatment with combined antibiotics was given, but the patient died after 20 days of hospital stay. A postmortem diagnosis confirmed GAE. Although it is a rare disease in pediatric patients, GAE should be considered in children with a chronic history of fever, headache, and vomiting with CNS involvement.
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