Neuroschistosomiasis: rare CNS infection in a preschool-aged child

Neuroschistosomiasis is a rare but severe manifestation of <i>Schistosoma</i> infection with a challenging diagnosis. We present a paediatric case of neuroschistosomiasis, presenting with persistent vomiting, headache and irritability for seven days. Fundoscopic examination revealed bilateral papilloedema. Brain MRI findings revealed mildly distended sheaths and tortuous optic nerve, suggesting intracranial hypertension. CSF manometry revealed high opening pressure. Schistosomiasis antibodies in blood and CSF were strongly positive. The patient demonstrated an excellent therapeutic response to serial CSF drainage, empirical praziquantel, acetazolamide and corticosteroid treatment. The child gradually improved without neurological sequelae. Prompt diagnosis and treatment are crucial for a favourable outcome and minimising the risk of permanent neurological impairment.

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Publication Details

Journal
BMJ Case Reports
Published
2025-07-01
DOI
https://doi.org/10.1136/bcr-2025-266330
Citations
1
Primary Topic
Parasites and Host Interactions
Type
article
Field-Weighted Citation Impact
2.05
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article

Neuroschistosomiasis: rare CNS infection in a preschool-aged child

Hilal Al-Hashami, Khalid Mohammed, N.K. Panicker, Diyar Hasan Nernji
1 citations
BMJ Case Reports
Parasites and Host Interactions
2.05
article

Neuroschistosomiasis: rare CNS infection in a preschool-aged child

Hilal Al-Hashami, Khalid Mohammed, N.K. Panicker, Diyar Hasan Nernji
article en
1 citations

Abstract

Neuroschistosomiasis is a rare but severe manifestation of <i>Schistosoma</i> infection with a challenging diagnosis. We present a paediatric case of neuroschistosomiasis, presenting with persistent vomiting, headache and irritability for seven days. Fundoscopic examination revealed bilateral papilloedema. Brain MRI findings revealed mildly distended sheaths and tortuous optic nerve, suggesting intracranial hypertension. CSF manometry revealed high opening pressure. Schistosomiasis antibodies in blood and CSF were strongly positive. The patient demonstrated an excellent therapeutic response to serial CSF drainage, empirical praziquantel, acetazolamide and corticosteroid treatment. The child gradually improved without neurological sequelae. Prompt diagnosis and treatment are crucial for a favourable outcome and minimising the risk of permanent neurological impairment.

BMJ Case ReportsVol. 18(7)
Sultan Qaboos Hospital (OM), Royal Hospital (OM)
Good health and well-being
Openalex Percentile: Top 15%
Parasites and Host Interactions
2.05
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