Parenchymal neurocysticercosis complicated by hydrocephalus: A rare case report with mechanistic insights.

Parasitol IntJun 4, 2026 (epub)

Xinghua Tie, Liping Zhang

✦ AI-curated · Sources linked

Case in brief

A 45-year-old male presented with a 20-year history of cognitive decline, gait instability, urinary incontinence, and recurrent seizures. Neuroimaging revealed multiple parenchymal cysticercal lesions causing impaired cerebrospinal fluid circulation and hydrocephalus. The patient underwent ventriculoperitoneal shunting along with albendazole therapy and antiepileptic treatment, resulting in significant symptomatic improvement and seizure-free survival at one-year follow-up.

What made this case unusual

This case highlights the rare association of parenchymal neurocysticercosis with hydrocephalus due to the formation of a cerebral aqueductal septum, which is not commonly reported.

Diagnostic / clinical pearl

Clinicians should consider neurocysticercosis in patients with progressive neurological symptoms and a relevant epidemiological history, especially in endemic regions.

Why it matters

Understanding the mechanisms of hydrocephalus in neurocysticercosis can guide effective management strategies and improve patient outcomes in similar cases.

Source

Published in Parasitol Int. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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