Year: 2025
Type: article
Study design: Case Report
Abstract: This report details the case of a 1-year and 11-month-old Filipino female patient who presented with a persistent occipital mass that was soft, non-tender, mobile, and lit through upon transillumination. A neurological test revealed a global developmental delay. Neuroimaging revealed a bony defect at the posterior cranial fossa with herniation of the occipital lobe, cerebrospinal fluid, and the meninges, consistent with Chiari malformation type III, a rare and severe form accounting for less than 1% of Chiari malformations. While this condition typically carries a poor prognosis, the patient showed a favorable outcome following neurosurgical intervention. We present this case to share our clinical experience with this exceedingly rare condition and highlight its potential for positive post-surgical outcomes.
Source: Cureus
DOI: 10.7759/cureus.84482
Institution: José R. Reyes Memorial Medical Center
Language: English
Field: Medicine
Domain: Health Sciences
Open Access status: diamond
OpenAlex ID: W4410539278
