ArticleCureus2026
Incidentally Detected Colloid Cyst in a Pediatric Patient With Facio-Audio-Symphalangism Syndrome: A Case Report.
Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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3 authors.
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Abstract
Colloid cysts are rare, benign intracranial lesions typically arising from the anterosuperior third ventricle. Although commonly diagnosed in adults, their occurrence in pediatric patients is uncommon and may follow a more aggressive clinical course, occasionally resulting in acute deterioration or sudden death. The association between colloid cysts and genetic syndromes remains poorly understood. We report the case of a nine-year-old girl with facio-audio-symphalangism syndrome in whom a third ventricular colloid cyst was incidentally discovered during routine surveillance imaging. The patient was neurologically stable and asymptomatic with no clinical features of raised intracranial pressure. Neuroimaging revealed a well-circumscribed lesion at the foramen of Monro with imaging characteristics consistent with a colloid cyst measuring 1.2 × 1.0 × 0.8 cm and mild ventricular enlargement. Genetic testing demonstrated a heterozygous mutation in the
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