ArticleJournal of neurosurgery. Case lessons2026
A persistent craniopharyngeal canal harboring adenohypophyseal lineages associated with Rathke's cleft cyst: illustrative case.
Article in Journal of neurosurgery. Case lessons, 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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Abstract
backgroundThe craniopharyngeal canal (CPC) is a rare developmental remnant of Rathke's pouch and is occasionally associated with Rathke's cleft cysts (RCCs) and ectopic pituitary tissue. Although embryological and radiological studies have proposed a developmental continuum among these entities, pathological characterization of residual pituitary tissue within CPC remnants in adult patients remains limited. OBSERVATIONS: A 40-year-old woman presented with visual field impairment secondary to suprasellar RCC. Endoscopic endonasal surgery revealed a bony canal extending through the sphenoid sinus from the sellar floor to the posterior pharyngeal wall, consistent with a persistent CPC. Histologically, the canal tissue contained nests of adenohypophyseal cells within a fibromuscular stroma. Immunohistochemical analysis expressed pituitary lineage-specific transcription factors, including PIT-1, with focal SF-1 and T-Pit positivity, which indicate multiple adenohypophyseal lineages. Intraoperative observations of the cystic cavity revealed a dimple-like structure at the corresponding anatomical site. LESSONS: This case demonstrates that pituitary tissue may persist within a type 1 CPC on imaging. Moreover, residual adenohypophyseal cells within the canal can exhibit multiple lineage-specific transcription factor profiles, supporting a spectrum of developmental arrest in Rathke's pouch remnants. https://thejns.org/doi/10.3171/CASE25671.
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