ArticleJCEM case reports2026
Papillary craniopharyngioma following an initial diagnosis of Rathke cleft cyst: a case report and narrative review.
Article in JCEM case reports, 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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4 authors.
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Abstract
A 59-year-old man presented with a giant suprasellar cystic lesion causing obstructive hydrocephalus. Radiological and intraoperative findings suggested a cystic craniopharyngioma (CP); however, histopathology was interpreted as most consistent with a Rathke cleft cyst (RCC). Six years later, surveillance imaging demonstrated recurrence as a new mixed solid-cystic suprasellar mass with infundibular thickening. Histopathology showed papillary architecture with diffuse
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