
Also known as craniopharyngioma (disorder), craniopharyngioma (morphologic abnormality), neoplasm of Rathke's Pouch
A craniopharyngioma is a rare type of brain tumor derived from pituitary gland embryonic tissue that occurs most commonly in children, but also affects adults. It may present at any age, even in the prenatal and neonatal periods, but peak incidence rates are childhood-onset at 5–14 years and adult-onset at 50–74 years. People may present with bitemporal inferior quadrantanopia leading to bitemporal hemianopsia, as the tumor may compress the optic chiasm. It has a point prevalence around two per 1,000,000. Craniopharyngiomas are distinct from Rathke's cleft tumours and intrasellar arachnoid cys
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頭蓋咽頭腫とは良性脳腫瘍のひとつで、の3%を占める。胎生期の頭蓋咽頭管が消えずに残ったものから発生した先天性腫瘍と考えられている。全年齢で診断されうるが多くは小児に発生し、小児脳腫瘍の中の約9%(第4位)を占める。発生場所はで、7割がトルコ鞍の中あるいはその直上に存在する。嚢胞を形成しやすく、中にモーター油に似た内用液とコレステロール結晶を含む。腫瘍実質内には、砂状、結節状の石灰沈着がみられる。
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Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).