医学
组织病理学
垂体腺瘤
病态的
垂体瘤
疾病
腺瘤
病理
内科学
作者
Ken K. Y. Ho,Maria Fleseriu,John Wass,Laurence Katznelson,Gérald Raverot,Andrew S. Little,Justo P. Castaño,Martín Reincke,M. Beatriz S. Lopes,Ursula B. Kaiser,Philippe Chanson,Mônica R. Gadelha,Шломо Мелмед
标识
DOI:10.1016/s2213-8587(23)00382-0
摘要
Summary
No comprehensive classification system that guides prognosis and therapy of pituitary adenomas exists. The 2022 WHO histopathology-based classification system can only be applied to lesions that are resected, which represent few clinically significant pituitary adenomas. Many factors independent of histopathology provide mechanistic insight into causation and influence prognosis and treatment of pituitary adenomas. We propose a new approach to guide prognosis and therapy of pituitary adenomas by integrating clinical, genetic, biochemical, radiological, pathological, and molecular information for all adenomas arising from anterior pituitary cell lineages. The system uses an evidence-based scoring of risk factors to yield a cumulative score that reflects disease severity and can be used at the bedside to guide pituitary adenoma management. Once validated in prospective studies, this simple manageable classification system could provide a standardised platform for assessing disease severity, prognosis, and effects of therapy on pituitary adenomas.
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