原发性醛固酮增多症
组织病理学
医学
亚临床感染
病理
醛固酮增多症
醛固酮
组织学
生物信息学
继发性高血压
小学(天文学)
仿形(计算机编程)
病理生理学
基因表达谱
旁分泌信号
体细胞
内科学
醛固酮合酶
纤维化
磁共振成像
神经科学
作者
Yingxian Pang,Zhuolun Sun,Tracy Ann Williams
出处
期刊:Hypertension
[Lippincott Williams & Wilkins]
日期:2026-03-30
卷期号:83 (5): e26225-e26225
标识
DOI:10.1161/hypertensionaha.126.26225
摘要
Primary aldosteronism is the most common surgically treatable form of hypertension. Surgically amenable forms are characterized by lateralized aldosterone overproduction, which may occur along a spectrum ranging from true unilateral hypersecretion to asymmetrical bilateral production. Historically attributed to solitary aldosterone-producing adenomas, lateralized primary aldosteronism is now recognized to encompass a range of histopathologic lesions, including aldosterone-producing micronodules, reflecting a continuum from subclinical autonomous secretion to overt primary aldosteronism. This review synthesizes recent evidence demonstrating how histopathology, genetics, and cellular mapping can collectively explain some of the heterogeneity in surgical outcomes. The Histopathology of Primary Aldosteronism consensus classifies lateralized primary aldosteronism into classical (aldosterone-producing adenoma-predominant) and nonclassical (aldosterone-producing micronodule-predominant) forms, with the former linked to biochemical remission and the latter associated with persistent or recurrent aldosteronism. Somatic driver mutations further correlate with histology and outcomes, while single-cell and spatial omics data reveal distinct pathogenic trajectories and metabolic profiles underlying tumor progression. Together, these advances offer a more precise, pathophysiology-based framework to improve diagnosis, subtyping, and outcome prediction, advancing tailored management for this disease.
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