文章：

垂体及异位促肾上腺皮质激素分泌肿瘤的转录组全分析

Transcriptome-Wide Analysis of Pituitary and Ectopic Adrenocorticotropic Hormone-Secreting Tumors

原文发布日期：15 February 2025

DOI: 10.3390/cancers17040658

类型: Article

开放获取: 是

英文摘要：

Endogenous Cushing’s syndrome (CS) is a rare neuroendocrine disorder characterized by either secondary cortisol increases due to an adrenocorticotropic hormone (ACTH)-secreting pituitary tumor (Cushing’s disease (CD)), an ACTH-secreting neuroendocrine tumor (NET) of non-pituitary origin (ectopic ACTH syndrome (EAS)), or by the primarily adrenal autonomous overproduction of cortisol [...]

摘要翻译： 

内源性库欣综合征（CS）是一种罕见的神经内分泌疾病，其特征可表现为以下三种病理类型：由分泌促肾上腺皮质激素（ACTH）的垂体肿瘤引起的继发性皮质醇增多症（即库欣病（CD））；由非垂体来源的分泌ACTH的神经内分泌肿瘤（NET）导致的异位ACTH综合征（EAS）；或由肾上腺自主性皮质醇过度分泌[...]

原文链接：

Transcriptome-Wide Analysis of Pituitary and Ectopic Adrenocorticotropic Hormone-Secreting Tumors