Tortora Fabio, Negro Alberto, Briganti Francesco, Del Basso De Caro Maria Laura, Cavallo Luigi Maria, Solari Domenico, Somma Teresa, Brunese Luca, Caranci Ferdinando
Unit of Interventional Neuroradiology, Department of Advanced Biomedical Sciences, "Federico II" University, Naples, Italy.
Neuroradiology Unit, Ospedale del Mare, Naples, Italy.
Gland Surg. 2020 Dec;9(6):2260-2268. doi: 10.21037/gs-20-654.
Cushing's syndrome is a pathological clinical condition caused by an exposure of elevated cortisol levels over a long period of time. It is therefore essential to establish what the cause of hypercortisolism is. In most cases (about 80%) the pathological process is due to adrenocorticotropic hormone (ACTH), while in a minor part of the cases (about 20%) the cause is represented by a pathology of the adrenal glands and therefore not related to ACTH. Most patients with ACTH dependent Cushing's syndrome have a pituitary microadenoma; in the remaining cases (30%), the high level of cortisol is linked to an ectopic secretion of ACTH. Surgical removal of the pituitary adenoma represents the treatment of choice in Cushing's disease (CD) patients; it is therefore necessary to identify and precisely locate the pituitary tumour responsible for the secretion of ACTH. Adequate diagnostic information is very often, even with magnetic resonance imaging (MRI), and in these cases we rely on bilateral inferior petrosal sinuses sampling (BIPSS). This procedure is considered the gold standard method for the diagnosis, but like any other diagnostic method it is not free from erroneous results such as false positives or false negatives.
库欣综合征是一种由于长期暴露于高水平皮质醇而导致的病理性临床病症。因此,确定高皮质醇血症的病因至关重要。在大多数情况下(约80%),病理过程是由促肾上腺皮质激素(ACTH)引起的,而在少数情况下(约20%),病因是肾上腺的病变,因此与ACTH无关。大多数依赖ACTH的库欣综合征患者患有垂体微腺瘤;在其余病例(30%)中,皮质醇水平升高与ACTH的异位分泌有关。手术切除垂体腺瘤是库欣病(CD)患者的首选治疗方法;因此,有必要识别并精确定位负责分泌ACTH的垂体肿瘤。即使使用磁共振成像(MRI),通常也很难获得足够的诊断信息,在这些情况下,我们依靠双侧岩下窦采血(BIPSS)。该程序被认为是诊断的金标准方法,但与任何其他诊断方法一样,它也并非没有假阳性或假阴性等错误结果。