| Literature DB >> 33447578 |
Fabio Tortora1, Alberto Negro2, Francesco Briganti1, Maria Laura Del Basso De Caro3, Luigi Maria Cavallo4, Domenico Solari4, Teresa Somma4, Luca Brunese5, Ferdinando Caranci6.
Abstract
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. 2020 Gland Surgery. All rights reserved.Entities:
Keywords: Cushing’s disease (CD); bilateral inferior petrosal sinus samples; magnetic resonance imaging (MRI); microcatheter
Year: 2020 PMID: 33447578 PMCID: PMC7804552 DOI: 10.21037/gs-20-654
Source DB: PubMed Journal: Gland Surg ISSN: 2227-684X