| Literature DB >> 31036383 |
German Rubinstein1, Andrea Osswald1, Stephanie Zopp1, Katrin Ritzel1, Marily Theodoropoulou1, Felix Beuschlein2, Martin Reincke3.
Abstract
Cushing's disease (CD) is the most common etiology of Cushing's syndrome (CD) due to corticotroph pituitary adenoma, which are in most cases small (80-90% microadenomas) and in about 40% cannot be visualized on imaging of the sella. First-line treatment for CD is transsphenoidal surgery (TSS) with the aim of complete adenoma removal and preservation of pituitary gland function. As complete adenoma resection is not always possible, surgical failure is a common problem. This can be the case either due to persistent hypercortisolism after first TSS or recurrence of hypercortisolism after initially achieving remission. For these scenarios exist several therapeutic options with their inherent characteristics, which will be covered by this review.Entities:
Keywords: ACTH; adrenal steroidogenesis inhibitor; bilateral adrenalectomy; hypercortisolism; pituitary radiation; transsphenoidal surgery
Year: 2019 PMID: 31036383 DOI: 10.1016/j.beem.2019.04.004
Source DB: PubMed Journal: Best Pract Res Clin Endocrinol Metab ISSN: 1521-690X Impact factor: 4.690