Alba Eva L, Japp Emily A, Fernandez-Ranvier Gustavo, Badani Ketan, Wilck Eric, Ghesani Munir, Wolf Andrea, Wolin Edward M, Corbett Virginia, Steinmetz David, Skamagas Maria, Levine Alice C
The Adrenal Center, Division of Endocrine, Diabetes and Bone Diseases, Department of Medicine at the Icahn School of Medicine at Mount Sinai, New York , NY, USA.
Division of Endocrinology, Diabetes, and Nutrition, Department of Medicine at the University of Maryland School of Medicine, Baltimore, MD, USA.
J Endocr Soc. 2022 May 6;6(7):bvac073. doi: 10.1210/jendso/bvac073. eCollection 2022 Jul 1.
Neoplasms that secrete ectopic adrenocorticotropin (ACTH) may cause severe, life-threatening hypercortisolism. These tumors are often difficult to localize and treat, requiring a comprehensive and systematic management plan orchestrated by a multidisciplinary team. The Mount Sinai Adrenal Center hosted an interdisciplinary retreat of experts in adrenal disorders and neuroendocrine tumors (NETs) with the aim of developing a clinical pathway for the management of Cushing syndrome due to ectopic ACTH production. The result was institutional recommendations for the diagnosis, localization, surgical approaches to intrathoracic tumors and bilateral adrenalectomy, and perioperative and postoperative medical management of hypercortisolism and its sequelae. Specific recommendations were made regarding the timing and selection of therapies based on the considerations of our team as well as a review of the current literature. Our clinical pathway can be applied by other institutions directly or serve as a guide for institution-specific management.
分泌异位促肾上腺皮质激素(ACTH)的肿瘤可能导致严重的、危及生命的皮质醇增多症。这些肿瘤往往难以定位和治疗,需要由多学科团队精心制定全面系统的管理计划。西奈山肾上腺中心举办了一次肾上腺疾病和神经内分泌肿瘤(NETs)专家跨学科研讨会,旨在制定因异位ACTH分泌导致的库欣综合征的临床管理路径。结果形成了关于诊断、定位、胸内肿瘤的手术方法和双侧肾上腺切除术,以及皮质醇增多症及其后遗症的围手术期和术后药物管理的机构建议。基于我们团队的考虑以及对当前文献的回顾,针对治疗的时机和选择提出了具体建议。我们的临床路径可供其他机构直接应用,或作为特定机构管理的指南。