Baker J, Holdaway I M, Jagusch M, Kerr A R, Donald R A, Pullan P T
J Endocrinol Invest. 1982 Jan-Feb;5(1):33-8. doi: 10.1007/BF03350479.
A 51-year old man presented with the classical features of Cushing's syndrome which had evolved over the previous 5 yr, and was found to have ACTH secretion from an atypical thymic carcinoid tumor. Tumor extract, assayed under conditions designed to prevent artefactual generation of peptides, was found to contain a wide variety of immunoreactive hormones including ACTH, alpha-MSH, CLIP, beta-endorphin and met-enkephalin. The ACTH-related peptides were probably derived from a common precursor, pro-opiocortin, but the presence of met-enkephalin suggests the production of a separate type of precursor molecule. The tumor was locally invasive and, depsite subtotal excision and radiotherapy, continued to secrete large amounts of ACTH. Hypercortisolism was controlled longterm with pharmacological adrenal blockade and steroid replacement.
一名51岁男性表现出在过去5年中逐渐发展的库欣综合征的典型特征,经检查发现其非典型胸腺类癌肿瘤分泌促肾上腺皮质激素(ACTH)。在旨在防止肽类物质人为生成的条件下对肿瘤提取物进行检测,发现其中含有多种免疫反应性激素,包括促肾上腺皮质激素、α-促黑素(α-MSH)、促肾上腺皮质激素样中叶肽(CLIP)、β-内啡肽和甲硫氨酸脑啡肽。与促肾上腺皮质激素相关的肽类物质可能源自共同的前体分子阿片促皮质素原,但甲硫氨酸脑啡肽的存在表明产生了一种单独类型的前体分子。该肿瘤具有局部侵袭性,尽管进行了次全切除和放疗,但仍继续分泌大量促肾上腺皮质激素。通过药物性肾上腺阻断和类固醇替代疗法,长期控制了高皮质醇血症。