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异位促肾上腺皮质激素综合征:罕见简单,却始终充满挑战。

The Ectopic Adrenocorticotropic Hormone Syndrome: Rarely Easy, Always Challenging.

机构信息

Neuroendocrine Tumour Unit, Royal Free Hospital, Pond Street, London NW3 2QG, UK.

Neuroendocrine Tumour Unit, Royal Free Hospital, Pond Street, London NW3 2QG, UK.

出版信息

Endocrinol Metab Clin North Am. 2018 Jun;47(2):409-425. doi: 10.1016/j.ecl.2018.01.005.

Abstract

Despite modern imaging techniques, differentiating ectopic adrenocorticotropic hormone (ACTH) syndrome from pituitary-dependent Cushing's syndrome, Cushing's disease, is especially difficult when well-differentiated carcinoids are the source of ACTH secretion, particularly pulmonary carcinoid tumors. ACTH-secreting pulmonary carcinoids, like the corticotroph adenomas causing Cushing's disease, are often small and difficult to detect, and patients present with a gradual onset of the classical signs and symptoms of Cushing's syndrome, indistinguishable from the presentation of Cushing's disease. Hence, the differential diagnosis relies on a combination of clinical assessment, dynamic biochemical tests, inferior petrosal sinus sampling, and multimodal imaging, each with its own caveats and pitfalls.

摘要

尽管有现代成像技术,但在区分异位促肾上腺皮质激素(ACTH)综合征与垂体依赖性库欣综合征时,特别是当 ACTH 分泌的来源是分化良好的类癌时,这种区分尤其困难,尤其是肺类癌肿瘤。像引起库欣病的促肾上腺皮质激素分泌垂体腺瘤一样,ACTH 分泌性肺类癌通常较小且难以检测,患者表现为逐渐出现库欣综合征的典型体征和症状,与库欣病的表现无法区分。因此,鉴别诊断依赖于临床评估、动态生化测试、岩下窦取样和多模态成像的综合应用,每种方法都有其自身的注意事项和陷阱。

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